Meng J, Mu X, Wang Y M
School of Medicine, Yanan University, Yanan, Luochuan, China.
Genet Mol Res. 2013 Jun 11;12(2):1808-15. doi: 10.4238/2013.June.11.1.
Polymorphisms of estrogen receptor (ER) genes have been implicated in male infertility, but studies of this association have produced conflicting results. The present study was conducted to examine whether polymorphisms within the ERα and ERβ genes are susceptibility factors for human male idiopathic infertility in Chinese men. We investigated the association between the ERα gene gene and PvuII and XbaI polymorphisms and the ERβ gene and RsaI and AluI polymorphisms and idiopathic male infertility in Han Chinese men. A total of 204 men with oligozoospermia (sperm count <20 x 10(6)/mL) or azoospermia and 252 fertile control men were included in this study. The analysis revealed a strong association between the XbaI genotype distribution and impaired spermatogenesis (P = 0.0018). The frequency of the G allele was significantly lower in patients than in controls (P = 0.003). Furthermore, serum levels of follicle-stimulating hormone and luteinizing hormone in XbaI AA carriers were significantly higher than those in AG or GG carriers. Our findings further support a possible role of ERα in male infertility. Further studies are needed to replicate our findings, as well as to elucidate more fully the biological mechanisms of the modulation of ERα on human spermatogenesis.
雌激素受体(ER)基因多态性与男性不育有关,但关于这种关联的研究结果相互矛盾。本研究旨在探讨ERα和ERβ基因内的多态性是否是中国男性特发性不育的易感因素。我们调查了汉族男性中ERα基因的PvuII和XbaI多态性、ERβ基因的RsaI和AluI多态性与特发性男性不育之间的关联。本研究共纳入204名少精子症(精子计数<20×10⁶/mL)或无精子症男性以及252名生育力正常的对照男性。分析显示XbaI基因型分布与精子发生受损之间存在强关联(P = 0.0018)。患者中G等位基因的频率显著低于对照组(P = 0.003)。此外,XbaI AA携带者的血清促卵泡生成素和黄体生成素水平显著高于AG或GG携带者。我们的研究结果进一步支持了ERα在男性不育中可能发挥的作用。需要进一步的研究来重复我们的发现,并更全面地阐明ERα对人类精子发生调节的生物学机制。