<?xml version="1.0" encoding="utf-8"?>
<XML>
<JOURNAL>
<YEAR>2023</YEAR>
<VOL>21</VOL>
<NO>3</NO>
<MOSALSAL>0</MOSALSAL>
<PAGE_NO>267</PAGE_NO>


<ARTICLES>

	<ARTICLE> 
		<TitleF>Differences between living and deceased donation in human uterus transplantation: A narrative review</TitleF>
		<TitleE>تفاوت های اهدا زنده و مرده در پیوند رحم در انسان: یک مرور روایتی</TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>1</Language_ID>
			<CONTENT>تصمیم برای استفاده از اهداکننده زنده یا مرده برای انجام پیوند رحم، یک ارزیابی سود و زیان است و اساسا بر پایه انتخاب&#173;های تیم پزشکی می&#173;باشد. مطالعه حاضر جهت تعیین تفاوت&#173;های بین اهدا زنده و مرده در پیوند رحم در انسان بر اساس عوامل تعیین&#173;کننده در انتخاب نوع اهداکننده، طراحی شد. جهت انجام این مطالعه مروری، پایگاه اطلاعاتی PubMed بدون محدودیت زمانی، زبانی و مکانی تا می 2022 جستجو شد. از 113 مقاله شناسایی شده، 45 مقاله برای بررسی، وارد مطالعه شد. براساس نتایج، در مقایسه با اهدا زنده، بزرگترین مزیت اهدا مرده، فقدان خطرات جراحی و یا روانی برای اهداکننده می&#173;باشد. در مقابل در اهدا مرده، ارزیابی پزشکی جامع قبل از پیوند، کمتر امکان پذیر است و جراحی از قبل برنامه&#173;ریزی شده، ممکن نیست. براساس یافته&#173;های کارآزمایی&#173;های بالینی داوری شده انتشار یافته، میزان شکست گرفت در پیوند رحم با استفاده از اهداکننده زنده و مرده به ترتیب 21% و 36% می&#173;باشد. با فرض اینکه همه گیرنده&#173;هایی که شکست گرفت نداشته&#173;اند تحت انتقال جنین قرار گرفته باشند، میزان تولد زنده در پروسیجرهای پیوند رحم با استفاده از اهداکننده زنده و مرده به ترتیب تقریبا 63% و 71% می&#173;باشد. در حال حاضر با توجه به وقوع تولد زنده از هر دو نوع اهدا به ویژه از اهداکننده مرده نولی پار، افزایش تقاضا برای پیوند رحم در آینده نزدیک، کمبود گرفت&#173;های رحمی و فقدان داده کافی جهت مقایسه کامل دو نوع اهدا، استفاده از هر دو اهدا هنوز هم ضروری و منطقی به نظر می&#173;رسد.</CONTENT>
			</ABSTRACT>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>The decision to use a living or deceased donor to perform uterus transplantation (UTx) is an evaluation of benefit and harm and is based on the medical team&#8217;s choices. The current study determines the differences between living and deceased donation in human UTx according to determinant factors in choosing the donor type. For this review study, the PubMed database was searched without time, language, and location limitations up to May 2022. From 113 identified articles, 45 papers were included in the study for review. According to the results, in comparison to living donation, the biggest advantage of deceased donation is the lack of surgical and or psychological risks for the donor. In contrast, a comprehensive pre-transplantation medical assessment is less possible in deceased donation, and preplanned surgery cannot be realized. According to published peer-reviewed clinical trials on UTx, the graft failure rates in living and deceased donor UTx are 21% and 36%, respectively. Supposing all recipients who did not have graft failure underwent embryo transfer, live birth rates in living and deceased donor UTx procedures are almost 63% and 71%, respectively. Currently, considering the occurrence of live births from both donations, particularly from nulliparous deceased donor, increased demand for UTx in the near future, shortage of uterus grafts, and lack of sufficient data for a comprehensive comparison between the 2 types of donation, the use of both donations still seems necessary and rational.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>193</FPAGE>
			<TPAGE>204</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2022/07/25
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1401/5/3
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2023/01/21
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/11/1
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Sakineh</Name>
				<MidName></MidName>
				<Family>Taherkhani</Family>
				<NameE>Sakineh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Taherkhani</FamilyE>
				<Organizations>
				<Organization>School of Medicine, Arak University of Medical Sciences, Arak, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>ایران</Country>
				</Countries>
				<EMAILS>
				<Email>sakinehtaherkhani@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Living donors</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Deceased donors</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Brain death donors</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Uterus transplantation</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Absolute uterine factor infertility</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Review.</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>اهداکنندگان زنده</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>اهداکنندگان مرده</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>اهداکنندگان مرگ مغزی</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>پیوند رحم</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>نازایی رحمی مطلق</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>مطالعه مروری.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
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Ethical implications of donor type for uterus transplantation: Why we should remain wary of using living donors. Yale J Biol Med 2020; 93: 587-592.##Jones BP, Ranaei‐Zamani N, Vali S, Williams N, Saso S, Thum MY, et al. Options for acquiring motherhood in absolute uterine factor infertility; adoption, surrogacy and uterine transplantation. Obstet Gynaecol 2021; 23: 138-147.##Kvarnström N, Enskog A, Dahm-Kähler P, Brännström M. Live versus deceased donor in uterus transplantation. Fertil Steril 2019; 112: 24-27.##Fageeh W, Raffa H, Jabbad H, Marzouki A. Transplantation of the human uterus. Int J Gynecol Obstet 2002; 76: 245-251.##O'Donovan L, Williams NJ, Wilkinson S. Ethical and policy issues raised by uterus transplants. Br Med Bull 2019; 131: 19-28.##Flyckt RL, Farrell RM, Perni UC, Tzakis AG, Falcone T. Deceased donor uterine transplantation: Innovation and adaptation. Obstet Gynecol 2016; 128: 837-842.##Dickens BM. Legal and ethical issues of uterus transplantation. Int J Gynaecol Obstet 2016; 133: 125-128.##Williams N. Should deceased donation be morally preferred in uterine transplantation trials? Bioethics 2016; 30: 415-424.##Williams NJ. Deceased donation in uterus transplantation trials: Novelty, consent, and surrogate decision making. Am J Bioeth 2018; 18: 18-20.##Brännström M, Johannesson L, Bokström H, Kvarnström N, Mölne J, Dahm-Kähler P, et al. Livebirth after uterus transplantation. Lancet 2015; 385: 607-616.##https://doi.org/10.1016/S0140-6736(15)61098-4##Ejzenberg D, Andraus W, Mendes LRBC, Ducatti L, Song A, Tanigawa R, et al. Livebirth after uterus transplantation from a deceased donor in a recipient with uterine infertility. Lancet 2018; 392: 2697-2704.##Kisu I, Banno K, Matoba Y, Aoki D. Uterus transplantation: Advantages and disadvantages of a deceased donor. Arch Gynecol Obstet 2019; 299: 1213-1214.##Favre-Inhofer A, Rafii A, Carbonnel M, Revaux A, Ayoubi JM. Uterine transplantation: Review in human research. J Gynecol Obstet Hum Reprod 2018; 47: 213-221.##Akar ME, Ozkan O, Aydinuraz B, Dirican K, Cincik M, Mendilcioglu I, et al. Clinical pregnancy after uterus transplantation. Fertil Steril 2013; 100: 1358-1363.##https://doi.org/10.1016/j.fertnstert.2013.08.047##Ozkan O, Ozkan O, Dogan NU, Bahceci M, Mendilcioglu I, Boynukalin K, et al. Birth of a healthy baby 9 years after a surgically successful deceased donor uterus transplant. Ann Surg 2022; 275: 825-832.##Brännström M, Bokström H, Dahm-Kähler P, Diaz-Garcia C, Ekberg J, Enskog A, et al. One uterus bridging three generations: First live birth after mother-to-daughter uterus transplantation. Fertil Steril 2016; 106: 261-266.##Brännström M, Johannesson L, Dahm-Kähler P, Enskog A, Mölne J, Kvarnström N, et al. First clinical uterus transplantation trial: A six-month report. Fertil Steril 2014; 101: 1228-1236.##Broecker V, Brännström M, Ekberg J, Dahm‐Kähler P, Mölne J. Uterus transplantation: Histological findings in explants at elective hysterectomy. Am J Transplant 2021; 21: 798-808.##Huang Y, Ding X, Chen B, Zhang G, Li A, Hua W, et al. Report of the first live birth after uterus transplantation in People's Republic of China. Fertil Steril 2020; 114: 1108-1115.##Wei L, Xue T, Tao K-S, Zhang G, Zhao G-Y, Yu S-Q, et al. Modified human uterus transplantation using ovarian veins for venous drainage: The first report of surgically successful robotic-assisted uterus procurement and follow-up for 12 months. Fertil Steril 2017; 108: 346-356.##Flyckt R, Kotlyar A, Arian S, Eghtesad B, Falcone T, Tzakis A. Deceased donor uterine transplantation. Fertil Steril 2017; 107: e13.##Puntambekar S, Puntambekar S, Telang M, Kulkarni P, Date S, Panse M, et al. Novel anastomotic technique for uterine transplant using utero-ovarian veins for venous drainage and internal iliac arteries for perfusion in two laparoscopically harvested uteri. J Minim Invasive Gynecol 2019; 26: 628-635.##Puntambekar S, Telang M, Kulkarni P, Puntambekar S, Jadhav S, Panse M, et al. Laparoscopic-assisted uterus retrieval from live organ donors for uterine transplant: Our experience of two patients. J Minim Invasive Gynecol 2018; 25: 622-631.##https://doi.org/10.1016/j.jmig.2018.09.323##https://doi.org/10.1016/j.jmig.2018.01.009##Flyckt R, Falcone T, Quintini C, Perni U, Eghtesad B, Richards EG, et al. First birth from a deceased donor uterus in the United States: From severe graft rejection to successful cesarean delivery. Am J Obstet Gynecol 2020; 223: 143-151.##Brucker SY, Strowitzki T, Taran F-A, Rall K, Schöller D, Hoopmann M, et al. Living-donor uterus transplantation: Pre-, intra-, and postoperative parameters relevant to surgical success, pregnancy, and obstetrics with live births. J Clin Med 2020; 9: 2485.##Brännström M, Dahm-Kähler P, Ekberg J, Akouri R, Groth K, Enskog A, et al. Outcome of recipient surgery and 6-month follow-up of the Swedish live donor robotic uterus transplantation trial. J Clin Med 2020; 9: 2338.##Brännström M, Dahm‐Kähler P, Kvarnström N, Akouri R, Rova K, Olausson M, et al. Live birth after robotic‐assisted live donor uterus transplantation. Acta Obstet Gynecol Scand 2020; 99: 1222-1229.##Johannesson L, Testa G, Putman JM, McKenna GJ, Koon EC, York JR, et al. Twelve live births after uterus transplantation in the Dallas UtErus Transplant Study. Obstet Gynecol 2021; 137: 241-249.##Testa G, McKenna GJ, Bayer J, Wall A, Fernandez H, Martinez E, et al. The evolution of transplantation from saving lives to fertility treatment: DUETS (Dallas UtErus Transplant Study). Ann Surg 2020; 272: 411-417.##Fronek J, Kristek J, Chlupac J, Janousek L, Olausson M. Human uterus transplantation from living and deceased donors: The interim results of the first 10 cases of the Czech trial. J Clin Med 2021; 10: 586.##Carmona F, Rius M, Díaz-Feijoo B, Musquera M, Tort J, Alcaraz A. Uterine transplantation. First viable case in Southern Europe. Med Clin (Barc) 2021; 156: 297-300.##Vieira MA, Souza C, Nobrega L, Reis R, Andrade C, Schmidt R, et al. Uterine transplantation with robot-assisted uterus retrieval from living donor: First case in Brazil. J Minim Invasive Gynecol 2021; 28: 1817.##https://doi.org/10.1016/j.jmig.2021.08.028##Kisu I, Kato Y, Obara H, Matsubara K, Matoba Y, Banno K, et al. Emerging problems in uterus transplantation. BJOG 2018; 125: 1352-1356.##Testa G, Koon EC, Johannesson L. Living donor uterus transplant and surrogacy: Ethical analysis according to the principle of equipoise. Am J Transplant 2017; 17: 912-916.##Kisu I, Mihara M, Banno K, Umene K, Araki J, Hara H, et al. Risks for donors in uterus transplantation. Reprod Sci 2013; 20: 1406-1415.##Flyckt R, Farrell RM, Falcone T. Advancing the science of uterine transplantation: Minimizing living donor risk on a path to surgical innovation. J Minim Invasive Gynecol 2019; 26: 577-579.##Liu Y, Zhang Y, Ding Y, Chen G, Zhang X, Wang Y, et al. Clinical applications of uterus transplantation in China: Issues to take into consideration. J Obstet Gynaecol Res 2020; 46: 357-368.##Farrell RM, Falcone T. Uterine transplant: New medical and ethical considerations. Lancet 2015; 385: 581-582.##Kumnig M, Jowsey-Gregoire SG. Key psychosocial challenges in vascularized composite allotransplantation. World J Transplant 2016; 6: 91-102.##Gomel V. Uterine transplantation. Climacteric 2019; 22: 117-121.##Hammond‐Browning N. UK criteria for uterus transplantation: A review. BJOG 2019; 126: 1320-1326.##https://doi.org/10.1111/1471-0528.15909##Johannesson L, Dahm-Kahler P, Eklind S, Brannstrom M. The future of human uterus transplantation. Women's Health 2014; 10: 455-467.##Kisu I, Banno K, Mihara M, Suganuma N, Aoki D. Current status of uterus transplantation in primates and issues for clinical application. Fertil Steril 2013; 100: 280-294.##Lefkowitz A, Edwards M, Balayla J. The montreal criteria for the ethical feasibility of uterine transplantation. Transpl Int 2012; 25: 439-447.##Guntram L, Williams NJ. Positioning uterus transplantation as a 'more ethical' alternative to surrogacy: Exploring symmetries between uterus transplantation and surrogacy through analysis of a Swedish government white paper. Bioethics 2018; 32: 509-518.##Testa G, Johannesson L. The ethical challenges of uterus transplantation. Curr Opin Organ Transplant 2017; 22: 593-597.##Hammond-Browning N, Yao SL. Deceased donation uterus transplantation: A review. Transplantology 2021; 2: 140-148.##Bruno B, Arora KS. Uterus transplantation: The ethics of using deceased versus living donors. Am J Bioeth 2018; 18: 6-15.##https://doi.org/10.1080/15265161.2018.1478018##Brucker SY, Brännström M, Taran F-A, Nadalin S, Königsrainer A, Rall K, et al. Selecting living donors for uterus transplantation: Lessons learned from two transplantations resulting in menstrual functionality and another attempt, aborted after organ retrieval. Arch Gynecol Obstet 2018; 297: 675-684.##Matoba Y, Kisu I, Banno K, Aoki D. Operative and clinical outcomes of minimally invasive living-donor surgery on uterus transplantation: A literature review. J Clin Med 2021; 10: 349.##Taherkhani S. [Ethical considerations in domestic violence related researches]. J Med Ethics 2016; 10: 141-175. (In Persian)##Ozkan O, Akar ME, Ozkan O, Erdogan O, Hadimioglu N, Yilmaz M, et al. Preliminary results of the first human uterus transplantation from a multiorgan donor. Fertil Steril 2013; 99: 470-476.##Dion L, Santin G, Nyangoh Timoh K, Boudjema K, Jacquot Thierry L, Gauthier T, et al. Procurement of uterus in a deceased donor multi-organ donation national program in France: A scarce resource for uterus transplantation? J Clin Med 2022; 11: 730.##Chmel R, Pastor Z, Novackova M, Matecha J, Cekal M, Fronek J. Clinical pregnancy after deceased donor uterus transplantation: Lessons learned and future perspectives. J Obstet Gynaecol Res 2019; 45: 1458-1465.##Tardieu A, Dion L, Lavoue V, Chazelas P, Marquet P, Piver P, et al. The key role of warm and cold ischemia in uterus transplantation: A review. J Clin Med 2019; 8: 760.##Ngaage LM, Ike S, Elegbede A, Vercler CJ, Gebran S, Liang F, et al. The changing paradigm of ethics in uterus transplantation: A systematic review. Transpl Int 2020; 33: 260-269.##Jones BP, Saso S, Quiroga I, Yazbek J, Smith JR. Re: UK criteria for uterus transplantation: A review. BJOG 2019; 126: 1507-1508.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Uterine artery Doppler and endometrial blood flow in frozen embryo transfer: A cohort study</TitleF>
		<TitleE>داپلر شریان رحم و جریان خون آندومتر در انتقال جنین منجمد: یک مطالعه مشاهده‌ای</TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>1</Language_ID>
			<CONTENT>مقدمه: میزان لانه &#173;گزینی پس از فناوری کمک باروری (ART) به دو عامل مهم بستگی دارد: جنین با کیفیت خوب و پذیرش آندومتر. پذیرش آندومتر عمدتاً با اندازه&#173;گیری اولتراسوند ضخامت و مورفولوژی آندومتر ارزیابی می&#173;شود.
هدف: این مطالعه با هدف بررسی رابطه بین شاخص&#173;های داپلر شریان رحمی / پرفیوژن آندومتر و میزان بارداری انجام شد.
مواد و روش&#173; ها: این مطالعه مشاهده&#8204;ای آینده&#8204;نگر بر روی 250 زن کاندید انتقال جنین در چرخه انتقال جنین منجمد از ژانویه 2022 تا ژولای 2022 انجام شد. برای ارزیابی پذیرش آندومتر، سونوگرافی داپلر رحم قبل از جنین انجام شد. انتقال با آندومتر با ظاهر مطلوب (ضخامت آندومتر بیشتر یا مساوی 7 میلی&#173;متر و خط سه&#173;گانه. علاوه بر این، بیماران بر اساس حاملگی بالینی به دو گروه مثبت و منفی تقسیم شدند و شاخص&#173;های شریان رحمی و پرفیوژن آندومتر بین این گروه&#173;ها مقایسه شد).
نتایج: داپلر شریان رحمی نشان داد که شاخص ضربان بین دو گروه مثبت و منفی حاملگی بالینی تفاوت معنی&#8204;داری دارد، اما شاخص مقاومت و حداکثر سرعت سیستولیک از نظر آماری تفاوت معنی&#8204;داری با هم ندارند. همچنین پرفیوژن آندومتر بین دو گروه حاملگی بالینی تفاوت معنی&#173;داری داشت. پرفیوژن آندومتر در &#160;&#160;&#160;گروه&#173;های حاملگی بالینی مثبت به طور معنی&#173;داری بهتر بود.
نتیجه&#173; گیری: سونوگرافی داپلر ابزاری مفید برای ارزیابی پذیرش آندومتر است.
&#160;</CONTENT>
			</ABSTRACT>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: The implantation rate after assisted reproductive technology depends on 2 important factors, good quality embryo and endometrial receptivity. Endometrial receptivity is mainly assessed by ultrasound measurement of endometrial thickness and morphology.
Objective: This study aimed to investigate the relationship between uterine artery Doppler indices/endometrial perfusion and pregnancy rate.
Materials and Methods: This cohort study was done on 250 women who were candidates for frozen embryo transfer from January to July 2022. For assessing endometrial receptivity, we performed a Doppler ultrasound of the uterus before embryo transfer with apparently desirable endometrium (endometrial thickness &#8805; 7 mm and 3 line endometrial pattern). In addition, the women were divided into 2 groups according to assisted reproductive technology outcome (clinical pregnancy), group I positive clinical pregnancy, and group II negative clinical pregnancy, and uterine artery indices and endometrial perfusion were compared between these groups.
Results: Uterine artery Doppler showed that the pulsatility index was significantly different between positive and negative clinical pregnancy groups, but resistance index and peak systolic velocity (PSV) did not have statistically significant differences. Also, endometrial perfusion was significantly different between the 2 groups of clinical pregnancy. Endometrial perfusion was significantly better in positive clinical pregnancy groups. 
Conclusion: Doppler ultrasound can help to assess endometrial receptivity.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>205</FPAGE>
			<TPAGE>212</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2022/07/252022/10/25
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1401/8/3
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2023/01/212023/01/21
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/11/1
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Fereshteh</Name>
				<MidName></MidName>
				<Family>Bahrami</Family>
				<NameE>Fereshteh</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Bahrami</FamilyE>
				<Organizations>
				<Organization>Research and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>ایران</Country>
				</Countries>
				<EMAILS>
				<Email>fereshtehbahrami1966@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Maryam</Name>
				<MidName></MidName>
				<Family>Eftekhar</Family>
				<NameE>Maryam</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Eftekhar</FamilyE>
				<Organizations>
				<Organization>Research and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>ایران</Country>
				</Countries>
				<EMAILS>
				<Email>eftekharmaryam@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Leila</Name>
				<MidName></MidName>
				<Family>Zanbagh</Family>
				<NameE>Leila</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Zanbagh</FamilyE>
				<Organizations>
				<Organization>Department of Obstetrics and Gynecology, Afshar Hospital, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>ایران</Country>
				</Countries>
				<EMAILS>
				<Email>javadkhataie@gmail.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Doppler ultrasonography</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Embryo transfer</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Assisted reproductive technology</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Pregnancy.</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>داپلر</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>انتقال جنین</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>فناوری کمک باروری</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>بارداری.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Kim A, Jung H, Choi WJ, Hong SN, Kim HY. Detection of endometrial and subendometrial vasculature on the day of embryo transfer and prediction of pregnancy during fresh in vitro fertilization cycles. Taiwan J Obstet Gynecol 2014; 53: 360-365.##Zebitay AG, Tutumlu M, Verit FF, Ilhan GK, Gungor ES, Cetin O, et al. A comparative analysis of arterial blood flow in unexplained infertility, tubal infertility and fertile groups. Gynecol Endocrinol 2016; 32: 442-445.##Crosby DA, Glover LE, Downey P, Mooney EE, McAuliffe FM, O'Farrelly C, et al. Mid-luteal uterine artery Doppler indices in the prediction of pregnancy outcome in nulliparous women undergoing assisted reproduction. Hum Fertil 2022; 25: 670-676.##Sardana D, Upadhyay AJ, Deepika K, Pranesh GT, Rao KA. Correlation of subendometrial-endometrial blood flow assessment by two-dimensional power Doppler with pregnancy outcome in frozen-thawed embryo transfer cycles. J Hum Reprod Sci 2014; 7: 130-135.##El-Mazny A, Abou-Salem N, ElShenoufy H. Doppler study of uterine hemodynamics in women with unexplained infertility. Eur J Obstet Gynecol Reprod Biol 2013; 171: 84-87.##Singh N, Bahadur A, Mittal S, Malhotra N, Bhatt A. Predictive value of endometrial thickness, pattern and sub-endometrial blood flows on the day of hCG by 2D doppler in in-vitro fertilization cycles: A prospective clinical study from a tertiary care unit. J Hum Reprod Sci 2011; 4: 29-33.##Ali zarad C, Mohamed MH, Shanab WSA. Role of uterine artery Doppler in assessment of unexplained infertility. Egypt J Radiol Nuclear Med 2021; 52: 59.##Moramezi F, Barati M, Mosavi Mobarakeh M. A comparative study of uterine artery blood flow in patients with unexplained infertility and normal fertile women using Doppler sonography. Int J Pharm Res Allied Sci 2016; 5: 221-228.##Makhija K, Shrivasatava D, Tiwari M. Predictive value of uterine artery: Peak systolic velocity on the day of trigger for clinical pregnancy rate in infertile women. Int J Reprod Contracept Obstet Gynecol 2019; 8: 677-682.##Maged AM, Kamel AM, Abu-Hamila F, Elkomy RO, Ohida OA, Hassan SM, et al. The measurement of endometrial volume and sub-endometrial vascularity to replace the traditional endometrial thickness as predictors of in-vitro fertilization success. Gynecol Endocrinol 2019; 35: 949-954.##Riad ON, Hak AA. Assessment of endometrial receptivity using Doppler ultrasonography in infertile women undergoing intrauterine insemination. Gynecol Endocrinol 2014; 30: 70-73.##Khan MS, Shaikh A, Ratnani R. Ultrasonography and Doppler study to predict uterine receptivity in infertile patients undergoing embryo transfer. J Obstet Gynecol India 2016; 66 (Suppl.): 377-382.##Adibi A, Khadem M, Mardanian F, Hovsepian S. Uterine and arcuate arteries blood flow for predicting of ongoing pregnancy in in vitro fertilization. J Res Med Sci 2015; 20: 879-884.##Prasad S, Goyal R, Kumar Y, Nayar P, Hajela S, Kumaran A, et al. The relationship between uterine artery two-dimensional color Doppler measurement and pregnancy outcome: A prospective observational study. J Reprod Infertil 2017; 18: 251-256.##Ivanovski M, Damcevski N, Radevska B, Doicev G. Assessment of uterine artery and arcuate artery blood flow by transvaginal color Doppler ultrasound on the day of human chorionic gonadotropin administration as predictors of pregnancy in an in vitro fertilization program. Akush Ginekol (Sofiia) 2012; 51: 55-60.##Zollner U, Specketer MT, Zollner KP, Dietl J. Uterine artery blood flow in the periimplantation period in embryo transfer cycles. Asian Pac J Reprod 2012; 1: 177-182.##Abdel Kader M, Abdelmeged A, Mahran A, Abu Samra MF, Bahaa H. The usefulness of endometrial thickness, morphology and vasculature by 2D Doppler ultrasound in prediction of pregnancy in IVF/ICSI cycles. Egypt J Radiol Nuclear Med 2016; 47: 341-346.##Nandi A, Martins WP, Jayaprakasan K, Clewes JS, Campbell BK, Raine-Fenning NJ. Assessment of endometrial and subendometrial blood flow in women undergoing frozen embryo transfer cycles. Reprod BioMed Online 2014; 28: 343-351.##Mayer RB, Ebner T, Weiss C, Allerstorfer C, Altmann R, Oppelt P, et al. The role of endometrial volume and endometrial and subendometrial vascularization parameters in a frozen embryo transfer cycle. Reprod Sci 2019; 26: 1013-1018.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Trans differentiating human adipose-derived mesenchymal stem cells into male germ-like cells utilizing Rabbit Sertoli cells: An experimental study</TitleF>
		<TitleE>تمایز سلول‌های بنیادی مزانشیمی مشتق از چربی انسانی به سلول‌های شبه زایایی نر با استفاده از سلول‌های سرتولی خرگوش: یک مطالعه تجربی</TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>1</Language_ID>
			<CONTENT>مقدمه: سلول&#173;های بنیادی مزانشیمی (MSCs) به عنوان عوامل درمانی جدید بالقوه برای درمان ناباروری در نظر گرفته می&#173;شوند و بافت چربی (AT) به منبع بالقوه سلول&#173;های بنیادی مزانشیمی تبدیل شده است. برای هدایت صحیح سلول&#173;های بنیادی مزانشیمی در فرآیند تمایز، یک محیط مشابه با محیط in vivo ممکن است ضروری باشد.
هدف: این مطالعه با هدف تمایز MSc مشتق از AT انسانی (hAD-MScs) به سلول&#8204;های شبه زایایی نر در شرایط آزمایشگاهی با استفاده از ترکیبی از محیط تهیه &#8204;شده با سلول&#8204;های سرتولی خرگوش (SCCM)، پروتئین مورفوژنتیک استخوان 4 و اسید رتینوئیک انجام شد.
مواد و روش &#173;ها: MSc ها از &#160;ATهای انسانی اهداکنندگان بارور و نابارور جداسازی شدند. &#160;MScهای تأیید شده با استفاده از یک پروتکل 2 مرحله&#173;ای متمایز شدند. مرحله اول شامل ng/ml 20 پروتئین مورفوژنتیک استخوان 4 بود. مرحله دوم با استفاده از &#181;m 1 رتینوئیک اسید و/یا SCCM انجام شد. تغییرات مورفولوژیکی و بیان نشانگرهای اختصاصی سلول زایا (GC) شامل فاکتور رونویسی باند اکتامر-4، تحریک شده توسط رتینوئیک اسید-8، پروتئین کمپلکس سیناپتونمال-3، و پروتامین-1 در سلول&#173;های تیمار شده با استفاده از واکنش زنجیره&#173;ای پلیمراز کمی ارزیابی شدند.
نتایج: القای hAD-MScs منجر به افزایش بیان ژن&#8204;های اختصاصی GC شد که در این میان تیمار SCCM بالاترین میزان بیان را نشان داد. بیان ژن&#173;های پروتئین-3 و پروتامین-1 کمپلکس سیناپتونمال به ترتیب پس از 19 و 26 روز از القاء شناسایی شد. PRM1 در hAD-MScs کشت شده در SCCM زودتر از سایر گروه&#8204;های تیمار شده شناسایی شد. سلول&#8204;های تیمار شده دوک&#8204;های درازتری را نشان دادند و با هم توده&#8204;هایی را تشکیل دادند.
نتیجه &#173;گیری: hAD-MScs های تمایز یافته به دودمان GC توانایی بیان نشانگرهای اختصاصی GC را در شرایط آزمایشگاهی نشان دادند و سلول&#8204;های سرتولی خرگوش را می&#8204;توان برای القای تمایز hAD-MScs به سلول&#8204;های شبه زایایی استفاده کرد.</CONTENT>
			</ABSTRACT>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Mesenchymal stem cells (MSCs) are deemed as potential new therapeutic agents for infertility treatment and adipose tissue (AT) becomes a potential MSCs source. To direct MSCs through the differentiation process properly, an environment comparable to the in vivo niche might be indispensable.
Objective: This study aims to differentiate human AT-derived MScs (hAD-MScs) into male germ-like cells in vitro using a combination of rabbit Sertoli cells conditioned medium (SCCM), bone morphogenetic protein 4, and retinoic acid.
Materials and Methods: MScs were isolated from human ATs of fertile and infertile donors. The verified MScs were differentiated using a 2-step protocol; the first step included 20 ng/ml bone morphogenetic protein 4 treatment. The second step was performed utilizing 1 &#956;M retinoic acid and/or SCCM. The morphological changes and the expression of germ cell (GC)-specific markers: octamer-binding transcription factor-4; stimulated by retinoic-acid-8, synaptonemal complex protein-3, and protamine-1 were assessed in the treated cells using quantitative polymerase chain reaction. 
Results: Induction of hAD-MScs resulted in the upregulation of GC-specific genes where SCCM treatment showed the highest expression. The synaptonemal complex protein-3 and protamine-1 gene expression was detected after 19 and 26 days of induction, respectively. PRM1 was detected in hAD-MScs cultured in SCCM earlier than in other treated groups. The treated cells became more elongated-like spindles and formed aggregates.
Conclusion: hAD-MScs differentiated to GC lineage exhibited the ability to express GC-specific markers under in vitro conditions, and rabbit&#8217;s Sertoli cells can be used for inducing transdifferentiation of hAD-MScs into germ-like cells.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>213</FPAGE>
			<TPAGE>228</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2022/07/252022/10/252022/08/31
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1401/6/9
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2023/01/212023/01/212023/01/23
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/11/3
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Alaa Mutee'</Name>
				<MidName></MidName>
				<Family>Khudair</Family>
				<NameE>Alaa Mutee'</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Khudair</FamilyE>
				<Organizations>
				<Organization>Medical Laboratory Sciences Department, Faculty of Health Sciences, Islamic University of Gaza, Gaza City, Palestine.</Organization>
				</Organizations>
				<Countries>
				<Country>فلسطین</Country>
				</Countries>
				<EMAILS>
				<Email>akhudair@iugaza.edu.ps</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mazen Medhat</Name>
				<MidName></MidName>
				<Family>Alzaharna</Family>
				<NameE>Mazen Medhat</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Alzaharna</FamilyE>
				<Organizations>
				<Organization>Medical Laboratory Sciences Department, Faculty of Health Sciences, Islamic University of Gaza, Gaza City, Palestine.</Organization>
				</Organizations>
				<Countries>
				<Country>فلسطین</Country>
				</Countries>
				<EMAILS>
				<Email>mzaharna@iugaza.edu.ps</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Fadel Akram</Name>
				<MidName></MidName>
				<Family>Sharif</Family>
				<NameE>Fadel Akram</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sharif</FamilyE>
				<Organizations>
				<Organization>Medical Laboratory Sciences Department, Faculty of Health Sciences, Islamic University of Gaza, Gaza City, Palestine.</Organization>
				</Organizations>
				<Countries>
				<Country>فلسطین</Country>
				</Countries>
				<EMAILS>
				<Email>fsharif@iugaza.edu.ps</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Adipose tissue-derived mesenchymal stem cell</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Bone morphogenetic protein 4</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Germ-line cells</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Retinoic acid</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Sertoli cells.</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>سلول های بنیادی مزانشیمی مشتق از بافت چربی</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>پروتئین مورفوژنتیک استخوان 4</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>سلول های زایا</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>رتینوئیک اسید</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>سلول های سرتولی.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Ghaem Maghami R, Mirzapour T, Bayrami A. Differentiation of mesenchymal stem cells to germ‐like cells under induction of Sertoli cell‐conditioned medium and retinoic acid. Andrologia 2018; 50: e12887.##Nagamatsu G, Hayashi K. Stem cells, in vitro gametogenesis and male fertility. Reproduction 2017; 154: F79-F91.##Zhankina R, Baghban N, Askarov M, Saipiyeva D, Ibragimov A, Kadirova B, et al. Mesenchymal stromal/stem cells and their exosomes for restoration of spermatogenesis in non-obstructive azoospermia: A systemic review. Stem Cell Res Ther 2021; 12: 229.##Mouka A, Tachdjian G, Dupont J, Drévillon L, Tosca L. In vitro gamete differentiation from pluripotent stem cells as a promising therapy for infertility. Stem Cells Dev 2016; 25: 509-521.##Majidi F, Bamehr H, Shalchian Z, Kouchakian MR, Mohammadzadeh N, Khalili A. Differentiation of human umbilical cord mesenchymal stem cell into germ‐like cell under effect of co‐culture with testicular cell tissue. Anat Histol Embryol 2020; 49: 359-364.##De Felici M. The formation and migration of primordial germ cells in mouse and man. Molecular mechanisms of cell differentiation in gonad development. Cham: Springer; 2016.##Irie N, Sybirna A, Surani MA. What can stem cell models tell us about human germ cell biology? Curr Top Dev Biol 2018; 129: 25-65.##Madeja ZE, Pawlak P, Piliszek A. Beyond the mouse: Non-rodent animal models for study of early mammalian development and biomedical research. Int J Dev Biol 2019; 63: 187-201.##Banco B, Grilli G, Giudice C, Tomas Marques A, Cotti Cometti S, Visigalli G, et al. Immunophenotyping of rabbit testicular germ and Sertoli cells across maturational stages. J Histochem Cytochem 2016; 64: 715-726.##Grieco V, Banco B. Rabbit sertoli cells: Immunohistochemical profile from neonatal to adult age. Methods Mol Biol 2018; 1748: 37-47.##Ziaeipour S, Ahrabi B, Naserzadeh P, Aliaghaei A, Sajadi E, Abbaszadeh H-A, et al. Effects of Sertoli cell transplantation on spermatogenesis in azoospermic mice. Cell Physiol Biochem 2019; 52: 421-434.##Afsartala Z, Rezvanfar MA, Hodjat M, Tanha S, Assadollahi V, Bijangi K, et al. Amniotic membrane mesenchymal stem cells can differentiate into germ cells in vitro. In Vitro Cell Dev Biol Anim 2016; 52: 1060-1071.##Volarevic V, Bojic S, Nurkovic J, Volarevic A, Ljujic B, Arsenijevic N, et al. Stem cells as new agents for the treatment of infertility: Current and future perspectives and challenges. Biomed Res Int 2014; 2014: 507234.##Choudhery MS, Badowski M, Muise A, Pierce J, Harris DT. Donor age negatively impacts adipose tissue-derived mesenchymal stem cell expansion and differentiation. J Transl Med 2014; 12: 8.##Camilleri ET, Gustafson MP, Dudakovic A, Riester SM, Garces CG, Paradise CR, et al. Identification and validation of multiple cell surface markers of clinical-grade adipose-derived mesenchymal stromal cells as novel release criteria for good manufacturing practice-compliant production. Stem Cell Res Ther 2016; 7: 107.##Liu H, Chen M, Liu L, Ren S, Cheng P, Zhang H. Induction of human adipose-derived mesenchymal stem cells into germ lineage using retinoic acid. Cell Reprogram 2018; 20: 127-134.##Ghatreh Samani K, Eliyasi Dashtaki M, Alaei Sh, Saki Gh. Differentiation potential of adipose tissue‐derived mesenchymal stem cells into germ cells with and without growth factors. Andrologia 2021; 53: e13892.##Bräunig P, Glanzner WG, Rissi VB, Gonçalves PBD. The differentiation potential of adipose tissue-derived mesenchymal stem cells into cell lineage related to male germ cells. Arq Bras Med Vet Zootec 2018; 70: 160-168.##Bakhmet EI, Tomilin AN. Key features of the POU transcription factor Oct4 from an evolutionary perspective. Cell Mol Life Sci 2021; 78: 7339-7353.##Lee W-Y, Lee R, Park H-J, Do JT, Park C, Kim J-H, et al. Characterization of male germ cell markers in canine testis. Anim Reprod Sci 2017; 182: 1-8.##Jodar M, Oliva R. Protamine alterations in human spermatozoa. Genetic damage in human spermatozoa. New York: Springer; 2014.##Liu Y, Niu M, Yao C, Hai Y, Yuan Q, Liu Y, et al. Fractionation of human spermatogenic cells using STA-PUT gravity sedimentation and their miRNA profiling. Sci Rep 2015; 5: 8084.##Dissanayake D, Patel H, Wijesinghe PS. Differentiation of human male germ cells from Wharton's jelly-derived mesenchymal stem cells. Clin Exp Reprod Med 2018; 45: 75-81.##Ma Z, Qin M, Liang H, Chen R, Cai S, Huang Z, et al. Primary cilia-dependent signaling is involved in regulating mesenchymal stem cell proliferation and pluripotency maintenance. J Mol Histol 2020; 51: 241-250.##Mayère C, Neirijnck Y, Sararols P, Rands CM, Stévant I, Kühne F, et al. Single cell transcriptomics reveal temporal dynamics of critical regulators of germ cell fate during mouse sex determination. FASEB J 2021; 35: e21452.##Guo J, Grow EJ, Mlcochova H, Maher GJ, Lindskog C, Nie X, et al. The adult human testis transcriptional cell atlas. Cell Res 2018; 28: 1141-1157.##Ghorbanlou M, Abdanipour A, Shirazi R, Malekmohammadi N, Shokri S, Nejatbakhsh R. Indirect co-culture of testicular cells with bone marrow mesenchymal stem cells leads to male germ cell-specific gene expressions. Cell J 2019; 20: 505-512.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Is sperm telomere length altered in teratozoospermia specimens? A case-control study</TitleF>
		<TitleE>آیا طول تلومر اسپرم در نمونه های تراتواسپرمیا دچار تغییر می گردد؟ یک مطالعه مورد-شاهدی</TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>1</Language_ID>
			<CONTENT>مقدمه: ناباروری مردان به عنوان یک نقص چندعاملی شناخته شده است و بسیاری از دلایل آن ناشناخته است. تراتواسپرمی به عنوان یکی از نواقص در شاخصه&#173; های مایع منی به وسیله وجود بیش از 85% اسپرماتوزوا غیرطبیعی از نظر مورفولوژی در نمونه مایع منی تعریف می&#173;شود که در پیشبرد باروری نیز ناتوان هستند. یکی از جدیدترین موضوعات در مطالعات تغییرات ژنتیکی، بررسی تغییرات طول تلومر اسپرم&#173;ها و نقش آنها در ناباروری مردان است. مطالعه&#173;ی حال حاضر بر ارزیابی تغییرات طول تلومر در تراتواسپرمی تمرکز دارد.
هدف: بررسی هر گونه تفاوتی در طول تلومر بین نمونه&#173; های تراتواسپرمی و نرمال.
مواد و روش&#173; ها: در این مطالعه مورد-شاهدی، 60 مرد مراجعه&#173;کننده به کلینیک باروری اراک، بین نوامبر 2017 تا فوریه 2018 در دو دسته تراتواسپرمی و نورمواسپرمی طبقه&#173;بندی گردیدند. استخراج DNA ژنوم اسپرم صورت گرفته و سپس طول تلومر با استفاده از تکنیک qPCR مورد ارزیابی قرار گرفت.
نتایج: ارزیابی&#173;های آماری طول نسبی تلومر توسط محاسبه نسبت تلومر به ژن تک کپی برای نمونه&#173;های تراتواسپرمی و نرمال انجام گرفت. نتایج به صورت &#160;معنا&#173;داری نشان دادند که طول نسبی تلومر در نمونه&#173;های تراتواسپرمی تقریبا 3 برابر کوتاه&#173;تر از نمونه&#173;های نرمال هستند (001/ 0&#62; p).
نتیجه &#173;گیری: طول تلومر یکی از مواردی است که اخیرا در حوزه&#173;ی فاکتورهای زیستی مؤثر بر ویژگی&#173;های مایع منی مورد توجه قرار گرفته. نتایج مطالعه حال حاضر، کاهش طول تلومر در تراتواسپرمی را نشان می&#173;دهند و پیشنهاد می&#173;کند که این تغییرات ممکن است یکی از فاکتورهای مشارکت&#173;کننده در عدم کفایت این نوع از نمونه&#173;ها باشد. به هر صورت شناسایی فرایند&#173;های مولکولی مرتبط نیاز به مطالعات دقیق بیشتری خواهد داشت.</CONTENT>
			</ABSTRACT>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Male factor infertility is a multifactorial defect, and many of its etiologies are unknown. Teratozoospermia is determined by the existence of over 85% morphologically abnormal spermatozoa in semen which are almost incompetent in fertilization function. One of the most novel issues in genetic alterations studies is the variation of sperm telomere lengths (STL) and its collaboration with male infertility. The present study has been focused on STL alterations in teratozoospermia.
Objective: Investigation of differences in telomere length of teratozoospermia specimens and sperms with normal parameters.
Materials and Methods: In this case-control study, 60 men referred to Arak Fertility Clinic, Markazi province, Iran from November 2017 to February 2018 were categorized into teratozoospermia and normozoospermic groups. Sperm genomic DNA extraction was conducted, and STL were evaluated using quantitative polymerase chain reaction.
Results: Statistical evaluation of relative telomere length was calculated by the ratio of telomere to single-copy gene for teratozoospermia and normal specimens. Results significantly demonstrated that relative telomere length in teratozoospermia samples is nearly 3 times shorter than in normal samples (p &#62;0.001).
Conclusion: Our results represent the reduction of telomeres length in teratozoospermia and suggest that this alteration might be one of the factors contributing to the sperm fertility potential of this kind of specimen. However, defining relevant molecular processes requires further detailed investigations.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>229</FPAGE>
			<TPAGE>236</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2022/07/252022/10/252022/08/312021/08/13
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/5/22
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2023/01/212023/01/212023/01/232023/02/1
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/11/12
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Maryam</Name>
				<MidName></MidName>
				<Family>Fattahi</Family>
				<NameE>Maryam</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Fattahi</FamilyE>
				<Organizations>
				<Organization>Department of Medical Genetics, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>ایران</Country>
				</Countries>
				<EMAILS>
				<Email>Fattahi.inbox@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mohadese</Name>
				<MidName></MidName>
				<Family>Maghsudlu</Family>
				<NameE>Mohadese</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Maghsudlu</FamilyE>
				<Organizations>
				<Organization>Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>ایران</Country>
				</Countries>
				<EMAILS>
				<Email>m.maghsudlu.2@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Mohammad Hasan</Name>
				<MidName></MidName>
				<Family>Sheikhha</Family>
				<NameE>Mohammad Hasan</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Sheikhha</FamilyE>
				<Organizations>
				<Organization>Abortion Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.</Organization>
				</Organizations>
				<Countries>
				<Country>ایران</Country>
				</Countries>
				<EMAILS>
				<Email>sheikhha@yahoo.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Telomere</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Teratozoospermia</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Sperm</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Male infertility.</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>طول تلومر</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>تراتواسپرمی</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>اسپرم</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>ناباروری مردان.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Duca Y, Calogero AE, Cannarella R, Condorelli RA, La Vignera S. Current and emerging medical therapeutic agents for idiopathic male infertility. Exp Opin Pharmacother 2019; 20: 55-67.##Agarwal A, Baskaran S, Parekh N, Cho C-L, Henkel R, Vij S, et al. Male infertility. Lancet 2021; 397: 319-333.##Leaver RB. Male infertility: An overview of causes and treatment options. Br J Nurs 2016; 25: S35-S40.##De Braekeleer M, Nguyen MH, Morel F, Perrin A. Genetic aspects of monomorphic teratozoospermia: A review. J Assist Reprod Genet 2015; 32: 615-623.##Ammar O, Mehdi M, Muratori M. Teratozoospermia: Its association with sperm DNA defects, apoptotic alterations, and oxidative stress. Andrology 2020; 8: 1095-1106.##Beurois J, Cazin C, Kherraf Z-E, Martinez G, Celse T, Touré A, et al. Genetics of teratozoospermia: Back to the head. Best Pract Res Clin Endocrinol Metab 2020; 34: 101473.##Kim HJ, Yoon HJ, Jang JM, Oh HS, Lee YJ, Lee WD, et al. Comparison between intracytoplasmic sperm injection and intracytoplasmic morphologically selected sperm injection in oligo-astheno-teratozoospermia patients. Clin Exp Reprod Med 2014; 41: 9-14.##Ozturk S. Telomerase activity and telomere length in male germ cells. Biol Reprod 2015; 92: 53.##Miyamoto T, Minase G, Shin T, Ueda H, Okada H, Sengoku K. Human male infertility and its genetic causes. Reprod Med Biol 2017; 16: 81-88.##Lu W, Zhang Y, Liu D, Songyang Z, Wan M. Telomeres-structure, function, and regulation. Exp Cell Res 2013; 319: 133-141.##Shay JW, Wright WE. Telomeres and telomerase: Three decades of progress. Nat Rev Genet 2019; 20: 299-309.##Darmishonnejad Z, Tavalaee M, Izadi T, Tanhaei S, Nasr-Esfahani MH. Evaluation of sperm telomere length in infertile men with failed/low fertilization after intracytoplasmic sperm injection. Reprod Biomed Online 2019; 38: 579-587.##Kalmbach KH, Antunes DMF, Dracxler RC, Knier TW, Seth-Smith ML, Wang F, et al. Telomeres and human reproduction. Fertil Steril 2013; 99: 23-29.##Rocca MS, Foresta C, Ferlin A. Telomere length: Lights and shadows on their role in human reproduction. Biol Reprod 2019; 100: 305-317.##Boniewska-Bernacka E, Pańczyszyn A, Cybulska N. Telomeres as a molecular marker of male infertility. Hum Fertil 2019; 22: 78-87.##Thilagavathi J, Kumar M, Mishra S, Venkatesh S, Kumar R, Dada R. Analysis of sperm telomere length in men with idiopathic infertility. Arch Gynecol Obstet 2013; 287: 803-807.##Cawthon RM. Telomere measurement by quantitative PCR. Nucleic Acids Res 2002; 30: e47.##Boniewska-Bernacka E, Pańczyszyn A, Cybulska N. Sperm telomere length in men with normal and abnormal semen parameters. A pilot study. Biomed J Sci Tech Res 2019; 21: 15639-15645.##Ferlin A, Rampazzo E, Rocca MS, Keppel S, Frigo AC, De Rossi A, et al. In young men sperm telomere length is related to sperm number and parental age. Hum Reprod 2013; 28: 3370-3376.##Mishra SS, Kumar S, Singh G, Mohanty K, Vaid S, Malhotra N, et al. Oxidative DNA damage in male germ cells in normozoospermic infertile men: A case for concern. Austin J Reprod Med Infertil 2015; 2: 1017.##Cariati F, Jaroudi S, Alfarawati S, Raberi A, Alviggi C, Pivonello R, et al. Investigation of sperm telomere length as a potential marker of paternal genome integrity and semen quality. Reprod Biomed Online 2016; 33: 404-411.##Berneau SC, Shackleton J, Nevin C, Altakroni B, Papadopoulos G, Horne G, et al. Associations of sperm telomere length with semen parameters, clinical outcomes and lifestyle factors in human normozoospermic samples. Andrology 2020; 8: 583-593.##Liu SY, Zhang C-J, Peng H-Y, Huang X-Q, Sun H, Lin K-Q, et al. [Association study of telomere length with idiopathic male infertility]. Yi Chuan 2015; 37: 1137-1142. (in Chinese)##Biron-Shental T, Wiser A, Hershko-Klement A, Markovitch O, Amiel A, Berkovitch A. Sub-fertile sperm cells exemplify telomere dysfunction. J Assist Reprod Genet 2018; 35: 143-148.##Kurjanowicz P. Evaluation of telomere length in spermatozoa as a diagnostic tool for male factor infertility [Ph.D. thesis]. Toronto: University of Toronto (Canada) ProQuest Dissertations Publishing;  2022.##Vyas N, Gamit K, Raval M. Male infertility: A major problem worldwide and its management in ayurveda. Pharma Science Monitor 2018; 9: 446-469.##Practice Committee of the American Society for Reproductive Medicine. Diagnostic evaluation of the infertile female: A committee opinion. Fertil Steril 2015; 103: e44-e50.##Edition F. Examination and processing of human semen. Geneva: World Health Organization Press; 2010.##Agarwal A, Tvrda E, Sharma R. Relationship amongst teratozoospermia, seminal oxidative stress and male infertility. Reprod Biol Endocrinol 2014; 12: 45.##Krausz C, Riera-Escamilla A. Genetics of male infertility. Nat Rev Urol 2018; 15: 369-384.##Podlevsky JD, Chen JJ-L. It all comes together at the ends: Telomerase structure, function, and biogenesis. Mutat Res 2012; 730: 3-11.##Reig-Viader R, Garcia-Caldés M, Ruiz-Herrera A. Telomere homeostasis in mammalian germ cells: A review. Chromosoma 2016; 125: 337-351.##Balmori C, Varela E. Should we consider telomere length and telomerase activity in male factor infertility? Curr Opin Obstet Gynecol 2018; 30: 197-202.##Jørgensen PB, Fedder J, Koelvraa S, Graakjaer J. Age-dependence of relative telomere length profiles during spermatogenesis in man. Maturitas 2013; 75: 380-385.##Long J, Huang C, Chen Y, Zhang Y, Shi S, Wu L, et al. Telomeric TERB1-TRF1 interaction is crucial for male meiosis. Nat Struct Mol Biol 2017; 24: 1073-1080.##De Frutos C, López-Cardona AP, Balvís NF, Laguna-Barraza R, Rizos D, Gutierrez-Adán A, et al. Spermatozoa telomeres determine telomere length in early embryos and offspring. Reproduction 2016; 151: 1-7.##Fice HE, Robaire B. Telomere dynamics throughout spermatogenesis. Genes 2019; 10: 525.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Anti-fertility effect of Aerva lanata crude extract in male Dams offspring: An experimental study</TitleF>
		<TitleE>اثر ضد باروری عصاره خام Aerva lanata در فرزندان نر رت های حامله: یک مطالعه تجربی</TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>1</Language_ID>
			<CONTENT>مقدمه: Aerva lanata، گیاهی است که به عنوان غذا استفاده می&#173;شود و همچنین با عنوان تقویتی توسط زنان باردار برای تسکین درد معده و جلوگیری از سقط جنین مصرف می&#173;شود. این گیاه علاوه بر سایر خواص مشخصه، دارای فعالیت&#173;های ضد باروری و ضد لانه&#173;گزینی است.
هدف: این مطالعه به بررسی سمیت بر روی بیضه فرزندان رت&#173;های تیمار شده با عصاره آبی خام Aerva lanata می&#173;پردازد.
مواد و روش &#173;ها: 25 سر موش صحرایی باردار ویستار با وزن 180 تا 240 گرم به طور تصادفی در 5 گروه (هر کدام 5 سر) قرار گرفتند. گروه A به عنوان کنترل انتخاب شد. گروه&#173;های B، C، D و E به ترتیب 200، 400، 800 و 1000 میلی&#173;گرم به ازای هر کیلوگرم وزن بدن عصاره Aerva lanata را از روز 12 تا 19 بارداری دریافت کردند. نوزادان (به دنیا آمده از رت&#173;ها) وزن شدند، تحت نظر گرفته شدند و 6 هفته پس از زایمان قربانی شدند. بیضه&#173;های توله&#173;های نر برای انجام مراحل بافت&#173;شناسی به دست آمد و بافت&#173;شناسی بیضه مورد بررسی قرار گرفت.
نتایج: هیچ ناهنجاری فاحشی در گروه&#8204;های مورد آزمایش مشاهده نشد، تعداد توله&#8204;ها به&#8204;طور معنی&#8204;داری در گروه E کاهش یافت (01/0 = p)، آنالیز وزن نوزادان کاهش معنی&#8204;داری را در گروه&#8204;های C و E نشان داد (به ترتیب 04/0 = p و 02/0 =p ). میانگین وزن بیضه&#173;های توله&#173;ها در گروه&#173;های B، C، D و E (به ترتیب 03/0، 03/0، 01/0 و 001/0 &#62;) به طور قابل توجهی در مقایسه با گروه کنترل کاهش یافته بود. از نظر بافت&#173;شناسی، بافت&#173;های بیضه توله&#173;های تیمار شده درجات مختلفی از اختلال و به هم ریختگی ترتیب سلولی اپیتلیوم ژرمینال را به شیوه&#173;ای وابسته به دوز در مقایسه با گروه کنترل نشان دادند.
نتیجه &#173;گیری: این مطالعه سمیت بر روی بیضه و احتمالاً نقش ضد باروری Aerva lanata را در نوزادان رت&#173;ها نشان داد.</CONTENT>
			</ABSTRACT>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Aerva lanata, a herb used as food and also consumed as a tonic by pregnant women to relieve stomach pains and prevent miscarriage. In addition to other characterized properties, it possesses antifertility and anti-implantation activities.
Objective: This study investigates the testicular toxicity of the testes of offsprings of Dams treated with crude aqueous extract of Aerva lanata.
Materials and Methods: 25 pregnant Wistar rats (Dams) weighing 180-240 gr were randomly earmarked into 5 groups (n = 5/each). Group A served as control; groups B, C, D, and E received 200, 400, 800, and 1000 mg/kg body weight of Aerva lanata extract, respectively, beginning from 12th to 19th day of gestation. The pups (delivered of Dams) were weighed, observed, and sacrificed 6 wk post-parturition. The testes of the male pups were obtained for histological procedures the testis histology was examined.
Results: No gross malformation was observed in the treatment groups, the number of pups/litter was significantly reduced in group E (p = 0.01), pups weight analysis showed a significant reduction in groups C and E (p = 0.04, and 0.02 respectively), and the mean pup testes weight was significantly reduced in groups B, C, D, and E (p = 0.03, 0.03, 0.01, and &#60; 0.001 respectively) when compared with control. Histologically, the treated pup testes tissues showed varying degrees of disruption and distortion of the cellular arrangements of the germinal epithelium in a dose dependent manner compared to the control.
Conclusion: The study revealed a testicular toxicity and possibly antifertility role of Aerva lanata in dams&#8217; pups.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>237</FPAGE>
			<TPAGE>244</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2022/07/252022/10/252022/08/312021/08/132021/08/19
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/5/28
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2023/01/212023/01/212023/01/232023/02/12023/01/23
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/11/3
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Raphael Eguono</Name>
				<MidName></MidName>
				<Family>Uwejigho</Family>
				<NameE>Raphael Eguono</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Uwejigho</FamilyE>
				<Organizations>
				<Organization>Department of Anatomy, Faculty of Basic Medical Sciences, University of Medical Sciences, Ondo State, Laje Campus, Ondo City, Ondo State, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>نیجریه</Country>
				</Countries>
				<EMAILS>
				<Email>ruwejigho@unimed.edu.ng</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Kingsley Afoke</Name>
				<MidName></MidName>
				<Family>Iteire</Family>
				<NameE>Kingsley Afoke</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Iteire</FamilyE>
				<Organizations>
				<Organization>Department of Anatomy, Faculty of Basic Medical Sciences, University of Medical Sciences, Ondo State, Laje Campus, Ondo City, Ondo State, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>نیجریه</Country>
				</Countries>
				<EMAILS>
				<Email>aiteire@unimed.edu.ng</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Felix Udawmojo</Name>
				<MidName></MidName>
				<Family>Enemali</Family>
				<NameE>Felix Udawmojo</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Enemali</FamilyE>
				<Organizations>
				<Organization>Department of Anatomy, Faculty of Basic Medical Sciences, University of Medical Sciences, Ondo State, Laje Campus, Ondo City, Ondo State, Nigeria.</Organization>
				</Organizations>
				<Countries>
				<Country>نیجریه</Country>
				</Countries>
				<EMAILS>
				<Email>fenamali@unimed.edu.ng</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Amaranthaceae</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Fertility</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Male fertility</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Male reproductive system</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Local herbs.</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>تاج خروس</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>باروری</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>باروری نر</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>دستگاه تناسلی نر</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>گیاهان محلی.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Hao D-C. Ranunculales medicinal plants: Biodiversity, chemodiversity and pharmacotherapy. UK: Academic Press; 2019.##Mintah SO, Asafo-Agyei T, Archer MA, Atta-Adjei Junior P, Boamah D, Kumadoh D, et al. Medicinal plants for treatment of prevalent diseases. In: Perveen Sh, Al-Taweel A. Pharmacognosy: Medicinal plants. UK: Intechopen; 2018.##Akunne TC, Uzor Ph, Onyeto CA, Okereke EK. Safe African Medicinal plants for clinical studies. In: Kuete V. Toxicological survey of African Medicinal plants. London: Elsevier; 2014: 535-555.##Karemore MN, Avari JG. Herbal medicines used during pregnancy, childbirth and postpartum care. Int J Pharm Sci Res 2017; 8: 5326-5335.##Musaddiqa S, Mustafaa K, Ahmadb S, Aslama S, Alic B, Khakwania S, et al. Pharmaceutical, ethnopharmacological, phytochemical and synthetic importance of genus Aerva: A review. Natural Product Communications 2018; 13: 375-385.##Zhao Y, Kumar D, Prasad DN, Singhb RK, Ma Y. Morphoanatomic, physicochemical, and phytochemical standardization with HPTLC fingerprinting of aerial parts of Aerva lanata (Linn) Juss ex schult. J Trad Chinese Med Sci 2015; 2: 39-44.##Savadi RV, Alagawadi KR. Antifertility activity of ethanolic extracts of plumbago indica and Aerva lanata on albino rats. Int J Green Pharmcol 2009; 3: 230-233.##Carlson B. Human embryology and developmental biology. 5th Ed. Philadelphia: Saunders; 2013.##Costa KCS, Bezerra SB, Norte CM, Nunes LMN, de Olinda TM. Medicinal plants with teratogenic potential: Current considerations. Braz J Pharm Sci 2012; 48: 427-433.##Ghuman S, Coopoosamy RM. Crude sample preparation, extraction and in vitro screening for antimicrobial activity of selected wound healing medicinal plants in KwaZulu-Natal, South Africa: A review. J Med Plant Res 2011; 5: 3572-3576.##Kpemissi M, Eklu-Gadegbeku K, Veerapur VP, Potârniche AV, Adi K, Vijayakumar S, et al. Antioxidant and nephroprotection activities of Combretum micranthum: A phytochemical, in-vitro and ex-vivo studies. Heliyon 2019; 5: e01365.##Kpemissi M, Eklu-Gadegbeku K, Veerapur VP, Negru M, Taulescu M, Chandramohan V, et al. Nephroprotective activity of Combretum micranthum G. Don in cisplatin induced nephrotoxicity in rats: In-vitro, in-vivo and in-silico experiments. Biomed Pharmacother 2019; 116: 108961.##Ema M, Miyawaki E, Kawashima K. Critical period for adverse effects on development of reproductive system in male offspring of rats given di-n-butyl phthalate during late pregnancy. Toxicol Lett 2000; 111: 271-278.##Picut CA, Remick AK, de Rijk EP, Simons ML, Stump DG, Parker GA. Postnatal development of the testis in the rat: Morphologic study and correlation of morphology to neuroendocrine parameters. Toxicol Pathol 2015; 43: 326-342.##https://doi.org/10.1177/0192623314547279##Shields VDC, Heinbockel Th. Introductory chapter: Histological microtechniques. In: Heinbockel Th, Shields VDC. Histology. UK: IntechOpen; 2018.##Ankul SS, Gowri K, Chitra V. A review on phytochemical constituents and pharmacological activities of the plant: Aerva Lanata. Res J Pharm Technol 2020; 13: 1580-1586.##Weichbrod RH, Thompson GAH, Norton JN. Management of animal care and use programs in research, education, and testing. 2nd Ed. Boca Raton (FL): CRC Press/Taylor &#38; Francis; 2018.##Athira P, Nair SN. Pharmacognostic review of medicinal plant Aerva lanata. J Pharn Sci Res 2017; 9: 1420-1423.##Omotoso KS, Aigbe FR, Salako OA, Chijioke MC, Adeyemi OO. Toxicological evaluation of the aqueous whole plant extracts of Aerva lanata Juss. ex Schult (Amaranthaceae). J Ethnopharmacol 2017; 208: 174-184.##Bitasta M, Madan S. Aerva lanata: A blessing of mother nature. J Pharmacogn Phytochem 2016; 5: 92-101.##Shaik A, Yalavarthi PR, Bannoth CK. Role of anti-fertility medicinal plants on male &#38; female reproduction. J Complement Altern Med Res 2017; 3: 1-22.##Daniyal M, Akram M. Antifertility activity of medicinal plants. J Chinese Med Assoc 2015; 78: 382-388.##Oduwole OO, Peltoketo H, Huhtaniemi IT. Role of follicle-stimulating hormone in spermatogenesis. Front Endocrinol 2018; 9: 763.##O'Shaughnessy PJ, Fowler PA. Endocrinology of the mammalian fetal testis. Reproduction 2011; 141: 37-46.##D'Cruz SC, Vaithinathan S, Jubendradass R, Mathur PP. Effects of plants and plant products on testis. Asian J Androl 2010; 12: 468-479.##Dewal S, Sharma R, Gupta RS. A review on antifertility activities of plants of Chambal riverine. Asian J Pharm Clini Res 2018; 11: 8-14.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Live birth rates in day 5 fresh versus vitrified single blastocyst transfer cycles: A cross-sectional analysis</TitleF>
		<TitleE>نرخ تولد زنده در چرخه های انتقال بلاستوسیست منفرد تازه در روز 5 در مقابل انتقال منجمد: یک مطالعه مقطعی</TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>1</Language_ID>
			<CONTENT>مقدمه: استفاده از انتقال جنین منجمد (FET) در فرآیندهای کمک به تولید&#173;مثل در سراسر جهان افزایش یافته است. تحریک کنترل شده تخمدان و سپس انتقال جنین تازه ممکن است همزمانی آندومتر و جنین را مختل کند. با این حال، شواهد متناقضی در مورد نرخ تولد زنده (LBR) و نرخ حاملگی بالینی (CPR) وجود دارد.
هدف: مقایسه LBRs و CPRs در چرخه&#8204;های انتقال بلاستوسیست تازه اتولوگ منفرد روز 5 در مقابل سیکل&#8204;های انتقال بلاستوسیست منجمد شده، برای بررسی تأثیر تحریک کنترل &#8204;شده تخمدان بر ناهمزمانی جنین-آندومتر.
مواد و روش &#173;ها: یک تجزیه و تحلیل مقطعی بزرگ از 6002 انتقال جنین (ET) شامل 3774 چرخه تازه و 2228 چرخه FET از سال 2016 تا 2019 انجام شد. در ضمن تجزیه و تحلیل چند متغیره و زیر گروهی برای پاسخ&#8204;دهندگان بالا (بیش از 20 تخمک) انجام شد.
نتایج: تجزیه و تحلیل تک متغیره تفاوتی در LBR و CPR نشان نداد. با این حال، تجزیه و تحلیل چند متغیره کاهش قابل توجهی در LBR و CPR در FET در مقایسه با انتقال امبریوهای تازه نشان داد. سن شرکت&#8204;کننده جوان&#8204;تر، سابقه حاملگی در لقاح آزمایشگاهی قبلی، گسترش بلاستوسیست پیشرفته، تروفکتودرم با کیفیت بالاتر و تعداد تجمعی کمتر ETs همگی شانس LBR و CPR را بهبود بخشیدند. لقاح آزمایشگاهی معمولی، به جای تزریق داخل سیتوپلاسمی اسپرم، CPR را بهبود بخشید اما LBR را بهبود نبخشید. شاخص توده بدنی LBR و CPR را تحت تأثیر قرار نداد. در زیر گروه مطالعه شده تجزیه و تحلیل چند متغیره پاسخ&#173;دهندگان بالا تفاوتی در LBR یا CPR نشان نداد.
نتیجه &#173;گیری: این مطالعه با تحلیل چند متغیره نشان می&#8204;دهد که LBR و CPR در ETs تازه نسبتاً در حدود 14% بالاتر در مقایسه با FETs می&#173;باشد. یک استراتژی یکسان انجماد، بدون دلیل مناسب، ممکن است به نتایج نامطلوب منجر شود. در افراد با پاسخ&#8204;دهی بالا، چرخه&#8204;های فریز کردن ممکن است مفید باشد، در عین حال نتایج مشابه به نظر می&#8204;رسد.</CONTENT>
			</ABSTRACT>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: The use of frozen embryo transfers (FET) in assisted reproduction has increased worldwide. Controlled ovarian hyperstimulation in a fresh transfer may impair endometrial-embryo synchronicity. However, there is conflicting evidence on live birth rates (LBR) and clinical pregnancy rates (CPR).
Objective: To compare LBRs and CPRs between single autologous day 5 fresh vs. vitrified blastocyst transfer cycles, to investigate the impact of controlled ovarian hyperstimulation on embryo-endometrium asynchrony.
Materials and Methods: A large cross-sectional analysis of 6002 embryo transfers (ET) comprised 3774 fresh and 2228 FET cycles from 2016 to 2019. Multivariate and subgroup analysis were performed for high responders (&#62; 20 oocytes).
Results: Univariate analysis showed no difference in LBR (28.3% vs. 27.4%, p = 0.43) and CPR (32.2% vs. 30.9%, p = 0.30); however, multivariate analysis demonstrated significantly lower LBR (OR 0.864, p = 0.046, 95% CI 0.749-0.997) and CPR (OR 0.852, p = 0.024, 95% CI 0.742-0.979) in FET compared to fresh ETs. Younger participant age, previous in vitro fertilization pregnancy, advanced blastocyst expansion, higher trophectoderm quality, and lower cumulative number of ETs all improved the odds of LBR and CPR. Conventional in vitro fertilization, rather than intracytoplasmic sperm injection, improved CPR but not LBR. Body mass index affected neither LBR nor CPR. In the subgroup, multivariate analysis of high responders showed no difference in LBR or CPR. 
Conclusion: This study demonstrates relatively higher LBR and CPR of nearly 14% for fresh ETs compared to FETs, in multivariate analysis. A universal freeze-all strategy, without appropriate indication, may lead to suboptimal outcomes. In high responders, freeze-all cycles may be beneficial, as outcomes appear similar.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>245</FPAGE>
			<TPAGE>254</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2022/07/252022/10/252022/08/312021/08/132021/08/192022/07/10
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1401/4/19
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2023/01/212023/01/212023/01/232023/02/12023/01/232023/02/14
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/11/25
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Violet</Name>
				<MidName></MidName>
				<Family>Kieu</Family>
				<NameE>Violet</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Kieu</FamilyE>
				<Organizations>
				<Organization>Reproductive Services Unit, Royal Women’s Hospital, Melbourne, VIC, Australia. Department of Obstetrics and Gynaecology, The University of Melbourne, Melbourne, VIC, Australia. Melbourne IVF, Melbourne, VIC, Australia.</Organization>
				</Organizations>
				<Countries>
				<Country>استرالیا</Country>
				</Countries>
				<EMAILS>
				<Email>violet.kieu@unimelb.edu.au</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Alex</Name>
				<MidName></MidName>
				<Family>Polyakov</Family>
				<NameE>Alex</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Polyakov</FamilyE>
				<Organizations>
				<Organization>Reproductive Services Unit, Royal Women’s Hospital, Melbourne, VIC, Australia. Department of Obstetrics and Gynaecology, The University of Melbourne, Melbourne, VIC, Australia. Melbourne IVF, Melbourne, VIC, Australia.</Organization>
				</Organizations>
				<Countries>
				<Country>استرالیا</Country>
				</Countries>
				<EMAILS>
				<Email>alex.polyakov@mivf.com.au</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Genia</Name>
				<MidName></MidName>
				<Family>Rozen</Family>
				<NameE>Genia</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Rozen</FamilyE>
				<Organizations>
				<Organization>Reproductive Services Unit, Royal Women’s Hospital, Melbourne, VIC, Australia. Department of Obstetrics and Gynaecology, The University of Melbourne, Melbourne, VIC, Australia. Melbourne IVF, Melbourne, VIC, Australia.</Organization>
				</Organizations>
				<Countries>
				<Country>استرالیا</Country>
				</Countries>
				<EMAILS>
				<Email>genia.rozen@mivf.com.au</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Daniel</Name>
				<MidName></MidName>
				<Family>Lantsberg</Family>
				<NameE>Daniel</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Lantsberg</FamilyE>
				<Organizations>
				<Organization>Reproductive Services Unit, Royal Women’s Hospital, Melbourne, VIC, Australia. Department of Obstetrics and Gynaecology, The University of Melbourne, Melbourne, VIC, Australia. Melbourne IVF, Melbourne, VIC, Australia.</Organization>
				</Organizations>
				<Countries>
				<Country>استرالیا</Country>
				</Countries>
				<EMAILS>
				<Email>daniel.lantsberg@mivf.com.au</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Catharyn</Name>
				<MidName></MidName>
				<Family>Stern</Family>
				<NameE>Catharyn</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Stern</FamilyE>
				<Organizations>
				<Organization>Reproductive Services Unit, Royal Women’s Hospital, Melbourne, VIC, Australia. Department of Obstetrics and Gynaecology, The University of Melbourne, Melbourne, VIC, Australia. Melbourne IVF, Melbourne, VIC, Australia.</Organization>
				</Organizations>
				<Countries>
				<Country>استرالیا</Country>
				</Countries>
				<EMAILS>
				<Email>kate.stern@mivf.com.au</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Wan Tinn</Name>
				<MidName></MidName>
				<Family>The</Family>
				<NameE>Wan Tinn</NameE>
				<MidNameE></MidNameE>
				<FamilyE>The</FamilyE>
				<Organizations>
				<Organization>Reproductive Services Unit, Royal Women’s Hospital, Melbourne, VIC, Australia. Department of Obstetrics and Gynaecology, The University of Melbourne, Melbourne, VIC, Australia. Melbourne IVF, Melbourne, VIC, Australia.</Organization>
				</Organizations>
				<Countries>
				<Country>استرالیا</Country>
				</Countries>
				<EMAILS>
				<Email>wantinn.teh@mivf.com.au</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Blastocyst</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Live birth</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>In vitro techniques</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Pregnancy rate</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Vitrification</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Reproduction.</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>بلاستوسیست</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>تولد زنده</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>تکنیک­های آزمایشگاهی</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>میزان بارداری</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>انجماد</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>تولید­مثل.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Newman JE, Paul RC, Chambers GM. Assisted reproductive technology in Australia and New Zealand 2019. Sydney: University of New South Wales; 2021.##Harris K, Fitzgerald O, Paul RC, Macaldowie A, Lee E, Chambers GM. Assisted reproductive technology in Australia and New Zealand 2014. Sydney: National Perinatal Epidemiology and Statistics Unit, the University of New South Wales; 2016.##Wyns C, Bergh C, Calhaz-Jorge C, De Geyter C, Kupka MS, Motrenko T, et al. ART in Europe, 2016: Results generated from European registries by ESHRE. Hum Reprod Open 2020; 2020: hoaa032.##CDC Centers for Disease Control and Prevention. 2016 Assisted Reproductive Technology National Summary Report. Atlanta (GA): US Dept of Health and Human Services; 2018.##Ishihara O, Jwa SC, Kuwahara A, Ishikawa T, Kugu K, Sawa R, et al. Assisted reproductive technology in Japan: A summary report for 2016 by the Ethics Committee of the Japan Society of Obstetrics and Gynecology. Reprod Med Biol 2018; 18: 7-16.##Rienzi L, Gracia C, Maggiulli R, LaBarbera AR, Kaser DJ, Ubaldi FM, et al. Oocyte, embryo and blastocyst cryopreservation in ART: Systematic review and meta-analysis comparing slow-freezing versus vitrification to produce evidence for the development of global guidance. Hum Reprod Update 2017; 23: 139-155.##Kolibianakis E, Bourgain C, Albano C, Osmanagaoglu K, Smitz J, Van Steirteghem A, et al. Effect of ovarian stimulation with recombinant follicle-stimulating hormone, gonadotropin releasing hormone antagonists, and human chorionic gonadotropin on endometrial maturation on the day of oocyte pick-up. Fertil Steril 2002; 78: 1025-1029.##Mirkin S, Nikas G, Hsiu JG, Diaz J, Oehninger S. Gene expression profiles and structural/functional features of the peri-implantation endometrium in natural and gonadotropin-stimulated cycles. J Clin Endocrinol Metab 2004; 89: 5742-5752.##Meyer WR, Novotny DB, Fritz MA, Beyler SA, Wolf LJ, Lessey BA. Effect of exogenous gonadotropins on endometrial maturation in oocyte donors. Fertil Steril 1999; 71: 109-114.##Seif MW, Pearson JM, Ibrahim ZH, Buckley CH, Aplin JD, Buck P, et al. Endometrium in in-vitro fertilization cycles: Morphological and functional differentiation in the implantation phase. Hum Reprod 1992; 7: 6-11.##Venetis CA, Kolibianakis EM, Bosdou JK, Lainas GT, Sfontouris IA, Tarlatzis BC, et al. Basal serum progesterone and history of elevated progesterone on the day of hCG administration are significant predictors of late follicular progesterone elevation in GnRH antagonist IVF cycles. Hum Reprod 2016; 31: 1859-1865.##Shapiro BS, Daneshmand ST, Garner FC, Aguirre M, Hudson C, Thomas S. Evidence of impaired endometrial receptivity after ovarian stimulation for in vitro fertilization: A prospective randomized trial comparing fresh and frozen-thawed embryo transfers in high responders. Fertil Steril 2011; 96: 516-518.##https://doi.org/10.1016/j.fertnstert.2011.02.059##Bosdou JK, Venetis CA, Tarlatzis BC, Grimbizis GF, Kolibianakis EM. Higher probability of live-birth in high, but not normal, responders after first frozen-embryo transfer in a freeze-only cycle strategy compared to fresh-embryo transfer: A meta-analysis. Hum Reprod 2019; 34: 491-505.##Stormlund S, Sopa N, Zedeler A, Bogstad J, Praetorius L, Nielsen HS, et al. Freeze-all versus fresh blastocyst transfer strategy during in vitro fertilisation in women with regular menstrual cycles: Multicentre randomised controlled trial. BMJ 2020; 370: m2519.##Wei D, Liu JY, Sun Y, Shi Y, Zhang B, Liu JQ, et al. Frozen versus fresh single blastocyst transfer in ovulatory women: A multicentre, randomised controlled trial. Lancet 2019; 393: 1310-1318.##Zaat T, Zagers M, Mol F, Goddijn M, van Wely M, Mastenbroek S. Fresh versus frozen embryo transfers in assisted reproduction. Cochrane Database Syst Rev 2021; 2: CD011184.##Teh WT, Polyakov A, Garrett C, Edgar D, Mcbain J, Rogers PAW. Reduced live birth rates in frozen versus fresh single cleavage stage embryo transfer cycles: A cross-sectional study. Int J Reprod BioMed 2020; 18: 491-500.##Smith ADAC, Tilling K, Lawlor DA, Nelson SM. Live birth rates and perinatal outcomes when all embryos are frozen compared with conventional fresh- and frozen-embryo transfer: A cohort study of 337,148 in vitro fertilisation cycles. BMC Med 2019; 17: 202.##Maheshwari A, Bell JL, Bhide P, Brison D, Child T, Chong HY, et al. Elective freezing of embryos versus fresh embryo transfer in IVF: A multicentre randomized controlled trial in the UK (E-Freeze). Hum Reprod 2022; 37: 476-487.##Aflatoonian A, Karimzadeh Maybodi MA, Aflatoonian N, Tabibnejad N, Amir-Arjmand MH, Soleimani M, et al. Perinatal outcome in fresh versus frozen embryo transfer in ART cycles. Int J Reprod BioMed 2016; 14: 167-172.##Glujovsky D, Quinteiro Retamar AM, Alvarez Sedo CR, Ciapponi A, Cornelisse S, Blake D. Cleavage stage versus blastocyst stage embryo transfer in assisted reproductive technology. Cochrane Database Syst Rev 2022; 5: CD002118.##Gardner DK, Schoolcraft WB. In vitro culture of human blastocysts. In: Jansen R, Mortimer D. Toward reproductive certainty: Fertility and genetics beyond. UK: Parthenon Publishing; 1999: 378-388.##Gardner DK, Lane M, Stevens J, Schlenker T, Schoolcraft WB. Blastocyst score affects implantation and pregnancy outcome: Towards a single blastocyst transfer. Fertil Steril 2000; 73: 1155-1158.##World Health Organization. ICD-10: International statistical classification of diseases and related health problem: 10th version. 2nd Ed. Switzerland: World Health Organization Press; 2004.##Gat I, Shlush E, Quach K, Librach CL. The continuum of high ovarian response: A rational approach to the management of high responder patient subgroups. Syst Biol Reprod Med 2015; 61: 336-344.##Ferraretti AP, Gianaroli L, Magli C, Fortini D, Selman HA, Feliciani E. Elective cryopreservation of all pronucleate embryos in women at risk of ovarian hyperstimulation syndrome: Efficiency and safety. Hum Reprod 1999; 14: 1457‐1460.##Pakes C, Volovsky M, Rozen G, Agresta F, Gardner DK, Polyakov A. Comparing pregnancy outcomes between natural cycles and artificial cycles following frozen-thaw embryo transfers. Aust N Z J Obstet Gynaecol 2020; 60: 804-809.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>Determination of serum anti-Mullerian hormone levels in a low-prognosis women treated in-vitro fertilization/intracytoplasmic sperm injection: A cohort study</TitleF>
		<TitleE>تعیین سطح سرمی آنتی مولرین هورمون در زنان با پیش آگهی پایین تحت درمان لقاح آزمایشگاهی/تزریق داخل سیتوپلاسمی اسپرم: یک مطالعه کوهورت</TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>1</Language_ID>
			<CONTENT>مقدمه: پیش&#8204;بینی نتیجه درمان افراد تحت درمان با لقاح آزمایشگاهی یا تزریق داخل سیتوپلاسمی اسپرم (IVF/ICSI) با استفاده از غلظت هورمون آنتی&#173;مولرین (AMH) به طور گسترده&#173;ای مورد استفاده قرار گرفته است. با توجه به راهبردهای بیمار محور که شامل تعریف تعداد تخمک فردی (POSEIDON) است، پاسخ&#173;دهندگان ضعیف یا poor معیار بولونیا به افراد با پیش&#173;آگهی پایین تغییر کرده&#173;اند. این معیار پیش آگهی پایین را به 4 گروه تقسیم می&#173;کند.
هدف: هدف از این مطالعه بررسی سطح AMH خون در گروه زنان تحت درمان با IVF/ICSI بود که به نظر می&#173;رسید که پیش&#8204;آگهی پایینی داشته باشند.
مواد و روش &#173;ها: یک مطالعه کوهورت گذشته&#8204;نگر بین 252 شرکت&#8204;کننده مشکوک به قرار گرفتن در گروه با پیش آگهی پایین از ژانویه 2016 تا دسامبر 2019 در Morula IVF، بیمارستان ملی، سورابایا، اندونزی انجام شد. سطوح سرمی AMH و میزان بارداری مشاهده شده در بین 4 زیر گروه مقایسه شد.
نتایج: مقدار cutoff AMH با حساسیت 7/86% و اختصاصیت 70%، ng/ml 7/1 برای تشخیص زنان با پیش&#173;آگهی پایین با استفاده از معیارهای POSEIDON بود. تفاوتی در میزان بارداری بین تمام گروه&#173;ها وجود نداشت (05/0 &#60; p).
نتیجه گیری: سطوح AMH مطابق با دستورالعمل&#8204;های POSEIDON ممکن است نشان&#8204;دهنده پیش آگهی ضعیف برای زنانی که IVF/ICSI دارند، باشد. برای پیش&#8204;بینی پیش&#8204;آگهی بد در زنان، مقدار cutoff باید مشخص شود.</CONTENT>
			</ABSTRACT>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Outcome prediction of participants treated with in-vitro fertilization or intracytoplasmic sperm injection (IVF/ICSI) using anti-Mullerian hormone (AMH) concentration has been widely used. According to the patient-oriented strategies encompassing individualized oocyte number (POSEIDON) definition, low prognosis Bologna responders have changed from poor. This definition divides low prognosis into 4 groups.
Objective: The purpose of this study was to assess blood AMH levels in the group of women treated with IVF/ICSI who were thought to have a low prognosis.
Materials and Methods: A retrospective cohort study among 252 suspected low-prognosis group participants was assessed between January 2016 and December 2019 at Morula IVF, National hospital, Surabaya, Indonesia. Observed AMH serum levels and pregnancy rates were compared among 4 subgroups.
Results: The AMH cutoff value was 1.7 ng/mL with a sensitivity of 86.7 percent and a specificity of 70% for diagnosing low-prognosis women using POSEIDON criteria. There was no difference in the pregnancy rate between those groups (p &#62; 0.05).
Conclusion: AMH levels may indicate a poor prognosis for women having IVF/ICSI in accordance with POSEIDON guidelines. To predict the poor prognosis in women, the cutoff value must be identified.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>255</FPAGE>
			<TPAGE>262</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2022/07/252022/10/252022/08/312021/08/132021/08/192022/07/102021/11/11
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1400/8/20
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2023/01/212023/01/212023/01/232023/02/12023/01/232023/02/142023/02/14
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/11/25
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Ferdy Royland</Name>
				<MidName></MidName>
				<Family>Marpaung</Family>
				<NameE>Ferdy Royland</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Marpaung</FamilyE>
				<Organizations>
				<Organization>Department of Clinical Pathology, Faculty of Medicine, Dr Soetomo Academic Hospital, Universitas Airlangga, Surabaya, Indonesia.</Organization>
				</Organizations>
				<Countries>
				<Country>اندونزی</Country>
				</Countries>
				<EMAILS>
				<Email>ferdyoke@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Amang Surya</Name>
				<MidName></MidName>
				<Family>Priyanto</Family>
				<NameE>Amang Surya</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Priyanto</FamilyE>
				<Organizations>
				<Organization>IVF Morula Clinic, National Hospital Surabaya, Indonesia.</Organization>
				</Organizations>
				<Countries>
				<Country>اندونزی</Country>
				</Countries>
				<EMAILS>
				<Email>amangsuryap2@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Fitri Ayu</Name>
				<MidName></MidName>
				<Family>Kusumawati</Family>
				<NameE>Fitri Ayu</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Kusumawati</FamilyE>
				<Organizations>
				<Organization>IVF Morula Clinic, National Hospital Surabaya, Indonesia.</Organization>
				</Organizations>
				<Countries>
				<Country>اندونزی</Country>
				</Countries>
				<EMAILS>
				<Email>fitriayukusumawati2@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Sidarti</Name>
				<MidName></MidName>
				<Family>Soehita</Family>
				<NameE>Sidarti</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Soehita</FamilyE>
				<Organizations>
				<Organization>Department of Clinical Pathology, Faculty of Medicine, Dr Soetomo Academic Hospital, Universitas Airlangga, Surabaya, Indonesia.</Organization>
				</Organizations>
				<Countries>
				<Country>اندونزی</Country>
				</Countries>
				<EMAILS>
				<Email>r-sidarti-s-s@fk.unair.ac.id</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Aryati</Name>
				<MidName></MidName>
				<Family>Aryati</Family>
				<NameE>Aryati</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Aryati</FamilyE>
				<Organizations>
				<Organization>Department of Clinical Pathology, Faculty of Medicine, Dr Soetomo Academic Hospital, Universitas Airlangga, Surabaya, Indonesia.</Organization>
				</Organizations>
				<Countries>
				<Country>اندونزی</Country>
				</Countries>
				<EMAILS>
				<Email>aryati@fk.unair.ac.id</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Prognosis</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Assisted reproductive technics</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Gonadal hormone</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Fertilization in vitro</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Reproductive health.</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>پیش ­آگهی</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>تکنیک­های کمک باروری</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>هورمون غدد جنسی</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>لقاح آزمایشگاهی</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>سلامت باروری.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Kresna A, Lestari TD, Kasman AM, Luqman EM. Calcium ionophore as oocyte activator to fertilization rate and cleavage level on kacang goat post intracytoplasmic sperm injection (ICSI). Teikyo Med J 2021; 44: 1031-1037.##Rahayu FK, Dwiningsih SR, Sa'adi A, Herawati L. Effects of different intensities of exercise on folliculogenesis in mice: Which is better? Clin Exp Reprod Med 2021; 48: 43-49.##Mohammadzadeh M, Fesahat F, Khoradmehr A, Khalili MA. Influential effect of age on oocyte morphometry, fertilization rate and embryo development following IVF in mice. Middle East Fertil Soc J 2018; 23: 117-120.##Leijdekkers JA, Eijkemans MJC, van Tilborg TC, Oudshoorn SC, van Golde RJT, Hoek A, et al. Cumulative live birth rates in low-prognosis women. Hum Reprod 2019; 34: 1030-1041.##Lukaszuk K, Liss J, Kunicki M, Jakiel G, Wasniewski T, Woclawek-Potocka I, et al. Anti-Müllerian hormone (AMH) is a strong predictor of live birth in women undergoing assisted reproductive technology. Reprod Biol 2014; 14: 176-181.##Alanazi H, Bushaqer N, Ayyoub H, Dayoub N, Hassan S. Antimullerian hormone (AMH) level and IVF/ICSI cycle outcome in expected poor responders. Middle East Fertil Soc J 2018; 23: 246-250.##Ferraretti AP, Gianaroli L. The Bologna criteria for the definition of poor ovarian responders: Is there a need for revision? Hum Reprod 2014; 29: 1842-1845.##Esteves SC, Roque M, Bedoschi GM, Conforti A, Humaidan P, Alviggi C. Defining low prognosis patients undergoing assisted reproductive technology: POSEIDON criteria-the why. Front Endocrinol 2018; 9: 461.##The ESHRE Guideline Group on Ovarian Stimulation, Bosch E, Broer S, Griesinger G, Grynberg M, Humaidan P, et al. ESHRE guideline: Ovarian stimulation for IVF/ICSI. Hum Reprod Open 2020; 2020: 1-13.##Broer SL, van Disseldorp J, Broeze KA, Dolleman M, Opmeer BC, Bossuyt P, et al. Added value of ovarian reserve testing on patient characteristics in the prediction of ovarian response and ongoing pregnancy: An individual patient data approach. Hum Reprod Update 2013; 19: 26-36.##Dewailly D, Andersen CY, Balen A, Broekmans F, Dilaver N, Fanchin R, et al. The physiology and clinical utility of anti-Müllerian hormone in women. Hum Reprod Update 2014; 20: 370-385.##https://doi.org/10.1093/humupd/dmu043##La Marca A, Ferraretti AP, Palermo R, Ubaldi FM. The use of ovarian reserve markers in IVF clinical practice: A national consensus. Gynecol Endocrinol 2016; 32: 1-5.##Clemente Nd, Racine C, Pierre A, Taieb J. Anti-Mullerian hormone in female reproduction. Endocrine Rev 2021; 42: 753-782.##Racoubian E, Aimagambetova G, Finan RR, Almawi WY. Age-dependent changes in anti-Müllerian hormone levels in Lebanese females: Correlation with basal FSH and LH levels and LH/FSH ratio: A cross-sectional study. BMC Women's Health 2020; 20: 134.##Li R, Gong F, Zhu Y, Fang W, Yang J, Liu J, et al. Anti-Müllerian hormone for prediction of ovarian response in Chinese infertile women undergoing IVF/ICSI cycles: A prospective, multi-centre, observational study. Reprod Biomed Online 2016; 33: 506-512.##Iwase A, Osuka S, Goto M, Murase T, Nakamura T, Takikawa S, et al. Clinical application of serum anti-Müllerian hormone as an ovarian reserve marker: A review of recent studies. J Obstet Gynaecol Res 2018; 44: 998-1006.##Zebitay AG, Cetin O, Verit FF, Keskin S, Sakar MN, Karahuseyinoglu S, et al. The role of ovarian reserve markers in prediction of clinical pregnancy. J Obstet Gynaecol 2017; 37: 492-497.##Stracquadanio M, Ciotta L, Palumbo MA. Relationship between serum anti-Mullerian hormone and intrafollicular AMH levels in PCOS women. Gynecol Endocrinol 2018; 34: 223-228.##Wiweko B, Maidarti M, Priangga MD, Shafira N, Fernando D, Sumapraja K, et al. Anti-mullerian hormone as a diagnostic and prognostic tool for PCOS patients. J Assist Reprod Genet 2014; 31: 1311-1316.##Tal R, Seifer DB. Potential mechanisms for racial and ethnic differences in anti-Müllerian hormone and ovarian reserve. Int J Endocrinol 2013; 2013: 818912.##Elchuri SV, Patterson BC, Brown MR, Buchanan I, Mertens AC, Meacham LR. Anti-Mullerian hormone levels in American girls by age and race/ethnicity. J Pediatr Endocrinol Metab 2015; 28: 189-193.##Bedenk J, Vrtacnik-Bokal E, Virant-Klun I. The role of anti-Mullerian hormone (AMH) in ovarian disease and infertility. J Assist Reprod Genet 2020; 37: 89-100.##Schuh-Huerta SM, Johnson NA, Rosen MP, Sternfeld B, Cedars MI, Reijo Pera RA. Genetic variants and environmental factors associated with hormonal markers of ovarian reserve in Caucasian and African American women. Hum Reprod 2012; 27: 594-608.##Gleicher N, Weghofer A, Kim A, Barad DH. The impact in older women of ovarian FMR1 genotypes and sub-genotypes on ovarian reserve. PLoS One 2012; 7: e33638.##Schuh-Huerta SM, Johnson NA, Rosen MP, Sternfeld B, Cedars MI, Reijo Pera RA. Genetic markers of ovarian follicle number and menopause in women of multiple ethnicities. Hum Genet 2012; 131: 1709-1724.##Kushnir VA, Seifer DB, Barad DH, Sen A, Gleicher N. Potential therapeutic applications of human anti-Müllerian hormone (AMH) analogues in reproductive medicine. J Assist Reprod Genet 2017; 34: 1105-1113.##Kedem A, Haas J, Geva LL, Yerushalmi G, Gilboa Y, Kanety H, et al. Ongoing pregnancy rates in women with low and extremely low AMH levels. A multivariate analysis of 769 cycles. PLoS One 2013; 8: e81629.##Chinta P, Antonisamy B, Mangalaraj AM, Kunjummen AT, Kamath MS. POSEIDON classification and the proposed treatment options for groups 1 and 2: Time to revisit? A retrospective analysis of 1425 ART cycles. Hum Reprod Open 2021; 2021: hoaa070.##Adanaş Aydın G, Yavuz A, Terzi H, Kutlu T. Assessment of the relationship of basal serum anti-Mullerian hormone levels with oocyte quality and pregnancy outcomes in patients undergoing ICSI. Iran J Reprod Med 2015; 13: 231-236.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>


	<ARTICLE> 
		<TitleF>A successful twin healthy live birth achieved from eggs with a rare perivitelline space abnormality: A case report</TitleF>
		<TitleE>یک تولد زنده سالم و موفق دوقلو حاصل از تخمک های با ناهنجاری نادر فضای پری‌ویتلین: گزارش مورد</TitleE>
		<TitleLang_ID>2</TitleLang_ID>
		<ABSTRACTS>
			<ABSTRACT>
			<Language_ID>1</Language_ID>
			<CONTENT>مقدمه: مشاهده بدشکلی فنوتیپی در تخمک انسان به&#8204; ویژه در فضای پری&#8204;ویتلین گاهی اتفاق می&#173;افتد که از مهم&#8204;ترین انحرافات جزء اضافی سیتوپلاسمی است.
مورد: مورد زنی 30 ساله بدون بارداری قبلی بود که برای اولین بار اقدام به درمان لقاح آزمایشگاهی می&#173;کرد. با توجه به مقدار بسیار زیاد ذرات گرانولار موجود در فضای پری&#8204;ویتلین، که پس از عمل جداسازی قابل مشاهده بود، امکان تعیین حضور و موقعیت اولین جسم قطبی برای درک درست بلوغ تخمک وجود نداشت (متافاز 2). با این وجود، در تمام تخمک&#173;ها تزریق داخل سیتوپلاسمی اسپرم انجام شد. برای انجام کل مراحل کشت از دستگاه انکوباتور تایم لپس استفاده شد. از این رو، فیلم 6 روزه کشت ضبط شد. تنها 2 تخمک توانستند به درستی بارور شوند و در روز 6 به مرحله بلاستوسیست برسند. جنین&#173;ها منجمد شدند و متعاقباً به عنوان انتقال جنین منجمد پس از سیکل قاعدگی بعدی منتقل شدند.
نتیجه &#173;گیری: به نظر می&#8204;رسد وجود استثنایی ذرات گرانولار در فضای پری&#8204;ویتلین که جنبه&#8204;ها و رفتار سلول&#8204;های گرانولوزا را به ما یادآوری می&#8204;کند، بر لقاح تأثیر می&#8204;گذارد اما بر کیفیت بلاستوسیست تأثیر نمی&#8204;گذارد. در واقع این زن پس از انتقال جنین موفق به تولد دوقلو شد.</CONTENT>
			</ABSTRACT>
			<ABSTRACT>
			<Language_ID>2</Language_ID>
			<CONTENT>Background: Phenotypic dysmorphism is not rare to be found in the human oocyte, especially in the perivitelline space, which are among the most important aberration of the extra cytoplasmic component. 
Case Presentation: The case is of a 30-yr-old woman with no previous pregnancy, attempting an in vitro fertilization treatment for the first time. Given the extraordinary quantity of granular particles found in the perivitelline space, visible after the stripping procedure, it was not possible to establish the presence and position of the first polar body to appreciate the correct oocyte maturation (metaphase 2). Nevertheless, all the eggs were injected by the intracytoplasmic sperm injection. A time lapse incubator was used to perform the entire culture. Hence, a record of 6 days culture video was obtained. Only 2 eggs could fertilize correctly and reach the blastocyst stage on day 6. The embryos were frozen and subsequently transferred as frozen embryo transfer following the next menstrual cycle. 
Conclusion: The exceptional presence of granular particles in the perivitelline space, which reminds us for aspects and behavior the granulosa cells, seems to affected the fertilization but not the blastocysts quality. As a matter of fact the woman, after the embryo transfer, achieved a successful twin live birth.</CONTENT>
			</ABSTRACT>
		</ABSTRACTS>

		<PAGES>
			<PAGE>
			<FPAGE>263</FPAGE>
			<TPAGE>267</TPAGE>
			</PAGE>
		</PAGES>

		<RECEIVE_DATE>
			2022/07/252022/10/252022/08/312021/08/132021/08/192022/07/102021/11/112022/06/30
		</RECEIVE_DATE>

		<RECEIVE_DATE_FA>
			1401/4/9
		</RECEIVE_DATE_FA>

		<ACCEPT_DATE>
			2023/01/212023/01/212023/01/232023/02/12023/01/232023/02/142023/02/142023/01/15
		</ACCEPT_DATE>

		<ACCEPT_DATE_FA>
			1401/10/25
		</ACCEPT_DATE_FA>

		<AUTHORS>
			<AUTHOR>
				<Name>Daniele</Name>
				<MidName></MidName>
				<Family>Ferri</Family>
				<NameE>Daniele</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Ferri</FamilyE>
				<Organizations>
				<Organization>Momo Fertilife Clinic, Via Cala Dell’Arciprete 2C, Bisceglie, Italy.</Organization>
				</Organizations>
				<Countries>
				<Country>ایتالیا</Country>
				</Countries>
				<EMAILS>
				<Email>danieleferrimomo@gmail.com</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Domenico</Name>
				<MidName></MidName>
				<Family>Baldini</Family>
				<NameE>Domenico</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Baldini</FamilyE>
				<Organizations>
				<Organization>Momo Fertilife Clinic, Via Cala Dell’Arciprete 2C, Bisceglie, Italy.</Organization>
				</Organizations>
				<Countries>
				<Country>ایتالیا</Country>
				</Countries>
				<EMAILS>
				<Email>dbaldini@libero.it</Email>
				</EMAILS>
			</AUTHOR>

			<AUTHOR>
				<Name>Giorgio Maria</Name>
				<MidName></MidName>
				<Family>Baldini</Family>
				<NameE>Giorgio Maria</NameE>
				<MidNameE></MidNameE>
				<FamilyE>Baldini</FamilyE>
				<Organizations>
				<Organization>Momo Fertilife Clinic, Via Cala Dell’Arciprete 2C, Bisceglie, Italy.</Organization>
				</Organizations>
				<Countries>
				<Country>ایتالیا</Country>
				</Countries>
				<EMAILS>
				<Email>gbaldini97@gmail.com</Email>
				</EMAILS>
			</AUTHOR>
		</AUTHORS>


		<KEYWORDS>
			<KEYWORD>
				<KeyText>Oocyte</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Granulosa cell</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Intracytoplasmic sperm injection</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Perivitelline space</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>Case report.</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>تخمک</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>سلول گرانولوزا</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>تزریق داخل سیتوپلاسمی اسپرم</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>فضای پریویتلین</KeyText>
			</KEYWORD>

			<KEYWORD>
				<KeyText>گزارش مورد.</KeyText>
			</KEYWORD>
		</KEYWORDS>

		<REFRENCES>
			<REFRENCE>
				<REF>Sousa M, Teixeira da Silva J, Silva J, Cunha M, Viana P, Oliveira E, et al. Embryological, clinical and ultrastructural study of human oocytes presenting indented zona pellucida. Zygote 2015; 23: 145-157.##Nikiforov D, Grøndahl ML, Hreinsson J, Andersen CY. Human oocyte morphology and outcomes of infertility treatment: A systematic review. Reprod Sci 2022; 29: 2768-2785.##Jansen R, Mortimer D. Toward reproductive certainty: Fertility and genetics beyond, the plenary proceedings of the 10th world congress. London: CRC Press; 1999.##Gupta SK. The human egg's zona pellucida. Curr Top Dev Biol 2018; 130: 379-411.##Turathum B, Gao EM, Chian RC. The function of cumulus cells in oocyte growth and maturation and in subsequent ovulation and fertilization. Cells 2021; 10: 2292.## ##</REF>
			</REFRENCE>
		</REFRENCES>

	</ARTICLE>

</ARTICLES>

</JOURNAL>
</XML>
