首页> 外文期刊>Journal of Cardiovascular Disease Research >Genetic interactions between MTHFR (C677T), methionine synthase (A2756G, C2758G) variants with vitamin B12 and folic acid determine susceptibility to premature coronary artery disease in Indian population
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Genetic interactions between MTHFR (C677T), methionine synthase (A2756G, C2758G) variants with vitamin B12 and folic acid determine susceptibility to premature coronary artery disease in Indian population

机译:MTHFR(C677T),蛋氨酸合酶(A2756G,C275​​8G)变体与维生素B12和叶酸之间的遗传相互作用决定了印度人群中早发冠心病的易感性

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Background: Researchers have determined that Indians face a higher risk of heart disease, despite the fact that nearly half of them are vegetarians and lack many of the other traditional risk factors. In the below-30 age group, coronary artery disease mortality among Indians is three-fold higher than in the whites in United Kingdom and ten-fold higher than the Chinese in Singapore. High levels of homocysteine have been widely linked to the early onset of heart diseases in other populations, although a definite proof among Indians is lacking, which needs to be investigated by way of screening for factors responsible for high homocysteine levels. Objective: To screen for genetic factors responsible for hyperhomocysteinemia and the risk for premature coronary artery disease. Materials and Methods: A total of 100 individuals with proven premature coronary artery disease and 200 age-and-sex matched controls were screened for polymorphisms in Methylenetetrahydrofolate reductase (MTHFR) (C677T) Methionine synthase (MS) genes (A2756G, C2758G), and the B12 and Folate levels were estimated. Results: Results from the mutational analysis revealed that in the study group, seven individuals had a polymorphism for the C677T allele in the MTHFR gene (one homozygous and six heterozygous) (Fischer’s Exact test P > 0.046) (OR: 0.2711 95% CI 0.0774 to 0.9491). Six were heterozygous for the A2756G polymorphism in the MS gene (Fischer’s Exact test P > 0.0012). None showed a polymorphism at the C2758G allele in the MS gene. Four controls showed heterozygosity for the C677T polymorphism and none for the MS gene. The B12 and Folate levels were significantly lower in the study group as compared to the controls. Conclusions: It is important to know which factors determine the total homocysteine concentrations. In the general population, the most important modifiable determinants of tHcy are folate intake and coffee consumption. Smoking and alcohol consumption are also associated with the total homocysteine concentrations, but more research is necessary to elucidate whether these relations are not originating from residual confounding due to other lifestyle factors.
机译:背景:研究人员已经确定,尽管印度人中将近一半是素食者,并且缺乏许多其他传统的危险因素,但他们面临心脏病的风险较高。在30岁以下的年龄组中,印度人的冠状动脉疾病死亡率比英国的白人高三倍,比新加坡的中国人高十倍。高水平的同型半胱氨酸已与其他人群的心脏病的早期发作广泛相关,尽管印度人缺乏明确的证据,需要通过筛选导致高同型半胱氨酸水平的因素进行调查。目的:筛选引起高同型半胱氨酸血症的遗传因素和早发冠心病的风险。材料和方法:筛选了100名已证明患有早发冠状动脉疾病的个体和200名年龄和性别相匹配的对照,以研究亚甲基四氢叶酸还原酶(MTHFR)(C677T)蛋氨酸合酶(MS)基因(A2756G,C275​​8G)的多态性,以及估计了B12和叶酸水平。结果:突变分析的结果显示,在研究组中,有七个个体的MTHFR基因C677T等位基因具有多态性(一个纯合子和六个杂合子)(Fischer精确检验P> 0.046)(或:0.2711 95%CI 0.0774)至0.9491)。六个是MS基因中A2756G多态性的杂合子(Fischer精确检验P> 0.0012)。在MS基因的C2758G等位基因上没有显示出多态性。四个对照显示C677T多态性为杂合性,而MS基因则无。与对照组相比,研究组的B12和叶酸水平显着降低。结论:重要的是要知道哪些因素决定总同型半胱氨酸的浓度。在一般人群中,tHcy最重要的可修改决定因素是叶酸摄入量和咖啡摄入量。吸烟和饮酒也与同型半胱氨酸的总浓度有关,但是有必要进行更多的研究来阐明这些关系是否不是由于其他生活方式因素而导致的残余混杂。

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