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A Dimension Reduction Approach for Modeling Multi-Locus Interaction in Case-Control Studies

机译:案例控制研究中多场所相互作用建模的降维方法

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摘要

Studying one locus or one single nucleotide polymorphism (SNP) at a time may not be sufficient to understand complex diseases because they are unlikely to result from the effect of only one SNP. Each SNP alone may have little or no effect on the risk of the disease, but together they may increase the risk substantially. Analyses focusing on individual SNPs ignore the possibility of interaction among SNPs. In this paper, we propose a parsimonious model to assess the joint effect of a group of SNPs in a case-control study. The model implements a data reduction strategy within a likelihood framework and uses a test to assess the statistical significance of the effect of the group of SNPs on the binary trait. The primary advantage of the proposed approach is that the dimension reduction technique produces a test statistic with degrees of freedom significantly lower than a multiple logistic regression with only main effects of the SNPs, and our parsimonious model can incorporate the possibility of interaction among the SNPs. Moreover, the proposed approach estimates the direction of association of each SNP with the disease and provides an estimate of the average effect of the group of SNPs positively and negatively associated with the disease in the given SNP set. We illustrate the proposed model on simulated and real data, and compare its performance with a few other existing approaches. Our proposed approach appeared to outperform the other approaches for independent SNPs in our simulation studies.
机译:一次研究一个基因座或一个单核苷酸多态性(SNP)可能不足以了解复杂的疾病,因为它们不可能仅由一种SNP的作用引起。单独使用每个SNP可能对疾病的风险影响很小或没有影响,但是它们一起可能会大大增加风险。专注于单个SNP的分析忽略了SNP之间相互作用的可能性。在本文中,我们提出了一种简约模型,用于评估病例对照研究中一组SNP的联合作用。该模型在可能性框架内实施了数据缩减策略,并使用检验来评估SNP组对二元性状影响的统计显着性。提出的方法的主要优点是,降维技术产生的测试统计量的自由度明显低于仅具有SNP的主要影响的多元逻辑回归,并且我们的简约模型可以考虑SNP之间相互作用的可能性。而且,所提出的方法估计了每个SNP与疾病的关联方向,并提供了在给定SNP集中与疾病正相关和负相关的SNP组的平均效应的估计。我们在模拟和真实数据上说明了所提出的模型,并将其性能与其他一些现有方法进行了比较。在我们的仿真研究中,我们提出的方法似乎胜过了其他针对独立SNP的方法。

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