Volume 11, Issue 6 (9-2013)                   IJRM 2013, 11(6): 453-0 | Back to browse issues page

XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Zaimy M A, Kalantar S M, Sheikhha M H, Jahaninejad T, Pashaiefar H, Ghasemzadeh J et al . The frequency of Yq microdeletion in azoospermic and oligospermic Iranian infertile men. IJRM 2013; 11 (6) :453-0
URL: http://ijrm.ir/article-1-428-en.html
1- Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
2- Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences, Yazd, Iran , smkalantar@yahoo.com
3- Department of Genetics, Faculty of Medical Sciences, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
Abstract:   (2904 Views)
Background: About 15% of couples have infertility problems which 40% of them are related to the male factors. Genetic factors are candidate for about 10% of male infertility conditions. Among these, AZFa, AZFb, AZFc and AZFd regions on the Yq are considered most important for spermatogenesis. Microdeletions of these regions are thought to be involved in some cases of azoospermic or oligospermic infertile men.
Objective: We studied the prevalence of AZF microdeletions among Iranian infertile men with non-obstructive azoospermia and oligospermia.
Materials and Methods: A total of 50 Iranian azoospermic and oligospermic infertile men were selected for case group and 50 men with normal spermogram as control group. The molecular study of Y chromosome microdeletions was done by multiplex polymerase chain reaction (M-PCR) method by using of 13 sequence tagged site (STS) markers from AZF region.
Results: Four (8%) patients showed Y chromosome microdeletions among case group, deletion in AZFc region was the most frequent (80%) followed by AZFb (20%), in AZFa and AZFd region we did not detect any deletions. No deletion was detected in control group; the ratio of Y chromosome microdeletion in azoospermic men was higher than this ratio in oligospermic men [19% (3/16) among azoospermic men and 3% (1/34) among oligospermics]. Serum FSH level in men with microdeletions was higher than this level in men with no deletions (p=0.034).
Conclusion: Because of relatively high prevalence of microdeletions on the long arm of Y chromosome among Iranian azoospermic and oligospermic patients, screening of this microdeletion may be advised to infertile men particularly azoospermic and oligospermic men before using assisted reproductive treatments.
Full-Text [PDF 284 kb]   (509 Downloads) |   |   Full-Text (HTML)  (591 Views)  
Type of Study: Original Article |

References
1. Balkan M, Tekes S, Gedik A. Cytogenetic and Y chromosome microdeletion screening studies in infertile males with oligozoospermia and azoospermia in southeast Turkey. J Assist Reprod Genet 2008; 25: 559-565. [DOI:10.1007/s10815-008-9272-8]
2. Nagvenkar P, Desai K, Hinduja I, Zaveri K. Chromosomal studies in infertile men with oligozoospermia & non-obstructive azoospermia. Indian J Med Res 2005; 122: 34-42.
3. Dada R, Gupta NP, Kucheria K. Molecular screening for Yq microdeletion in men with idiopathic oligozoospermia and azoospermia. J Bioscie 2003; 28: 163-168. [DOI:10.1007/BF02706215]
4. Skakkebaek NE, Giwercman A, de Kretser D. Pathogenesis and management of male infertility. Lancet 1994; 343: 1473-1479. [DOI:10.1016/S0140-6736(94)92586-0]
5. Vutyavanich T, Piromlertamorn W, Sirirungsi W, Sirisukkasem S. Frequency of Y chromosome microdeletions and chromosomal abnormalities in infertile Thai men with oligozoospermia and azoospermia. Asian J Androl 2007; 9: 68-75. [DOI:10.1111/j.1745-7262.2007.00239.x]
6. Krausz C, Quintana-Murci L, McElreavey K. Prognostic value of Y deletion analysis: what is the clinical prognostic value of Y chromosome microdeletion analysis? Hum Reprod 2000; 15: 1431-1444. [DOI:10.1093/humrep/15.7.1431]
7. Kleiman SE, Yogev L, Gamzu R, Hauser R, Botchan A, Lessing JB, et al. Genetic evaluation of infertile men. Hum Reprod 1999; 14: 33-38. [DOI:10.1093/humrep/14.1.33]
8. Behulova R, Varga I, Strhakova L, Bozikova A, Gabrikova D, Boronova I, et al. Incidence of microdeletions in the AZF region of the Y chromosome in Slovak patients with azoospermia. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 2011; 155: 33-38. [DOI:10.5507/bp.2011.006]
9. Vergnaud G, Page DC, Simmler MC, Brown L, Rouyer F, Noel B, et al. A deletion map of the hyman Y chromosome based on DNA hybridization. Am J Hum Genet 1986; 38 109-124.
10. Kent-First M, Muallem A, Shultz J, Pryor J, Roberts K, Nolten W, et al. Defining regions of the Y-chromosome responsible for male infertility and identification of a fourth AZF region (AZFd) by Y-chromosome microdeletion detection. Mol Reprod Dev 1999; 53: 27-41. https://doi.org/10.1002/(SICI)1098-2795(199905)53:1<27::AID-MRD4>3.0.CO;2-W [DOI:10.1002/(SICI)1098-2795(199905)53:13.0.CO;2-W]
11. Sadeghi-Nejad H, Farrokhi F. Genetics of azoospermia: Current knowledge, clinical implications, and future directions. Urol J 2007; 4: 192-206.
12. Raicu F, Popa L, Apostol P, Cimponeriu D, Dan L, Ilinca E, et al. Screening for microdeletions in human Y chromosome-AZF candidate genes and male infertility. J Cell Mol Med 2003; 7: 43-48. [DOI:10.1111/j.1582-4934.2003.tb00201.x]
13. Page DC, Silber S, Brown LG. Men with infertility caused by AZFc deletion can produce sons by intracytoplasmic sperminjection, but are likely to transmit the deletion and infertility. Hum Reprod 1999; 14: 1722-1726. [DOI:10.1093/humrep/14.7.1722]
14. Kuhnert B, Gromoll J, KostovaE, Tschanter P, Luetjens CM, SimoniM, et al. Case report: natural transmission of an AZFc Y-chromosomal microdeletion from father to his sons. Hum Reprod 2004; 19: 886-888. [DOI:10.1093/humrep/deh186]
15. Kamischke A, Gromoll J, Simoni M, Behre HM, Nieschlag E. Transmission of a Y chromosomal deletion involving the deleted in azoospermia (DAZ) and chromodomain (CDY1) genes from father to son through intracytoplasmic sperminjection: case report. Hum Reprod 1999; 14 : 2320-2322. [DOI:10.1093/humrep/14.9.2320]
16. Malekasgar AM, Mombaini H. Screening of 'Y' chromosome microdeletions in Iranian infertile males. J Hum Reprod Sci 2008; 1: 2-9. [DOI:10.4103/0974-1208.38973]
17. Mirfakhraie R, Mirzajani F, Kalantar SM, Montazeri M, Salsabili N, Pourmand GR, et al. High prevalence of AZFb microdeletion in Iranian patients with idiopathic non-obstructive azoospermia. Indian J Med Res 2010; 132: 265-270.
18. Simoni M, Bakker E, Krausz C. EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004. Int J Androl 2004; 27: 240-249. [DOI:10.1111/j.1365-2605.2004.00495.x]
19. Poongothai J, Gopenath TS, Manonayaki S. Genetics of human male infertility. Singapore Med J 2009; 50: 336-347.
20. Omrani MD, Samadzadae S, Bagheri M, Attar K. Y Chromosome microdeletions in idiopathic infertile menfrom West Azarbaijan. Urol J 2006; 3: 38-43.
21. Silber SJ, Alagappan R, Brown LG, Page DC. Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplasmic sperm injection after testicular sperm extraction. Hum Reprod 1998; 13: 3332-3337. [DOI:10.1093/humrep/13.12.3332]
22. Miller SA, Dykes DD. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988; 16: 1215. [DOI:10.1093/nar/16.3.1215]

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Designed & Developed by : Yektaweb