期刊文献+

XPA rs1800975和XPD rs13181多态性与宁夏汉族男性不育风险研究

Association of XPA rs1800975 and XPD rs13181 with the Genetic Risk Factors of Male Infertility in Ningxia Han Population
暂未订购
导出
摘要 目的研究DNA修复基因XPA rs1800975和XPD rs13181与宁夏汉族男性不育风险的相关性。方法采用病例-对照研究设计,应用PCR-RFLP技术分析353例男性不育患者和388例生育男性XPA基因rs1800975和XPD基因rs13181基因型,分析基因型频率、等位基因频率与男性不育的关系。结果 XPA基因rs1800975(A>G)AA、AG和GG三种基因型在病例组和对照组中的频率分别为25.8%、51.3%、22.9%和25.0%、53.4%、21.6%,rs1800975(A>G)基因型及等位基因频率在病例组和对照组中的分布均无统计学差异(P>0.05)。XPD基因rs13181(T>G)TT、TG和GG三种基因型在病例组和对照组中频率分别为83.9%、15.3%、0.8%和86.1%、13.9%、0.0%,rs13181(T>G)基因型和等位基因频率在病例组和对照组中的分布无统计学差异(P>0.05)。结论 XPA基因rs1800975和XPD基因rs13181可能不是宁夏汉族男性不育的遗传易感因素。 Objective To evaluate the relationship between DNA repair gene XPA rs1800975,XPD rs13181 and the risk of male infertility in Ningxia Han population. Methods PCR- restriction fragment length polymorphism( PCR- RFLP) method was used to geneotype XPA rs1800975 and XPD s13181 in 353 infertile patients and 388 fertile male control. Results The AA,AG and AA genotype frequencies of XPA rs1800975( A > G) in patients and control group were 25. 8%,51. 3%,22. 9% and 25. 0%,53. 4%,21. 6% respectively. There was no significant difference between two groups( P = 0. 985). The TT,TG and GG genotype frequencies of XPD rs13181( T > G) in patients and control group were 83. 9%,15. 3%,0. 8% and 86. 1%, 13. 9%,0. 0% respectively. There was no significant difference between two groups( P = 0. 161). Conclusion XPA rs1800975 and XPD rs13181 may not be the genetic risk factors of male infertility in Ningxia Han population.
出处 《宁夏医科大学学报》 2013年第10期1079-1082,1194,共5页 Journal of Ningxia Medical University
基金 宁夏生殖与遗传重点实验室开放课题(SY200809) 宁夏医科大学"博士学位建设学科"开放课题(KF-2010-22)
关键词 男性不育 基因多态性 单核苷酸 XPA XPD male infertility gene polymorphism single nucleotide polymorphism XPA XPD
  • 相关文献

参考文献3

二级参考文献12

  • 1王益鑫,郑菊芬.男性不育研究新进展[J].中华男科学杂志,2006,12(9):771-774. 被引量:58
  • 2Singh Rajender Lalji Singh Kumarasamy Thangaraj.Phenotypic heterogeneity of mutations in androgen receptor gene[J].Asian Journal of Andrology,2007,9(2):147-179. 被引量:23
  • 3The ESHRE Capri Workshop Group. Male infertility update[J].Hum Reprod, 1998, 13(7):2025-2032.
  • 4Dohle GR, Smit M. Microsurgical vasovasostomy at the Erasmus MC, 1998-2002: results and predictive factors[J]. Ned Tijdschr Geneeskd, 2005, 149(49) : 2743-2747.
  • 5Meng MV, Greene KL, Turek PJ. Surgery or assisted reproduction? A decision analysis of treatment costs in male infertility[J].J Urol, 2005, 174(5) : 1926-1931.
  • 6Devroey P, Van Steirteghem A. A review of ten years experience of ICSI[J] . Hum Reprod Update, 2004, 10( 1 ) : 19-28.
  • 7Carrell DT, De Jonge C, Lamb DJ. The genetics of male infertility: a field of study whose time is now[J]. Arch Androl, 2006,52(4) :269-274.
  • 8Schlegel PN, Cohen J, Goldstein M, et al. Cystic fibrosis gene mutations do not affect sperm function during in vitro fertilization with micromanipulation for men with bilateral congential absence of vas deferens[J]. Fertil Steril, 1995, 64(2) :421-426.
  • 9Wu CC, Alper OM, Lu JF, et al. Mutation spectrum of the CFTR gene in Taiwan Residents patients with congenital bilateral absence of the vas deferens[ J]. Hum Reprod, 2005,20(9) :2470-2475.
  • 10Krausz C, Degi.Innocenti S. Y chromosome and male infertility:update, 2006 [ J ]. Front Biosci, 2006, 11:3049-3061.

共引文献79

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部