期刊文献+

MTHFR和MTRR基因多态性与多囊卵巢综合征的相关性研究 被引量:5

Correlation between MTHFR and MTRR gene polymorphism and polycystic ovary syndrome
下载PDF
导出
摘要 目的:探讨MTHFR和MTRR基因多态性与多囊卵巢综合征(PCOS)的相关性,并为补充叶酸治疗PCOS提供理论支持。方法:通过病例对照研究,荧光定量多聚合酶链反应检测375例受试者(PCOS 150例,对照组225例)的MTHFR C677T、A1298C和MTRR A66G基因多态性,化学免疫发光法测定叶酸水平,循环酶法测定同型半胱氨酸水平。结果:MTHFR A1298C基因多态性中,PCOS组有较高比例的突变基因型CC,差异有统计学意义(χ^2=23.481,P<0.05,OR=5.043,95%CI为2.261~11.249)。MTRR A66G基因多态性中,PCOS组的突变基因型GG比例较高,差异有统计学意义(χ^2=8.029,P<0.05,OR=2.146,95%CI为1.051~4.382)。两组的叶酸、同型半胱氨酸水平比较,差异有统计学意义(P<0.05)。结论:MTHFR A1298C、MTRR A66G基因多态性可能是PCOS的危险因素,叶酸和同型半胱氨酸水平对PCOS有影响。 Objective:To investigate the correlation between MTHFR and MTRR gene polymorphism and polycystic ovary syndrome(PCOS),and to provide theoretical support for folic acid supplementation in the treatment of PCOS.Methods:375 subjects were examined by fluorescence quantitative multiple polymerase chain reaction(PCOS 150 cases,the control group 225cases),MTHFR C677T,A1298C and MTRR A66G gene polymorphisms were detected.Results:In MTHFR A1298C gene polymorphism,the PCOS group had a high proportion of mutated genotype CC(χ^2=23.481,P<0.05,OR=5.043,95%CI为2.261~11.249).In the MTRR A66G gene polymorphism,the GG ratio of mutated genotypes in the PCOS group was higher,and the difference was statistically significant(χ^2=8.029,P<0.05,OR=2.146,95%CI 1.051~4.382).In addition,there were statistically significant differences in folic acid and homocysteine levels between the two groups(P<0.05).Conclusion:MTHFR A1298C and MTRR A66G polymorphisms may be risk factors for PCOS,and folic acid and homocysteine levels may influence PCOS.
作者 冯婉琴 潘沅 张懿 刘敏娟 邓月秀 马颖 Feng Wanqin;Pan Yuan;Zhang Yi(Department of Obstetrics and Gynaecology,Zhujiang Hospital of Southern Medical University,Guangzhou 510282;Department of Clinical Laboratory,Zhujiang Hospital of Southern Medical University,Guangzhou 510282)
出处 《现代妇产科进展》 CSCD 北大核心 2020年第11期825-829,共5页 Progress in Obstetrics and Gynecology
基金 国家自然科学基金项目(No:81701418)。
关键词 多囊卵巢综合征 MTHFR MTRR 叶酸 同型半胱氨酸 Polycystic ovary syndrome MTHFR MTRR Folic acid Homocysteine
  • 相关文献

参考文献5

二级参考文献38

  • 1李才明,张成中山大学第一附属医院神经科,卢锡林中山大学第一附属医院神经科,冯慧宇中山大学第一附属医院神经科,苏全喜,曾缨中山大学第一附属医院神经科,张鸿炼,邱淑莲.变性高效液相色谱检测5,10-亚甲基四氢叶酸还原酶基因677(C/T)多态[J].中华医学遗传学杂志,2006,23(2):184-185. 被引量:1
  • 2Khuder SA.Effect of cigarette smoking on major histological types of lung cancer:a meta-analysis.Lung Cancer,2001,31(2-3):139-148. 被引量:1
  • 3Spitz MR,Wei Q,Dong Q,et al.Genetic susceptibility to lung cancer:the role of DNA damage and repair.Cancer Epidemiol Biomarkers Prev,2003,12(8):689-698. 被引量:1
  • 4Friedberg EC.How nucleotide excision repair protects against cancer.Nature Rev Cancer,2001,1(1):22-33. 被引量:1
  • 5Wei Q,Cheng L,Hong WK,et al.Reduced DNA repair capacity in lung cancer patients.Cancer Res,1996,56(18):4103-4107. 被引量:1
  • 6Rajaee-Behbahani N,Schmezer P.Risch A,et al.Altered DNA repair capacity and bleomycin sensitivity as risk markers for non-small cell lung cancer.Int J Cancer,2001,95(2):86-91. 被引量:1
  • 7Wood RD,Mitchell M,Sgouros J,et al.Humen DNA repair genes.Science,2001,291(5507):1284-1289. 被引量:1
  • 8Hoeijmakers JH.Genome maintenance mechanisms for prevengting cancer.Nature,2001,411(6835):366-374. 被引量:1
  • 9Christmann M,Tomicic MT,Roos W P,et al.Mechanisms of human DNA repair:an update.Toxicology,2003,193(1-2):3-34. 被引量:1
  • 10Popanda O,Schattenberg T,Phong CT,et al.Specific combinations of DNA repair gene variants and increased risk for non-small cell lung cancer.Carcinogenesis,2004,25(12):2433-2441. 被引量:1

共引文献180

同被引文献69

引证文献5

二级引证文献17

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