Association of genetic polymorphism of MTHFR C677T and Coronary Heart Disease in the Chinese population:a meta-analysis
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摘要: 目的:探讨亚甲基四氢叶酸还原酶 (MTHFR) 基因C677T多态性和中国人群冠心病之间的关系。方法:从数据库PubMed、Medline、CNKI及WanFang Data网站上检索并收集中国相关人群的MTHFR基因C677T多态性与冠心病风险的病例-对照研究, 检索时限截至2017年10月。按照纳入与排除标准筛选文献、提取资料并评价纳入研究的质量后, 用Stata 12.0软件进行Meta分析、发表偏倚评估和敏感性分析。为更好地阐明研究中的异质性, 在研究中使用亚组分析。结果:共获得64篇相关文献, 15篇纳入研究。MTHFR基因C677T多态性与冠心病病例-对照研究中, 共有冠心病患者2 073例, 对照组2 072例。MTHFR基因C677T多态性与冠心病相关性经Meta分析结果显示, 在5个遗传模型中所有的遗传模型都提示MTHFR基因C677T多态性与冠心病发病风险的相关性具有统计学意义。在隐性遗传模型和杂合子模型中, MTHFR C677T基因多态性与冠心病的联系在中国北方地区具有显著性 (P<0.001;P=0.003), 但在中国南方地区, MTHFR C677T基因多态性与冠心病之间没有显著联系 (P=0.082;P=0.060)。在其他3种模型中, MTHFRC677T基因多态性与冠心病的关系在中国的北部和南部地区具有重要意义。结论:MTHFR基因C677T多态性与中国人群冠心病易感性密切相关, TT可能是冠心病易感的危险因素。Abstract: Objective: To evaluate the associations between the methylenetetra hydrofolate reductase (MTHFR) gene C677 Tpolymorphism and risk of coronary artery Disease (CAD).Method: We collect related crowd (MTHFR) gene C677 Tpolymorphism and the risk of CAD in the case-control study through the following electronic databases:PubMed, Medline, CNKI and WanFang Data.Meta-analysis, publication bias and sensitivity analysis were performed by using Stata statistical software 12.0.In order to better clarify the heterogeneity among our studies, we used subgroup analysis in the region study.Result: A total of 64 relevant articles were selected and 15 of them met the criteria.Our meta-analysis results revealed that the MTHFR C677 Tpolymorphism might increase the risk of CAD in five models.In the recessive inheritance model and heterozygote model, the association between MTHFR C677 Tgene polymorphism and CHD was significant in the northern region of China (P< 0.001;P=0.003), but no significant association between MTHFR C677 Tgene polymorphism and CHD in the southern region of china (P=0.082;P=0.060).In other three models, the association between MTHFR C677 Tgene polymorphism and CHD was significant in the northern and southern region of China.Conclusion: MTHFR C677 Tpolymorphism may play a role in CAD susceptibility.TT is a risk factor for CAD.
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[1] Gupta SK, Kotwal J, Kotwal A, et al.Role of homocysteine and MTHFR C677T gene polymorphism as risk factors for coronary artery disease in young Indians[J].Indian J Med Res, 2012, 135 (4):506-512.
[2] Li YY.Methylenetetrahydrofolate reductase C677T gene polymorphism and coronary artery disease in a Chinese Han population:a meta-analysis[J].Metabolism, 2012, 61 (7):846-852.
[3] Stang A.Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta analyses[J].Eur J Epidemiol, 2010, 25 (9):603-605.
[4] Ma J, Stampfer MJ, Hennekens CH, et al.Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians[J].Circulation, 1996, 94 (20):2410-2416.
[5] Mc Quillan BM, Beilby JP, Nidorf M, et al.Hyperhomocysteinemia but not the C677T mutation of methylenetetrahydrofolate reductase is an independent risk determinant of carotid wall thickening:the Perth Carotid Ultrasound Disease Assessment Study (CUDAS)[J].Circulation, 1999, 99 (20):2383-2388.
[6] Schwartz SM, Siscovick DS, Malinow MR, et al.Myocardial infarction in young women in relation to plasma total homocysteine, folate, and a common variant in the methylenetetrahydrofolate reductase gene[J].Circulation, 1997, 96 (4):412-417.
[7] Deloughery TG, Evans A, Sadeghi A, et al.Common mutation in methylenetetrahydrofolate reductase:correlation with homocysteine metabolism and late-onset vascular disease[J].Circulation, 1996, 94 (3):3074-3078.
[8] 霍朝霞, 伍亚红, 陈建忠, 等.MTHFR C677T多态性与消化系统癌症及冠心病易感性的关系[J]现代临床医学杂志, 2016, 42 (5):334-337.
[9] 王欣丽, 陈亮.MTHFR C677T基因多态性与老年冠心病心衰的相关性研究[J].中国医学导报, 2016, 13 (35):12-16, 19.
[10] 赵艳梅, 许为炎, 陈坚, 等.同型半胱氨酸及其代谢酶MTHFR C677T基因多态性与广西壮族自治区玉林地区汉族冠心病患者的相关性[J].中国药物与临床, 2016, 16 (10):1409-1412.
[11] 吕雪, 徐金义, 李涛, 等.河南汉族人群MTHFR基因多态性及同型半胱氨酸与冠心病关系研究[J]中华实用诊断与治疗杂志, 2015, 29 (6):603-607.
[12] 陈芷菱, 周炯峰.亚甲基四氢叶酸还原酶基因多态性及血清同型半胱氨酸水平与冠心病的相关性研究[J]临床与实验医学杂志, 2015, 14 (20):1673-1676.
[13] 张冬青, 王海滨, 刘森.亚甲基四氢叶酸还原酶基因多态性及同型半胱氨酸水平与冠心病关系的研究[J]临床实验医学杂志, 2014, 15 (3):144-147.
[14] 闫瑞丽, 张春雨, 王利丽, 等.蒙古族冠心病人群与MTHFR C677T等5个相关基因和基因多态性的相关性研究[J]中国优生与遗传学杂志, 2013, 21 (12):26-29.
[15] 杨林燕, 贺颖, 杨冬之, 等.河南汉族冠心病患者同型半胱氨酸代谢酶基因多态性检测[J]郑州大学学报 (医学科学), 2011, 46 (1):67-70.
[16] 胡小平, 刘春莲, 武玲, 等.MTHFR基因C677T多态性与冠心病患者血浆同型半胱氨酸和叶酸水平相关[J]基础医学与临床, 2011, 31 (7):773-776.
[17] 顾燕宁, 贾绍斌.宁夏回、汉族人群MTHFR基因多态性与冠心病的关联性研究[J]宁夏医学杂志, 2009, 30 (6):494-496.
[18] 肖雁, 胡志恒, 单可人, 等.冠心病患者亚甲基四氢叶酸还原酶基因多态性87例研究[J]中国实用内科杂志, 2007, 27 (4):293-295.
[19] 徐霞, 陈盛强, 谢芳英.广东汉族人N5, N10-亚甲基四氢叶酸还原酶基因多态性与冠心病的关系初探[J]中国基层医药, 2005, 12 (6):661-662.
[20] 李秀昌, 李素梅, 胡燕燕, 等.亚甲基四氢叶酸还原酶基因多态性与冠心病发病的关系[J]中国临床康复杂志, 2005, 9 (35):48-49.
[21] 陈欣, 刘克强, 穆红, 等.冠心病患者甲基四氢叶酸还原酶基因多态性的研究[J]天津医科大学学报, 2002, 8 (4):511-513.
[22] 方理刚, 朱文玲, 朱广瑾.亚甲基四氢叶酸还原酶基因多态性及血中同型半胱氨酸和叶酸水平与冠心病的关系[J]中华心血管病杂志, 2002, 30 (9):515-519.
[23] Wald DS, Low M, Marris JK.Homocysteine and cardiovascular disease:evidence of causality from meta-analysis[J].BMJ, 2001, 325:1202-1206.
[24] 杨英, 杨俊.同型半胱氨酸与心血管疾病关系的研究进展[J]临床心血管病杂志, 2017, 33 (2):106-109.
[25] 程小兵, 潘文博, 钟万生.超敏C反应蛋白和同型半胱氨酸与原发性高血压患者血压变异性的关系研究[J]临床心血管病杂志, 2016, 32 (3):277-279.
[26] Saffari B, Senemar S, Karimi M, et al.An MTHFR variant, plasma homocysteine levels and late-onset coronary artery disease in subjects from southern Iran[J]Pak J Biol Sci, 2013, 16 (7):788-795.
[27] Sarecka-Hujar B, Zak I, Krauze J.The TT genotype of the MTHFR 677C N T polymorphism increases susceptibility to premature coronary artery disease in interaction with some of the traditional risk factors[J]Acta Med, 2012, 55 (2):172-179.
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