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An application of conditional logistic regression and multifactor dimensionality reduction for detecting gene-gene Interactions on risk of myocardial infarction: The importance of model validation

机译:条件对数回归和多维度降维在检测基因-基因相互作用对心肌梗死风险中的应用:模型验证的重要性

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Background To examine interactions among the angiotensin converting enzyme ( ACE ) insertion/deletion, plasminogen activator inhibitor-1 ( PAI-1 ) 4G/5G , and tissue plasminogen activator ( t-PA ) insertion/deletion gene polymorphisms on risk of myocardial infarction using data from 343 matched case-control pairs from the Physicians Health Study. We examined the data using both conditional logistic regression and the multifactor dimensionality reduction (MDR) method. One advantage of the MDR method is that it provides an internal prediction error for validation. We summarize our use of this internal prediction error for model validation. Results The overall results for the two methods were consistent, with both suggesting an interaction between the ACE I/D and PAI-1 4G/5G polymorphisms. However, using ten-fold cross validation, the 46% prediction error for the final MDR model was not significantly lower than that expected by chance. Conclusions The significant interaction initially observed does not validate and may represent a type I error. As data-driven analytic methods continue to be developed and used to examine complex genetic interactions, it will become increasingly important to stress model validation in order to ensure that significant effects represent true relationships rather than chance findings.
机译:背景研究使用血管紧张素转换酶(ACE)插入/缺失,纤溶酶原激活物抑制剂-1(PAI-1)4G / 5G和组织纤溶酶原激活物(t-PA)插入/缺失基因多态性之间的相互作用,通过使用来自Physicians Health Study的343个匹配的病例对照对的数据。我们使用条件逻辑回归和多因素降维(MDR)方法检查了数据。 MDR方法的一个优点是,它为验证提供了内部预测误差。我们总结了这种内部预测误差在模型验证中的使用。结果两种方法的总体结果是一致的,均表明ACE I / D与PAI-1 4G / 5G多态性之间存在相互作用。但是,使用十倍交叉验证,最终MDR模型的46%预测误差不会显着低于偶然预期的误差。结论最初观察到的重大交互作用未得到验证,可能代表I型错误。随着数据驱动的分析方法的不断发展并用于检查复杂的遗传相互作用,对应力模型进行验证以确保重要的影响代表真实的关系而不是偶然的发现将变得越来越重要。

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