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Association of polymorphisms in glutathione S-transferase genes (GSTM1 GSTT1 GSTP1) with idiopathic azoospermia or oligospermia in Sichuan China

机译:谷胱甘肽S-转移酶基因(GSTM1GSTT1GSTP1)多态性与四川特发性无精症或少精症的关系

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摘要

The reported effects of the glutathione S-transferase (GSTs) genes (GSTM1, GSTT1, and GSTP1) on male factor infertility have been inconsistent and even contradictory. Here, we conducted a case-control study to investigate the association between functionally important polymorphisms in GST genes and idiopathic male infertility. The study group consisted of 361 men with idiopathic azoospermia, 118 men with idiopathic oligospermia, and 234 age-matched healthy fertile male controls. Genomic DNA was extracted from the peripheral blood, and analyzed by polymerase chain reaction and restriction fragment length polymorphism analysis. There was a significant association between the GSTP1 variant genotype (Ile/Val + Val/Val) with idiopathic infertility risk (odds ratio [OR]: 1.53; 95% confidence interval [CI]: 1.11–2.11; P = 0.009). Similarly, a higher risk of infertility was noted in individuals carrying a genotype combination of GSTT1-null and GSTP1 (Ile/Val + Val/Val) (OR: 2.17; 95% CI: 1.43–3.31; P = 0.0002). These results suggest an increased risk of the GSTP1 variant genotype (Ile/Val + Val/Val) for developing male factor infertility. Our findings also underrate the significance of the effect of GSTM1 and/or GSTT1 (especially the former) in modulating the risk of male infertility in males from Sichuan, southwest China.
机译:谷胱甘肽S-转移酶(GSTs)基因(GSTM1,GSTT1和GSTP1)对男性不育症的报道影响不一致,甚至矛盾。在这里,我们进行了一项病例对照研究,以研究GST基因中功能重要的多态性与特发性男性不育症之间的关系。该研究组由361名特发性无精症男性,118名特发性少精症男性和234个与年龄匹配的健康可育男性对照组组成。从外周血中提取基因组DNA,并通过聚合酶链反应和限制性片段长度多态性分析进行分析。 GSTP1变异基因型(Ile / Val + Val / Val)与特发性不孕风险之间存在显着相关性(几率[OR]:1.53; 95%置信区间[CI]:1.11-2.11; P = 0.009)。同样,携带GSTT1-null和GSTP1基因型组合的个体(Ile / Val + Val / Val)的不孕风险更高(OR:2.17; 95%CI:1.43-3.31; P = 0.0002)。这些结果表明,GSTP1变异基因型(Ile / Val + Val / Val)发生男性不育症的风险增加。我们的发现还低估了GSTM1和/或GSTT1(特别是前者)在调节中国西南地区四川省男性不育风险中的意义。

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