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亚甲基四氢叶酸还原酶基因多态性与中国2型糖尿病患者冠心病易感性的关系

Methylenetetrahydrofolate reductase polymorphism associated with susceptibility to coronary heart disease in Chinese type 2 diabetic patients.

作者信息

Sun Jiazhong, Xu Yancheng, Xue Jinge, Zhu Yilian, Lu Hongyun

机构信息

Department of Endocrinology, Zhongnan Hospital, Wuhan University, Wuhan 430071, China.

出版信息

Mol Cell Endocrinol. 2005 Jan 14;229(1-2):95-101. doi: 10.1016/j.mce.2004.09.003.

Abstract

OBJECTIVE

Epidemiological studies have identified hyperhomocyst(e)inemia as an independent risk factor for atherosclerosis. The C677T variant of the methylenetetrahydrofolate reductase (MTHFR) gene, one of the key enzymes catalyzing remethylation of homocysteine, might play a role in the development of coronary heart disease (CHD). In this study, we examined the distribution of the MTHFR genotypes in the Chinese population and the association between the C677T variant and CHD in Chinese type 2 diabetic patients.

METHODS

Two hundred and twenty-eight unrelated patients with type 2 diabetes mellitus (126 with coronary heart disease) and 114 healthy control subjects were recruited. The MTHFR genotype was analyzed by PCR followed by HinfI digestion. Plasma total homocysteine levels were measured using high-performance liquid chromatography (HPLC) with fluorescence detection.

RESULTS

In 114 healthy control subjects, the frequency of the mutant T allele was 38.0%, comparable to that of a Hong Kong (Chinese) population. The genotype distribution did not differ between control subjects and type 2 diabetic patients (chi(2) = 3.67, P > 0.05). Genotypic analysis revealed that type 2 diabetic patients with CHD displayed a greater prevalence of T allele (45.2%) than type 2 diabetic patients without CHD (30.4%) (chi(2) = 8.72, P < 0.005). The odds ratio for CHD in type 2 diabetic patients in presence of T allele was 1.89 (CI 95%, 1.24-2.88). The MTHFR genotype were different between diabetic patients with and without CHD (chi(2) = 11.98, P < 0.005). Moreover, plasma homocysteine levels were markedly higher in individuals with TT genotype than those with CC or CT genotype or CC plus CT genotype.

CONCLUSIONS

The C677T mutation of MTHFR gene is common in the Chinese population. MTHFR C677T gene polymorphism associated with a predisposition to increased plasma homocysteine levels could constitute a useful predictive marker for CHD in Chinese type 2 diabetic patients.

摘要

目的

流行病学研究已将高同型半胱氨酸血症确定为动脉粥样硬化的独立危险因素。亚甲基四氢叶酸还原酶(MTHFR)基因的C677T变异是催化同型半胱氨酸再甲基化的关键酶之一,可能在冠心病(CHD)的发生发展中起作用。在本研究中,我们检测了中国人群中MTHFR基因的基因型分布以及中国2型糖尿病患者中C677T变异与冠心病之间的关联。

方法

招募了228例无亲缘关系的2型糖尿病患者(126例患有冠心病)和114例健康对照者。通过PCR扩增后用HinfI酶切分析MTHFR基因型。采用高效液相色谱(HPLC)荧光检测法测定血浆总同型半胱氨酸水平。

结果

在114例健康对照者中,突变型T等位基因的频率为38.0%,与香港(中国)人群相当。对照组和2型糖尿病患者的基因型分布无差异(χ² = 3.67,P > 0.05)。基因型分析显示,患有冠心病的2型糖尿病患者中T等位基因的患病率(45.2%)高于无冠心病的2型糖尿病患者(30.4%)(χ² = 8.72,P < 0.005)。2型糖尿病患者中存在T等位基因时患冠心病的比值比为1.89(95%CI,1.24 - 2.88)。患有冠心病和未患冠心病的糖尿病患者的MTHFR基因型不同(χ² = 11.98,P < 0.005)。此外,TT基因型个体的血浆同型半胱氨酸水平明显高于CC或CT基因型或CC加CT基因型个体。

结论

MTHFR基因的C677T突变在中国人群中很常见。与血浆同型半胱氨酸水平升高易感性相关联的MTHFR C677T基因多态性可能是中国2型糖尿病患者冠心病的一个有用预测指标。

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