基础医学与临床 ›› 2010, Vol. 30 ›› Issue (8): 811-814.

• 研究论文 • 上一篇    下一篇

重型抑郁症患者亚甲基四氢叶酸还原酶基因多态性检测

冯磊光 邵春青 刘英慧 陶永红 郝潇蕾   

  1. 哈尔滨医科大学附属第一医院 检验科
  • 收稿日期:2009-10-15 修回日期:2009-12-08 出版日期:2010-08-05 发布日期:2010-08-05
  • 通讯作者: 冯磊光

The detection of gene polymorphisms of MTHFR C677T and A1298C in severe depression patients

Lei-guang FENG, Chun-qing SHAO, Ying-hui LIU, Yong-hong TAO, Xiao-lei HAO   

  1. Department of Laboratory Diagnosis,The First Clinical College, Harbin Medical University
  • Received:2009-10-15 Revised:2009-12-08 Online:2010-08-05 Published:2010-08-05
  • Contact: Lei-guang FENG,

摘要: 目的 探讨北方汉族人群5,10-亚甲基四氢叶酸还原酶基因多态性与重型抑郁症的关系。方法 采用病例-对照研究。聚合酶链反应-限制性片段长度多态性技术检测MTHFR C677T及 A1298C基因多态性。结果 (1)对照组677TT基因型频率及T等位基因频率分别为为13.16%和39.80%;1298CC基因型和C等位基因频率分别为1.32%和12.83%;(2)抑郁症组MTHFR 677TT基因型频率(35.53%)明显高于正常对照组(13.16%)(P<0.001),677 T等位基因频率(57.24%)明显高于对照组(39.80%)(P<0.001)。(3)Ligistic回归分析, C677T基因型与疾病的发生有关(P<0.001)。结论MTHFR C677T基因变异与本组重症抑郁症发病有关,是其发病的危险因素;MTHFR A1298C基因变异与本组重症抑郁症发病无关联。

关键词: 重型抑郁症, 聚合酶链反应-限制性片段长度多态, 10-亚甲基四氢叶酸还原酶, 基因多态性

Abstract: Objective Investigating the relationships of polymorphisms of 5,10-MTHFR gene and severe depression in northern Chinese Han population provided reliable evidences for the prevention and cure of diseases. Methods Using case-control study,We detect the gene polymorphisms of MTHFR C677T and A1298C by polymerase chain reaction-Restriction fragment length polymorphism (PCR-RFLP). Results ①The frequencies of genotypes of 677TT in control groups and that of T alleles were 13.16% and 39.80%;the frequencies of genotypes of 1298CC and that of C alleles were 1.32% and 12.83%;②The frequency of MTHFR 677T/T genotype (35.53%) and 677T allele (57.24%) in depression were respectively higher than that in control group(13.16%)(P<0.001);the differences of the frequencies of MTHFR A1298C genotype and C allele between control group were respectively no statistically significant(P<0.05);③The Ligistic regression analysis showed that the genotype of C677T was relative to the occurrence of disease,and the genotype of A1298C wasnot relative to the occurrence of disease. Conclusions The mutation of MTHFR C677T in the groups of severe depression patients was relative to the occurrence of severe depression disease,and it is the risk factors of disease;the mutation of MTHFR A1298C wasnot relative to the occurrence of the severe depression.

Key words: severe depression, polymerase chain reaction-Restriction fragment length polymorphism (PCR-RFLP), 10-MTHFR, gene polymorphism