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Association of three-gene interaction among MTHFR, ALOX5AP and NOTCH3 with thrombotic stroke: a multicenter case-control study.

机译:MTHFR,ALOX5AP和NOTCH3三基因相互作用与血栓性卒中的关联:多中心病例对照研究。

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摘要

Stroke is a common complex trait and does not follow Mendelian pattern of inheritance. Gene-gene or gene-environment interactions may be responsible for the complex trait. How the interactions contribute to stroke is still under research. This study aimed to explore the association between gene-gene interactions and stroke in Chinese in a large case-control study. Nearly 4,000 participants were recruited from seven clinical centers. Eight variants in five candidate genes were examined for stroke risk. Gene-gene interactions were explored by using Generalized Multifactor Dimensionality Reduction (GMDR). A significant gene-gene interaction was found by GMDR. The best model including MTHFR C677T, ALOX5AP T2354A and NOTCH3 C381T scored 10 for Cross-Validation Consistency and 9 for Sign Test (P = 0.0107). The individuals with combination of MTHFR 677TT, ALOX5AP 2354AA and NOTCH3 381TT/TC had a significantly higher risk of thrombotic stroke (OR 3.165, 95% CI 1.461-6.858, P = 0.003). Our results show that combination of these alleles conferred higher risk for stroke than single risk allele. The gene-gene interaction may serve as a novel area for stroke research. The three-locus combination may change the susceptibility of particular subjects to the disease.
机译:中风是一个常见的复杂特征,并不遵循孟德尔的遗传模式。基因-基因或基因-环境的相互作用可能是造成复杂性状的原因。相互作用如何导致中风仍在研究中。这项研究旨在探讨一项大型病例对照研究中的基因-基因相互作用与中风之间的关联。从七个临床中心招募了近4,000名参与者。检查了五个候选基因中的八个变体的中风风险。通过使用广义多因素降维(GMDR)探索了基因与基因的相互作用。 GMDR发现了显着的基因-基因相互作用。包括MTHFR C677T,ALOX5AP T2354A和NOTCH3 C381T在内的最佳模型的交叉验证一致性得分为10,而符号测试得分为9(P = 0.0107)。结合使用MTHFR 677TT,ALOX5AP 2354AA和NOTCH3 381TT / TC的个体血栓性中风的风险显着更高(OR 3.165,95%CI 1.461-6.858,P = 0.003)。我们的结果表明,这些等位基因的组合比单风险等位基因具有更高的中风风险。基因与基因的相互作用可以作为中风研究的新领域。三位点组合可能会改变特定对象对疾病的敏感性。

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