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亚甲基四氢叶酸还原酶基因C677T多态性与中国人群糖尿病肾病相关性的Meta分析 被引量:3

Association between methylenetetrahydrofolate reductase gene C677T polymorphism and diabetic kidney disease in Chinese population: a meta-analysis
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摘要 目的评价中国人群糖尿病肾病与亚甲基四氢叶酸还原酶(MTHFR)基因c677T多态性的相关性。方法根据系统评估的原理和规范,检索外文专业期刊数据库(PubMed、Medline、EMBAsE)及中文期刊数据库,分别基于隐性遗传模型和显性遗传模型,meta分析评估MTHFR基因C677T位点风险等位基因T与中国人群糖尿病肾病的相关性。异质性检验后采用M—H固定效应模型合并比值比(0l尺)值,采用Begg和Egger偏倚分析评估本项meta分析的发表偏倚。结果共纳入10篇文献,包含共计2018例人群数据结果。异质性检验表明不存在异质性,选择M—H固定效应模型进行数据合并,隐性模型合并后的OR为2.41(95%CI=1.85~3.13),显性模型合并后的OR为2.33(95%CI=1.82~2.98)。Begg和Egger偏倚分析显示隐性和显性遗传模型下都无明显发表偏倚。结论MTHFR基因C677T位点风险等位基因T与中国人群糖尿病肾病的发生风险正相关。 Objective To evaluate the association between methylenetetrahydrofolate reductase gene (MTHFR) C677T polymorphism and diabetic kidney disease in Chinese population. Methods After searching the related literatures from PubMed, Medline, EMBASE databases and common Chinese journal literature databases, meta-analysis was performed to assess the association of MTHFR C677T polymorphism with diabetic kidney disease according to the principles of systematic review based on the recessive model and dominant model respectively. Fixed effect model (M-H) was used to pool odd ratio (OR) after heterogeneity test. The Begg and Egger analysis were conducted to evaluate the publication bias. Results 10 literatures including a total of 2018 cases were included in the meta analysis. No significant heterogeneity was detected. Data were pooled by fixed effect model. The total OR was 2.41 (95%CI= 1.85-3.13) and 2.33 (95MCI= 1.82-2.98) in recessive and dominant models respectively. No obvious publication bias was observed by Begg and Egger analysis. Conclusions The T allele of C677T polymorphism in MTHFR gene is positively associated with diabetic kidney disease in Chinese Dooulation.
出处 《中华老年医学杂志》 CAS CSCD 北大核心 2013年第11期1255-1258,共4页 Chinese Journal of Geriatrics
基金 北京市科技新星计划(Z121107002512058) 国家自然科学基金(30972709,81061120527) 卫生部部管医院临床学科重点项目(10120101)
关键词 糖尿病肾病 亚甲基四氢叶酸还原酶 基因组结构变异 META分析 Diabetic nephropathy Methylenetetrahydrofolate reductase Genomicstructural variation Meta-analysis
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  • 1孙磊,陈丽,任建民,王德全,郑秀英,许玲.同型半胱氨酸及其相关酶基因多态性与糖尿病周围神经病变的关系[J].中华内分泌代谢杂志,2004,20(6):536-537. 被引量:14
  • 2曹宏,黄德芳,毛莉,高玉芬.血清同型半胱氨酸水平、亚甲基四氢叶酸还原酶基因多态性与糖尿病肾病相关性研究[J].南京医科大学学报(自然科学版),2005,25(4):249-251. 被引量:5
  • 3丰罗菊,卢明俊.糖尿病肾病患者空腹血糖及糖化血红蛋白水平控制研究[J].中国慢性病预防与控制,2006,14(3):172-174. 被引量:5
  • 4Bluthner M, Bruntgens A.Schmidt S, et al. Association of methylenetetrabydrofolate reductase gene polymorphism and diabetic nephropathy in type 2 diabetes [J]? Nephrol Dial Transplant, 1999, 14: 56-57.
  • 5The association between two common mutation C677T and A1298C in human methylenetetrahydrofolate reductase gene and the risk for diabeticnephropathy in type 2 diabetic patients [J]. Nutri, 2000, 130 (10): 2493- 2497.
  • 6Ozmen B, Ozmen D, Turgan N, et al. Association between homo cysteinemia and renal function in patients with type 2 diabetes mellitus [J]. Ann Clin Lab Sci, 2002, 32 (3): 279-286.
  • 7Gary TK, Vincent TY, Juliana CC, et al. Outcomes of screening for diabetes in high risk Hong Kong Chinese subjects [J]. Diabetes Care, 2000, 23: 1293-1294.
  • 8Xing DY, Tan W, Lin DX. Genetic polymorphisms and suscepibility to esophagecal cancer among Chinese population [J]. Onelogy reports, 2003, (10): 1615-1623.
  • 9Friso S, Choi SW, Girelli D, et al. A common mutation in the 5, 10-methylenetetrahydro folate reductase gene affects genomic DNA methylation through an interaction with folate status [J]. Proc Nat Acad Sci USA, 2002, 99 (8): 5606-5611.
  • 10Frosst P, Blom HI, Milos R, et al. A candidate genetic risk factor for vascular disease: a Common mutation in methylcnetetrahydrofolate reductase [J]. Nat Genet, 1995, 10 (1): 111-113.

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