Chihara Makoto, Yoshihara Kosuke, Ishiguro Tatsuya, Yokota Yuki, Adachi Sosuke, Okada Hiroyuki, Kashima Katsunori, Sato Takaaki, Tanaka Atsushi, Tanaka Kenichi, Enomoto Takayuki
Department of Obstetrics and Gynecology, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata, 951-8510, Japan.
J Assist Reprod Genet. 2015 Jun;32(6):903-8. doi: 10.1007/s10815-015-0468-4. Epub 2015 Apr 7.
A previous genome-wide association study in European men identified four single nucleotide polymorphism (SNP) loci associated with male infertility. Our aim was to replicate, if possible, the association of these SNPs with Japanese male infertility.
We genotyped four SNPs (rs5911500, rs10246939, rs2059807, and rs11204546) in 517 Japanese patients with male infertility and 369 fertile controls using SNP-specific real-time polymerase chain reaction TaqMan assays. Subsequently, we divided patients with male infertility into azoospermia (n = 417) and oligospermia subgroups (n = 70).
The four SNPs previously identified in European men showed no significant association with collective male infertility in our Japanese cohort. However, allele frequency analysis did indicate a significantly higher frequency of the rs11204546 C allele of the OR2W3 gene in the oligospermia subset of infertility patients compared with controls (p = 0.0037; odds ratio = 1.74; 95 % confidence interval, 1.21-2.53).
Although this study was somewhat limited by overall sample size, the OR2W3 gene polymorphism rs11204546 was significantly associated with oligospermia in Japanese men, suggesting that OR2W3 might be involved in genetic susceptibility to Japanese male infertility as well as in European males.
先前一项针对欧洲男性的全基因组关联研究确定了四个与男性不育相关的单核苷酸多态性(SNP)位点。我们的目的是尽可能复制这些SNP与日本男性不育的关联。
我们使用SNP特异性实时聚合酶链反应TaqMan分析法,对517名日本男性不育患者和369名生育能力正常的对照者进行了四个SNP(rs5911500、rs10246939、rs2059807和rs11204546)的基因分型。随后,我们将男性不育患者分为无精子症组(n = 417)和少精子症亚组(n = 70)。
先前在欧洲男性中鉴定出的这四个SNP在我们的日本队列中与男性不育总体上无显著关联。然而,等位基因频率分析确实表明,与对照组相比,不育患者少精子症亚组中OR2W3基因的rs11204546 C等位基因频率显著更高(p = 0.0037;优势比 = 1.74;95%置信区间,1.21 - 2.53)。
尽管本研究在总体样本量方面存在一定局限性,但OR2W3基因多态性rs11204546与日本男性的少精子症显著相关,这表明OR2W3可能与日本男性以及欧洲男性不育的遗传易感性有关。