the frequency of yq microdeletion in azoospermic and oligospermic iranian infertile men

نویسندگان

mohammad ali zaimy

seyyed mehdi kalantar

mohammad hasan sheikhha

tahere jahaninejad

چکیده

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.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

The frequency of Yq microdeletion in azoospermic and oligospermic Iranian infertile men

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 ...

متن کامل

Frequency of Y Chromosome Microdeletions in Azoospermic and Oligospermic Iranian Infertile Men

Background and Aims: Azoospermia factor (AZF) region of the Y-chromosome has several genes which are responsible for normal spermatogenesis. Microdeletions of these genes are associated with azoospermia and oligospermia. These microdeletions are too small to be detected by karyotyping. They can be easily identified using polymerase chain reaction. The aim of this study is to determine the frequ...

متن کامل

chromosomal anomalies in infertile azoospermic and oligospermic men

in this study, chromosome analyses were performed on 70 infertile azoospermic and oligospermic (<20 million/ml) men, and also cultures of peripheral blood lymphocytes by high resolution banding method were analysed as well. it is revealed 8 (11.43 percent) men with chromosomal abnormality. there were 31.4 percent patients with azoospermia and 68.6 percent with oligospermia from several thousand...

متن کامل

P-236: Haplotype Analysis of The H2B.W Gene in Severe Oligospermic and Azoospermic Infertile Men Referred to Royan Institute

Background: Recent studies demonstrated the multifactorial and chronic nature of male infertility, including mutations of some known spermatogenesis-related genes. The H2B family, member W (H2B.W) gene is one of the testis specific histone variant genes that encodes a sperm telomere-binding protein, required for reorganization and integration of sperm chromosomes. The objective of the present s...

متن کامل

P-208: Analysis of H2BFWT Gene Alterations in Severe Oligospermic and Azoospermic Infertile Men Referred to Royan Institute

Background: Telomeres play a dramatic role in sperm pronuclei formation and subsequently successful fertilization. The H2B family, member W, testis specific (H2BFWT) gene encodes a testis specific histone that colocalized with telomeric sequences and interfere in the dynamic rearrangement of telomeres at late stages of spermatogenesis. H2BFWT is essential for transmission of the telomeric chrom...

متن کامل

The prevalence of Human Papilloma Virus (HPV) infection in the oligospermic and azoospermic men

Background: Human papilloma virus (HPV) infection is one of the most common sexually transmitted diseases that affects men like women and infected cutaneous and mucosal squamous epithelium. The aim of the present study was to determine the prevalence of HPV in the semen of oligospermic, azoospermic and normal patients. Methods: From June 2012 to June 2013, a total of 90 individuals were enro...

متن کامل

منابع من

با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید


عنوان ژورنال:
international journal of reproductive biomedicine

جلد ۱۱، شماره ۶، صفحات ۴۵۳-۰

میزبانی شده توسط پلتفرم ابری doprax.com

copyright © 2015-2023