Singh Kiran, Raman Rajiva
Department of Molecular and Human Genetics, Banaras Hindu University, Varanasi, India.
Indian J Hum Genet. 2009 Jan;15(1):19-22. doi: 10.4103/0971-6866.50865.
Infertility being a multifactorial disorder, both genetic and environmental factors contribute to the etiology of infertile phenotype. Chromosomal anomalies and Y-microdeletion are the established genetic risk factors of male infertility. Y-haplotypes has been found as risk factor for male infertility in certain populations, though in certain others no association has been reported, suggesting a population-specific association of these variations with male infertility. In a case-control study, 165 azoo-/oligospermic patients and 200 controls were haplotyped for certain Y-haplogroups for a possible association with idiopathic male infertility in an Indian population. Analysed Y-haplogroups showed no association with infertile phenotype. Thus this genetic factor is not a risk for infertility in the studied Indian population but that does not rule out the possibility of any of them, to be a risk in other populations.
不孕症是一种多因素疾病,遗传和环境因素均对不育表型的病因有影响。染色体异常和Y染色体微缺失是公认的男性不育遗传风险因素。Y单倍型在某些人群中已被发现是男性不育的风险因素,不过在其他一些人群中未报告有相关性,这表明这些变异与男性不育存在人群特异性关联。在一项病例对照研究中,对165例无精子症/少精子症患者和200例对照进行了某些Y单倍群的单倍型分型,以探讨其与印度人群特发性男性不育的可能关联。分析的Y单倍群与不育表型无关联。因此,在该研究的印度人群中,这种遗传因素不是不育的风险因素,但这并不排除它们中的任何一个在其他人群中成为风险因素的可能性。