DAZL A386G gene mutation and male infertility: A genetic association analysis of Asian population
نویسندگان
چکیده
Genetic susceptibility has a prominent role in infertility. This study was proposed the association of Deleted in Azoospermia-Like (DAZL) A386G gene transition with male infertility in an Iranian population which followed by a meta-analysis in Asian population. In the case-control study we collected blood samples from 100 idiopathic infertile and 100 healthy fertile men. After DNA extraction, DAZL A386G genotyping was performed by PCR-RFLP method. In meta-analysis, we found eligible papers by searching in standard databases. Case-control study indicated that there is no signifi cant association between DAZL A386G and male infertility in study population. However in metaanalysis, we found a signifi cant association between DAZL A386G and male infertility in G vs. A (OR= 8.33, 95% CI= 3.56-19.46, P < 0.001), AG vs. AA (OR= 7.60, 95% CI= 3.24-17.82, P < 0.001), and AG+GG vs. AA (OR= 8.13, 95% CI= 3.47-19.07, P < 0.001) genetic models within Asian population. Therefore, we concluded that DAZL A386G can be considered as a possible risk factor for susceptibility to male infertility within Asian population. However, further studies with larger sample sizes are required to obtain more accurate data.
منابع مشابه
A386G transition in DAZL gene is not associated with spermatogenic failure in Tamil Nadu, South India
The DAZ-like (DAZL) gene located on the short arm of autosomal chromosome 3 (3p24), an essential master gene for the premeiotic development of male and female germ cells, is the father of the Y-chromosome DAZ gene cluster and encodes for RNA-binding proteins. Reported instances of positive association of DAZL gene mutations with infertility in men have been found in a Taiwanese population but n...
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