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Evaluation of association studies and meta-analyses of MTHFR gene polymorphisms in colorectal cancer

机译:MTHFR基因多态性与结直肠癌的关联研究和荟萃分析的评价

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There is a discrepancy between the results of 89 original studies and 15 meta-analyses investigating the association of MTHFR rs1801133 and rs1801131 polymorphisms with colorectal cancer (CRC) risk. We examined this hypothesis through meta-analyses of both loci and their diplotypes as well as evaluation of previous meta-analyses. The present meta-analysis showed that rs1801133 and rs1801131 might be CRC susceptibility variants in Americans and Australians and rs1801133 in Brazilians and Japanese. A strong linkage disequilibrium was observed between both loci and their diplotypes were associated with CRC risk. Evaluation of 15 meta-analyses showed a high discrepancy among their findings, mainly caused by population stratification of original studies and data analysis strategies in meta-analysis. Population stratification was more dominant in the studies from Australia, America and Brazil leading to false positive or negative results. In conclusion, these loci alone might modify the development of CRC in some ethnicities.
机译:89项原始研究的结果与15项荟萃分析之间的差异,该荟萃分析调查了MTHFR rs1801133和rs1801131多态性与结直肠癌(CRC)风险的关系。我们通过基因座及其双倍型的荟萃分析以及对先前荟萃分析的评估,检验了这一假设。目前的荟萃分析显示,rs1801133和rs1801131可能是美国人和澳大利亚人的CRC敏感性变异体,而rs1801133是巴西人和日本人的CRC敏感性变异体。在两个基因座之间均观察到强烈的连锁不平衡,并且其双倍型与CRC风险有关。对15项荟萃分析的评估显示出他们的发现之间存在高度差异,这主要是由于原始研究的人群分层和荟萃分析中的数据分析策略所致。在澳大利亚,美国和巴西进行的研究中,人口分层更为主导,从而导致假阳性或阴性结果。总之,仅这些基因座可能会改变某些种族的CRC发展。

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