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An Analytic Approach Using Candidate Gene Selection and Logic Forest to Identify Gene by Environment Interactions (G × E) for Systemic Lupus Erythematosus in African Americans

机译:利用候选基因选择和逻辑森林鉴定基因的分析方法鉴定基因的环境相互作用(G×e)非洲裔美国人类红斑狼疮

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摘要

Development and progression of many human diseases, such as systemic lupus erythematosus (SLE), are hypothesized to result from interactions between genetic and environmental factors. Current approaches to identify and evaluate interactions are limited, most often focusing on main effects and two-way interactions. While higher order interactions associated with disease are documented, they are difficult to detect since expanding the search space to all possible interactions of p predictors means evaluating 2p − 1 terms. For example, data with 150 candidate predictors requires considering over 1045 main effects and interactions. In this study, we present an analytical approach involving selection of candidate single nucleotide polymorphisms (SNPs) and environmental and/or clinical factors and use of Logic Forest to identify predictors of disease, including higher order interactions, followed by confirmation of the association between those predictors and interactions identified with disease outcome using logistic regression. We applied this approach to a study investigating whether smoking and/or secondhand smoke exposure interacts with candidate SNPs resulting in elevated risk of SLE. The approach identified both genetic and environmental risk factors, with evidence suggesting potential interactions between exposure to secondhand smoke as a child and genetic variation in the ITGAM gene associated with increased risk of SLE.
机译:许多人类疾病,如系统性红斑狼疮(SLE)的发展和进展中,假设从遗传和环境因素之间的相互作用引起的。目前的方法来识别和评估的交互限制,通常集中在主效应和双向互动。虽然与疾病相关的高阶交互记录,他们是困难的,因为搜索空间扩展到的对预测方法的所有可能的相互作用评估2P检测 - 1项。例如,对于150个候选预测值数据需要考虑超过1045主效应和相互作用。在这项研究中,我们提出了一种分析方法涉及候选的单核苷酸多态性(SNP)和环境和/或临床因素和使用逻辑森林来识别疾病的预测,包括较高阶的相互作用的选择,随后的那些之间的关联的确认预测和相互作用确定使用logistic回归疾病的结果。我们把这种方法用于研究调查是否吸烟和/或二手导致SLE的高风险与种候选SNP烟雾暴露交互。这种方法确定的遗传和环境危险因素,有证据表明,二手烟是与SLE的风险增加相关的基因ITGAM小时候和遗传变异曝光之间潜在的相互作用。

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