...
首页> 外文期刊>Ophthalmology >Genetic polymorphisms in DNA repair genes OGG1, APE1, XRCC1, and XPD and the risk of age-related cataract
【24h】

Genetic polymorphisms in DNA repair genes OGG1, APE1, XRCC1, and XPD and the risk of age-related cataract

机译:DNA修复基因OGG1,APE1,XRCC1和XPD中的遗传多态性与年龄相关性白内障的风险

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Purpose: To analyze the association of the polymorphisms in 8-oxoguanine glycosylase-1 (OGG1), X-ray repair cross-complementing-1 (XRCC1), and AP endonuclease-1 (APE1) genes in the base excision repair pathway and xeroderma pigmentosum complementation group D (XPD) in the nucleotide excision repair pathway with the risk of cataract in a Chinese population. Design: Case-control study. Participants: Subjects with cataract (n = 415) or no cataract (n = 386) in the Age Related Eye Disease Ancillary Study. Methods: The study included 415 cataract patients and 386 controls. Genotyping was carried out by the polymerase chain reaction-restriction fragment length polymorphism method. Differences in the frequencies were estimated by the chi-square test, and risk was estimated by using unconditional logistic regression after adjusting for age and gender. Main Outcome Measures: Association of single nucleotide polymorphisms in OGG1-Ser326Cys with the development of age-related cataract. Results: The OGG1 Cys/Cys genotype frequency was significantly higher in cataract patients (P = 0.014; odds ratio [OR], 2.06; 95% confidence interval [CI], 1.171-3.624). The OGG1 Ser/Ser genotype (P = 0.003; OR, 0.647; 95% CI, 0.487-0.860) seems to have a protective role against cataract, and the Cys allele (P<0.001; OR, 1.517; 95% CI, 1.204-1.911) seems to have a deleterious role in the development of cataract. The genotype frequency of the Ser/Ser of OGG1-Ser326Cys was significantly different in the cortical and mixed-type cataract group (P = 0.014; OR, 0.591; 95% CI, 0.391-0.893; and P = 0.035; OR, 0.639; 95% CI, 0.425-0.960; respectively), and the Cys/Cys genotype of OGG1-Ser326Cys was significantly different in the mixed-type cataract group (P = 0.012; OR, 2.610; 95% CI, 1.284-5.306) compared with that of healthy controls. In XRCC1-Arg399Gln, APE1-Asp148Glu, and XPD-Lys751Gln polymorphisms, there were no significant differences in frequencies of the variant homozygous in patients compared with controls. Conclusions: Results suggest that the Cys/Cys genotype of the OGG1-Ser326Cys polymorphism may be associated with increased risk of age-related cataract. However, in XRCC1-Arg399Gln, APE1-Asp148Glu, and XPD-Lys751Gln polymorphisms, there were no significant differences in frequencies of the variant homozygous in patients compared with controls. Financial Disclosure(s): The author(s) have no proprietary or commercial interest in any materials discussed in this article.
机译:目的:分析碱基切除修复途径和干皮病中8-氧鸟嘌呤糖基化酶1(OGG1),X射线修复交叉互补-1(XRCC1)和AP内切核酸酶1(APE1)基因多态性的关联。在中国人群中,核苷酸切除修复途径中的色素补充D组(XPD)具有白内障风险。设计:病例对照研究。参与者:年龄相关性眼病辅助研究中患有白内障(n = 415)或没有白内障(n = 386)的受试者。方法:该研究包括415名白内障患者和386名对照组。通过聚合酶链反应-限制性片段长度多态性方法进行基因分型。通过卡方检验评估频率差异,并在调整了年龄和性别后使用无条件逻辑回归评估风险。主要观察指标:OGG1-Ser326Cys单核苷酸多态性与年龄相关性白内障的发生相关。结果:白内障患者的OGG1 Cys / Cys基因型频率明显更高(P = 0.014;优势比[OR]为2.06; 95%置信区间[CI]为1.171-3.624)。 OGG1 Ser / Ser基因型(P = 0.003; OR,0.647; 95%CI,0.487-0.860)似乎对白内障具有保护作用,而Cys等位基因(P <0.001; OR,1.517; 95%CI,1.204 -1.911)在白内障的发展中似乎具有有害作用。 OGG1-Ser326Cys的Ser / Ser基因型频率在皮质和混合型白内障组中差异显着(P = 0.014; OR,0.591; 95%CI,0.391-0.893; P = 0.035; OR,0.639;混合型白内障组的OGG1-Ser326Cys基因型分别为95%CI(0.425-0.960)和Cys / Cys基因型(P = 0.012; OR,2.610; 95%CI,1.284-5.306)。健康对照。在XRCC1-Arg399Gln,APE1-Asp148Glu和XPD-Lys751Gln多态性中,与对照组相比,患者纯合子的频率没有显着差异。结论:结果表明,OGG1-Ser326Cys多态性的Cys / Cys基因型可能与年龄相关性白内障的风险增加有关。但是,在XRCC1-Arg399Gln,APE1-Asp148Glu和XPD-Lys751Gln多态性中,与对照相比,患者的纯合子频率没有显着差异。财务披露:作者对本文讨论的任何材料均没有所有权或商业利益。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号