<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>International Journal of Reproductive BioMedicine</title>
<title_fa>International Journal of Reproductive BioMedicine</title_fa>
<short_title>IJRM</short_title>
<subject>Medical Sciences</subject>
<web_url>http://ijrm.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2476-4108</journal_id_issn>
<journal_id_issn_online>2476-3772</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.29252/ijrm</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1397</year>
	<month>11</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2019</year>
	<month>2</month>
	<day>1</day>
</pubdate>
<volume>17</volume>
<number>2</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Evaluation of the metformin effects on Anti-Müllerian Hormone in women with polycystic ovarian syndrome: A double-blind randomized clinical trial</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa>Letter to Editor</content_type_fa>
	<content_type>Letter to Editor</content_type>
	<abstract_fa></abstract_fa>
	<abstract>Anti-M&amp;uuml;llerian hormone (AMH) is made by the granulosa cells of preantral and small&amp;nbsp;antral follicles which blocks the transition from the primordial to the primary follicular&amp;nbsp;stage. Metformin may be associated with a decrease in AMH serum level and antral&amp;nbsp;follicles in women who suffer from polycystic ovary syndrome (PCOs)&lt;br&gt;
It was reported that metformin in women with polycystic ovary syndrome (PCOs) is&amp;nbsp;associated with a decrease in both AMH serum level and antral follicles.&lt;br&gt;
The objective of the current letter was the evaluation of the effects of metformin&amp;nbsp;on hormonal profile of women with PCOs. In this prospective, randomized, doubleblind&amp;nbsp;controlled clinical trial, 42 women (aged 17&amp;ndash;45 yr) with PCOs who were randomly&amp;nbsp;allocated to receive 500 mg Metformin orally three times a day or placebo for&amp;nbsp;three months were included. Fasting plasma glucose, follicular stimulating hormone,&amp;nbsp;luteinizing hormone (LH), prolactin (PRL), testosterone and AMH levels were measured&amp;nbsp;at baseline and at the end of the period. In this study, independent and paired t-test&amp;nbsp;were used for quantitative comparison and chi-square analysis for qualitative variables.&amp;nbsp;Logistic regression analysis was done to identify independent risk factors, and Pvalue&amp;nbsp;of lower than 0.05 were considered significant. All of the statistical analyses&amp;nbsp;were done by SPSS software, version 20.0. We didn&amp;rsquo;t find any significant change&amp;nbsp;after the study between treatment and control groups in hormonal profiles especially&amp;nbsp;AMH. However, in subgroup analysis, we revealed that AMH and LH levels decreased&amp;nbsp;significantly in normal weight patients (p= 0.024, 0.048, respectively) and prolactin&amp;nbsp;levels in subgroup of overweight patients (p= 0.001). Moreover, patients in metformin&amp;nbsp;group at the end of study had more regular menses, more weight loss, and lower&amp;nbsp;hair loss (p= .001, 0.04, 0.014, respectively). Women with PCOs have elevated levels&amp;nbsp;of LH that is secondary to increased sensitivity of pituitary to GnRH. Increased levels&lt;br&gt;
of LH lead to hyperandrogenism. Metformin can improve this condition. In this study,&amp;nbsp;we observed that LH was decreased significantly in the metformin group of PCOs&amp;nbsp;patients (p= 0.05). It is in agreement with some of the previous studies, however, De&amp;nbsp;Leo and et al. reported a non-significant decrease in LH levels after treatment with&amp;nbsp;metformin (1). Pieces of evidence showed that AMH levels in PCOs patients are 2 to 3&amp;nbsp;times higher than age-matched normal women (2), and this condition is a marker for&amp;nbsp;PCOs and can be a surrogate test of hyperandrogenism (3). Metformin in our study&amp;nbsp;improved the irregularity in the menstrual cycle (p&lt; 0.001), hair loss (p= 0.014), and&amp;nbsp;prolactin secretion (p= 0.024), as well as LH secretion (p= 0.05); however, it didn&amp;rsquo;t&amp;nbsp;show any significant decrease on AMH levels. Metformin can reduce ovarian volume&amp;nbsp;in PCOs patients especially in hyperinsulinemic subgroups (4); however, we observed&amp;nbsp;that in normal weight subgroup of patients, metformin decreased AMH significantly&amp;nbsp;(p= 0.024), and in overweight or obese patients, prolactin decreased in response&amp;nbsp;to metformin, significantly (p= 0.001). Moreover, metformin leads to improvement in&amp;nbsp;follicular development with fewer percentage of preantral follicles and cysts and higher&amp;nbsp;percentages of antral follicles (5). Considering these pieces of evidence, it seems that&amp;nbsp;AMH after metformin treatment in PCOs patients was secret in comparable amounts of&amp;nbsp;pretreatment; however, the source of secretion after starting metformin is different from&amp;nbsp;pretreatment and switched from small follicles and cysts to more developed follicles&amp;nbsp;and structures such as antral follicles and corpora lutea. Further investigations that can&amp;nbsp;differentiate secreted AMH from a different source will shed more light on this field.&amp;nbsp;The most important limitation of our study is the small sample size. GI side effects of&amp;nbsp;metformin caused some patients in metformin group to refuse getting the treatment.&amp;nbsp;Studies with more attendants can display the difference between different phenotypes&amp;nbsp;of PCOs patients in response to metformin. In conclusion, this study showed that&lt;br&gt;
metformin can cause favorable effects on the hormonal profile of PCOs patients, and&amp;nbsp;although AMH levels were not decreased significantly, menstruation improved in the&amp;nbsp;treated group.&lt;br&gt;
The most important limitation of our study is the small sample size. GI side effects of&amp;nbsp;metformin caused some patients in metformin group to refuse getting the treatment.&amp;nbsp;Studies with more attendants can display the difference between different phenotypes&amp;nbsp;of PCOs patients in response to metformin. In conclusion, this study showed that&amp;nbsp;metformin can cause favorable effects on the hormonal profile of PCOs patients, and&amp;nbsp;although AMH levels were not decreased significantly, menstruation improved in the&amp;nbsp;treated group.&lt;br&gt;
&amp;nbsp;</abstract>
	<keyword_fa></keyword_fa>
	<keyword></keyword>
	<start_page>143</start_page>
	<end_page>144</end_page>
	<web_url>http://ijrm.ir/browse.php?a_code=A-10-549-180&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Jam </first_name>
	<middle_name></middle_name>
	<last_name>Ashkezari</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>rahmanian@ssu.ac.ir</email>
	<code></code>
	<orcid>0000-0003-3851-6937</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Diabetes Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Nasim</first_name>
	<middle_name></middle_name>
	<last_name>Namiranian</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>rahmanian@ssu.ac.ir</email>
	<code></code>
	<orcid>0000-0002-5133-6204</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Diabetes Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Somaye </first_name>
	<middle_name></middle_name>
	<last_name>Gholami</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>rahmanian@ssu.ac.ir</email>
	<code></code>
	<orcid>0000-0002-1429-6688</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Diabetes Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Maryam</first_name>
	<middle_name></middle_name>
	<last_name>Elahi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>rahmanian@ssu.ac.ir</email>
	<code></code>
	<orcid>0000-0002-1440-0772</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Diabetes Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Masoud</first_name>
	<middle_name></middle_name>
	<last_name>Rahmanian</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>rahmanian@ssu.ac.ir</email>
	<code></code>
	<orcid>0000-0001-7601-7413</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Diabetes Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
