Laboratory of Genetics, Comparative and Evolutionary Biology, Department of Biochemistry and Biotechnology, University of Thessaly, Larisa, Greece.
Embryolab IVF Unit, Thessaloniki, Greece.
Mol Biol Rep. 2021 May;48(5):4967-4972. doi: 10.1007/s11033-021-06470-2. Epub 2021 Jun 7.
Genome-wide association studies have paved the way for the discovery of new markers regarding many diseases, including male infertility. A previous study on Caucasians highlighted 172 polymorphisms for their putative association with male infertility and we attempted to replicate these findings on our dataset comprising of Greek male individuals (n = 360). We retrieved 59 out of 172 polymorphisms and tested for all association models on 278 normospermic men and 82 patients with an abnormal seminogram, later separated into oligozoospermic and asthenozoospermic groups. Our findings indicate that two SNPs (rs2296225 in KIF17, rs7224496 in SMYD4) are associated with male infertility in the Greek population and have not been recorded in literature as of yet. These novel markers need further validation via additional studies and an increased individual number. All in all, replication studies, possess the power to validate existing polymorphisms found across all population and thus increase both statistical significance as well as identify novel potentially diagnostic markers.
全基因组关联研究为发现许多疾病(包括男性不育症)的新标志物铺平了道路。之前针对白种人的一项研究强调了 172 种多态性,认为它们与男性不育症有关,我们试图在包括希腊男性个体(n=360)的数据集上复制这些发现。我们从 172 种多态性中检索到 59 种,并在 278 名正常精子症男性和 82 名精液分析异常的患者(进一步分为少精子症和弱精子症组)中测试了所有关联模型。我们的研究结果表明,在希腊人群中,两个 SNP(rs2296225 在 KIF17 中,rs7224496 在 SMYD4 中)与男性不育症相关,并且尚未在文献中记录。这些新的标志物需要通过更多的研究和增加个体数量来进一步验证。总之,复制研究具有验证所有人群中发现的现有多态性的能力,从而提高统计显著性并确定新的潜在诊断标志物。