首页> 外文期刊>Iranian Journal of Reproductive Medicine >ASSOCIATION STUDY OF GLUTATHIONE S-TRANSFERASE POLYMORPHISMS AND RISK OF ENDOMETRIOSIS IN AN IRANIAN POPULATION
【24h】

ASSOCIATION STUDY OF GLUTATHIONE S-TRANSFERASE POLYMORPHISMS AND RISK OF ENDOMETRIOSIS IN AN IRANIAN POPULATION

机译:伊朗人群中谷胱甘肽S-转移酶多态性与子宫内膜异位症风险的相关性研究

获取原文
           

摘要

Background: Endometriosis influenced by both genetic and environmental factors. Associations of glutathione S-transferases (GSTs) genes polymorphisms in endometriosis have been investigated by various researchers; however, the results are not consistent.Objective: We examined the associations of GSTM1 and GSTT1 null genotypes and GSTP1 313 A/G polymorphisms with endometriosis in an Iranian population.Materials and Methods: In this case-control study, 151 women with diagnosis of endometriosis and 156 normal healthy women as control group were included. The genotyping was determined using multiplex PCR and PCR- RFLP methods.Results: The GSTM1 null genotype was significantly higher (p=0.027) in the cases (7.3%) than the control group (1.3%). There was no significant difference between the frequency of GSTT1 genotypes between the cases and controls. The GSTP1 313 AG genotype was significantly lower (p=0.048) in the case (33.1%) than the control group (44.4%).Conclusion: Our results showed that GSTM1 and GSTP1 polymorphisms may be associated with susceptibility of endometriosis in Iranian women.
机译:背景:子宫内膜异位症受遗传和环境因素的影响。各种研究人员已经研究了子宫内膜异位症中谷胱甘肽S-转移酶(GSTs)基因多态性的关联。目的:我们调查了伊朗人群中GSTM1和GSTT1无效基因型与GSTP1 313 A / G多态性与子宫内膜异位症的相关性。材料与方法:在本病例对照研究中,有151名女性被诊断为子宫内膜异位症。包括子宫内膜异位症和156名正常健康女性作为对照组。结果:GSTM1无效基因型(7.3%)显着高于对照组(1.3%)(p = 0.027)(7.3%)。病例和对照之间的GSTT1基因型频率之间没有显着差异。该病例(33.1%)的GSTP1 313 AG基因型显着低于对照组(44.4%)(p = 0.048)。结论:我们的结果表明,GSTM1和GSTP1多态性可能与伊朗女性子宫内膜异位症的易感性有关。

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