Department of Medical Laboratory Sciences-IUG, Gaza, Palestine.
Biochem Genet. 2024 Dec;62(6):4303-4316. doi: 10.1007/s10528-023-10559-7. Epub 2024 Jan 31.
Semen possesses a variety of antioxidant defense mechanisms which protect sperm DNA from the damaging effects of oxidative stress. Correlation between antioxidant genes variants and sperm DNA fragmentation (SDF) level is not sufficiently studied. Therefore, we investigated the association between several single nucleotide polymorphisms (SNPs): CYP1A1 (rs1048943A > G), CYP4F2 (rs2108622G > A), NRF2 (rs6721961C > A), PON1 (rs662A > G), NOS3 (rs1799983G > T), GSTM1 (null), CAT (rs1001179C > T), SOD2 (rs4880A > G), GSTP1 (rs1695A > G), PON2 (rs7493G > C), EPHX2 (rs1042064T > C), and AHR (rs2066853G > A) and elevated SDF. The study employed a case-control design where, the allele and genotype frequencies of the selected SNPs were compared between 75 semen samples with abnormal SDF (the cases) and 75 samples with normal SDF (the controls). DNA was extracted from the semen samples and allele-specific PCR (AS-PCR) was used for genotyping the SNPs. Relevant data were collected from the patients' records et al.-Basma Fertility Center. Suitable statistical tests and multifactorial dimensionality reduction (MDR) test were used to anticipate SNP-SNP interactions. Comparison of semen parameters revealed significant differences between cases and controls in terms of liquefaction time, sperm total motility, and normal form. Genotype frequencies of NOS3 G > T (GT), SOD2 A > G (AA and AG), EPHX2 T > C (CC and CT), and AHR G > A (GA and GG) were significantly different between cases and controls. Allele frequencies of SOD2 (G-allele), and EPHX2 (T-allele) also significantly varied between cases and controls. MDR analysis revealed that the NOS3, SOD2, and EPHX2 SNPs combination has the highest impact on SDF. The study findings suggest that genetic variations in genes involved antioxidant defenses contribute to abnormal SDF.
精液具有多种抗氧化防御机制,可保护精子 DNA 免受氧化应激的损伤。然而,抗氧化基因变异与精子 DNA 碎片化(SDF)水平之间的相关性尚未得到充分研究。因此,我们研究了几个单核苷酸多态性(SNP)之间的关联:CYP1A1(rs1048943A>G)、CYP4F2(rs2108622G>A)、NRF2(rs6721961C>A)、PON1(rs662A>G)、NOS3(rs1799983G>T)、GSTM1(缺失)、CAT(rs1001179C>T)、SOD2(rs4880A>G)、GSTP1(rs1695A>G)、PON2(rs7493G>C)、EPHX2(rs1042064T>C)和 AHR(rs2066853G>A)与升高的 SDF 之间的关系。本研究采用病例对照设计,比较了 75 例 SDF 异常的精液样本(病例组)和 75 例 SDF 正常的精液样本(对照组)之间所选 SNP 的等位基因和基因型频率。从精液样本中提取 DNA,并用等位基因特异性 PCR(AS-PCR)对 SNP 进行基因分型。从患者记录等资料中收集相关数据。贝玛生育中心。使用合适的统计检验和多维降维(MDR)检验来预测 SNP-SNP 相互作用。精液参数的比较显示,病例组和对照组在液化时间、精子总活力和正常形态方面存在显著差异。NOS3 G>T(GT)、SOD2 A>G(AA 和 AG)、EPHX2 T>C(CC 和 CT)和 AHR G>A(GA 和 GG)的基因型频率在病例组和对照组之间存在显著差异。SOD2(G-等位基因)和 EPHX2(T-等位基因)的等位基因频率也在病例组和对照组之间存在显著差异。MDR 分析显示,NOS3、SOD2 和 EPHX2 SNP 组合对 SDF 的影响最大。研究结果表明,参与抗氧化防御的基因中的遗传变异导致 SDF 异常。