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Three Genetic Polymorphisms of Homocysteine-Metabolizing Enzymes and Risk of Coronary Heart Disease: Appraisal of a Recent Meta-Analysis

机译:同型半胱氨酸代谢酶的三种遗传多态性和冠心病的风险:最近的荟萃分析的评估。

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We read with great interest the recent article entitled ‘‘Three Genetic Polymorphisms of HomocysteineMetabolizing Enzymes and Risk of Coronary Heart Disease: A Meta-Analysis Based on 23 Case-Control Studies’’ by Chen et al. (2011). To date, several studies have focused on the role of homocysteine-metabolizing enzymes polymorphisms in coronary heart disease (CHD) risk, however, the results of those studies remain inconclusive and ambiguous. Chen et al. (2011) conducted a meta-analysis to examine the associations between three genetic polymorphisms of genes encoding homocysteine-metabolizing enzymes (methionine synthase [MTR] A2756G, methionine synthase reductase [MTRR] A66G, and N 5 , N 10 - methylenetetrahydrofolate reductase [MTHFR] A1298C) and susceptibility to CHD. The results of this meta-analysis suggest that MTR A2756G polymorphism is associated with an increased risk of CHD for Europeans, whereas, for MTRR A66G and MTHFR A1298C, no obvious associations were found. It is an interesting study. Nonetheless, several issues related to the article seem worthy of comment.
机译:我们非常感兴趣地阅读了Chen等人最近发表的题为“同型半胱氨酸代谢酶的三种遗传多态性与冠心病风险:基于23个病例对照研究的荟萃分析”的文章。 (2011)。迄今为止,几项研究集中于高半胱氨酸代谢酶多态性在冠心病(CHD)风险中的作用,但是,这些研究的结果仍未定论和模棱两可。 Chen等。 (2011)进行了荟萃分析,以研究编码同型半胱氨酸代谢酶的基因的三个遗传多态性(蛋氨酸合酶[MTR] A2756G,蛋氨酸合酶还原酶[MTRR] A66G和N 5,N 10-亚甲基四氢叶酸还原酶[MTHFR A1298C)和对CHD的易感性。荟萃分析的结果表明,MTR A2756G基因多态性与欧洲人冠心病风险增加相关,而对于MTRR A66G和MTHFR A1298C,未发现明显关联。这是一个有趣的研究。尽管如此,与本文相关的一些问题似乎值得评论。

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