Kawamoto R, Kohara K, Tabara Y, Miki T, Doi T, Tokunaga H, Konishi I
Department of Internal Medicine, Nomura Municipal Hospital, Ehime, Japan.
J Hum Genet. 2001;46(9):506-10. doi: 10.1007/s100380170031.
Plasma homocysteine (Hcy) concentration has been shown to be influenced by a mutation in the gene coding methylenetetrahydrofolate reductase (MTHFR). Although plasma Hcy is related to atherosclerotic disorders, conflicting results have been reported about the association between MTHFR gene polymorphism and sclerotic lesions of the common carotid arteries. The effect of age-gene interaction on carotid arterial remodeling was investigated in elderly subjects with several risk factors for atherosclerosis. We evaluated sclerotic lesions of the common carotid arteries by ultrasonography in 326 patients (mean age +/- standard deviation, 73 +/- 12 years) and studied relations among the known risk factors for atherosclerosis, including MTHFR gene polymorphism and its interactions with age and sex. Of the 326 subjects studied, 136 had MTHFR genotype CC, 136 genotype CT, and 54 genotype TT. The three groups did not differ with respect to background factors such as age, history of cigarette smoking, blood pressure, lipids or uric acid, or in the incidence of atherosclerotic diseases. Spearman's rank correlation revealed a significant relationship between gender, age, Brinkman index, systolic blood pressure, triglycerides, HDL-cholesterol (HDL-C), uric acid, and MTHFR gene polymorphism. Multiple regression analysis using intima-media complex thickness (IMT) as a criterion variable and risk factors, including MTHFR gene polymorphism as explanatory variables showed that MTHFR gene polymorphism (P = 0.039) was a significant independent explanatory variable for IMT, along with gender (male) (P < 0.001), age (P < 0.001), systolic blood pressure (SBP) (P = 0.047), total cholesterol (T-C) (P < 0.001), and HDL-C (P < 0.001). Furthermore, a general linear model analysis revealed that interaction between age and MTHFR gene polymorphism was significantly associated with IMT, independently of age, SBP, T-C, and HDL-C in male subjects. However, age-gene interaction was not observed in female subjects. The findings of the present study confirm an association between MTHFR gene polymorphism and common carotid atherosclerosis in the Japanese population and further support the role of risk factor-gene interaction in common carotid atherosclerosis.
血浆同型半胱氨酸(Hcy)浓度已被证明受编码亚甲基四氢叶酸还原酶(MTHFR)的基因突变影响。尽管血浆Hcy与动脉粥样硬化性疾病相关,但关于MTHFR基因多态性与颈总动脉硬化病变之间的关联,已有相互矛盾的报道。我们在患有多种动脉粥样硬化危险因素的老年受试者中,研究了年龄-基因相互作用对颈动脉重塑的影响。我们通过超声检查评估了326例患者(平均年龄±标准差,73±12岁)的颈总动脉硬化病变,并研究了动脉粥样硬化已知危险因素之间的关系,包括MTHFR基因多态性及其与年龄和性别的相互作用。在326名研究对象中,136人具有MTHFR基因型CC,136人基因型CT,54人基因型TT。这三组在年龄、吸烟史、血压、血脂或尿酸等背景因素方面,或在动脉粥样硬化疾病的发病率方面没有差异。Spearman等级相关性分析显示,性别、年龄、布林克曼指数、收缩压、甘油三酯、高密度脂蛋白胆固醇(HDL-C)、尿酸与MTHFR基因多态性之间存在显著关系。以内膜-中膜复合体厚度(IMT)作为标准变量,以包括MTHFR基因多态性在内的危险因素作为解释变量进行多元回归分析表明,MTHFR基因多态性(P = 0.039)是IMT的一个显著独立解释变量,同时还有性别(男性)(P < 0.001)、年龄(P < 0.001)、收缩压(SBP)(P = 0.047)、总胆固醇(T-C)(P < 0.001)和HDL-C(P < 0.001)。此外,一般线性模型分析显示,年龄与MTHFR基因多态性之间的相互作用与男性受试者的IMT显著相关,独立于年龄、SBP、T-C和HDL-C。然而,在女性受试者中未观察到年龄-基因相互作用。本研究结果证实了日本人群中MTHFR基因多态性与颈总动脉粥样硬化之间的关联,并进一步支持了危险因素-基因相互作用在颈总动脉粥样硬化中的作用。