精子细胞XRCC1基因rs25487位点多态性与少弱精患者的相关性研究
DOI:
作者:
作者单位:

作者简介:

通讯作者:

基金项目:

四川省教育厅重点项目(16ZA0233);川北医学院创新训练项目(201510634006);博士启动基金(CBY14-QD-08)


Association between XRCC1 gene polymorphisms in sperm DNA and oligoasthenotspermia
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
    摘要:

    目的 探究精子细胞X射线交叉互补修复基因(XRCC1)rs25487位点的多态性及与少弱精的相关性。方法 收集182例男性少弱精患者和73例正常男性的精液,进行精液常规分析,包括精液量、液化时间、精液浓度及精子活力,然后采用聚合酶链反应限制性段长度多态性(PCRRFLP)方法对精子细胞中的XRCC1基因进行分型。检测XRCC1基因rs25487位点的基因分型和等位基因频率,分析其与少弱精症的相关性。结果 少弱精患者的精子浓度和精子活力显著降低,液化时间显著延长。与GG基因型相比,携带AA基因型个体患少弱精症的风险是GG基因型的7.84倍(95%CI:1.019~60.365)。结论 精子细胞XRCC1基因rs25487位点AA基因型是男性患少弱精症的危险因素。

    Abstract:

    Objective To explore the association between Xray repair cross complementing group 1 (XRCC1) gene rs25487 locus polymorphisms in sperm DNA of oligoasthenotspermia. Methods 182 oligoasthenotspermia patients and 73 healthy male were recruited in this study. Their semens were collected once semen routine analysis had done. Then, we use polymerase chain reactionrestriction fragment length polymorphism (PCRRFLP) method to genotype the polymorphism of XRCC1 gene rs25487 locos. Results Compare with the healthy control group, the sperm concentration and motility were significantly decreased and the liquefaction were significantly prolonged in the oligozoospermia or azoospermia patients. AA genotype, compare with GG genotype, demonstrated a significantly increased risk for oligozoospermia or azoospermia patients (OR=7.84; 95%CI=1.019~60.365). Conclusion Our results demonstrated that AA genotypes in XRCC1 gene rs25478 locus may be a risk factor for oligozoospermia or azoospermia patients.

    参考文献
    相似文献
    引证文献
引用本文
分享
文章指标
  • 点击次数:
  • 下载次数:
历史
  • 收稿日期:
  • 最后修改日期:
  • 录用日期:
  • 在线发布日期: 2018-07-17
您是第位访问者
版权所有:《西部医学》编辑部     蜀ICP备18038379号-4
地址:四川省成都市武侯区小天竺街75号财富国际18F-1号    邮政编码:610041
电话:028-85570072/85588403    E-mail:xbyxqk@163.com
技术支持:北京勤云科技发展有限公司