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首页> 外文期刊>Free Radical Biology and Medicine: The Official Journal of the Oxygen Society >Genetic variants in antioxidant genes are associated with sperm DNA damage and risk of male infertility in a Chinese population
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Genetic variants in antioxidant genes are associated with sperm DNA damage and risk of male infertility in a Chinese population

机译:抗氧化剂基因的遗传变异与中国人口的精子DNA损伤和男性不育风险相关

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摘要

To test the hypothesis that polymorphisms in antioxidant genes are more susceptible to sperm DNA damage and male infertility, we examined 11 single-nucleotide polymorphisms from six antioxidant genes (GPX1, CAT, PON1, NQO1, SOD2/MnSOD, and SOD3) in 580 infertility cases and 580 controls from a Chinese population-based case-control study (NJMU Infertility Study). Genotypes were determined using the OpenArray platform. Sperm DNA fragmentation was detected using the Tdt-mediated dUTP nick-end labeling assay, and the level of 8-hydroxydeoxyguanosine (8-OHdG) in sperm DNA was measured using immunofluorescence. The adjusted odds ratio and 95% confidence interval (CI) were estimated using unconditional logistic regression. The results indicated that the PON1 Arg192Glu (rs662) and SOD2 Val16Ala (rs4880) variant genotypes were associated with a significantly higher risk of male infertility. In addition, subjects carrying variant genotypes of both loci had a twofold (95% CI, 1.42-2.90) increase in the risk of male infertility, indicating a significant gene-gene interaction between these two loci (P for multiplicative interaction = 0.045). Moreover, linear regression analysis showed that individuals carrying the PON1 Arg192Glu (rs662) or SOD2 Val16Ala (rs4880) variants have significantly higher levels of sperm DNA fragmentation and 8-OHdG. These data suggest that genetic variations in antioxidant genes may contribute to oxidative sperm DNA damage and male infertility.
机译:为了检验抗氧化剂基因的多态性更易受精子DNA损伤和男性不育的假说,我们在580个不育症中检查了来自六个抗氧化剂基因(GPX1,CAT,PON1,NQO1,SOD2 / MnSOD和SOD3)的11个单核苷酸多态性一项基于中国人群的病例对照研究(NJMU不孕研究)得出的这些病例和580名对照。使用OpenArray平台确定基因型。使用Tdt介导的dUTP缺口末端标记检测法检测精子DNA片段化,并使用免疫荧光法检测精子DNA中的8-羟基脱氧鸟苷(8-OHdG)水平。使用无条件逻辑回归估计调整后的优势比和95%置信区间(CI)。结果表明,PON1 Arg192Glu(rs662)和SOD2 Val16Ala(rs4880)基因型与男性不育风险显着相关。此外,携带两个基因座变异基因型的受试者的男性不育风险增加了两倍(95%CI,1.42-2.90),表明这两个基因座之间存在显着的基因-基因相互作用(乘性相互作用的P = 0.045)。此外,线性回归分析显示,携带PON1 Arg192Glu(rs662)或SOD2 Val16Ala(rs4880)变异体的个体的精子DNA片段化水平和8-OHdG明显更高。这些数据表明抗氧化剂基因的遗传变异可能有助于氧化精子DNA损伤和男性不育。

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