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Testing Departure from Additivity in Tukey’s Model using Shrinkage: Application to a Longitudinal Setting

机译:使用收缩测试Tukey模型中可加性的偏离:在纵向环境中的应用

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摘要

While there has been extensive research developing gene-environment interaction (GEI) methods in case-control studies, little attention has been given to sparse and efficient modeling of GEI in longitudinal studies. In a two-way table for GEI with rows and columns as categorical variables, a conventional saturated interaction model involves estimation of a specific parameter for each cell, with constraints ensuring identifiability. The estimates are unbiased but are potentially inefficient because the number of parameters to be estimated can grow quickly with increasing categories of row/column factors. On the other hand, Tukey’s one degree of freedom (df) model for non-additivity treats the interaction term as a scaled product of row and column main effects. Due to the parsimonious form of interaction, the interaction estimate leads to enhanced efficiency and the corresponding test could lead to increased power. Unfortunately, Tukey’s model gives biased estimates and low power if the model is misspecified. When screening multiple GEIs where each genetic and environmental marker may exhibit a distinct interaction pattern, a robust estimator for interaction is important for GEI detection. We propose a shrinkage estimator for interaction effects that combines estimates from both Tukey’s and saturated interaction models and use the corresponding Wald test for testing interaction in a longitudinal setting. The proposed estimator is robust to misspecification of interaction structure. We illustrate the proposed methods using two longitudinal studies — the Normative Aging Study and the Multi-Ethnic Study of Atherosclerosis.
机译:尽管有大量研究在病例对照研究中开发基因-环境相互作用(GEI)方法,但在纵向研究中很少关注GEI的稀疏高效模型。在以行和列为分类变量的GEI双向表中,常规的饱和交互模型涉及估计每个单元格的特定参数,并具有确保可识别性的约束。估计是无偏的,但可能效率不高,因为要估计的参数数量会随着行/列因子类别的增加而快速增长。另一方面,Tukey的非可加性单自由度(df)模型将交互作用项视为行和列主效应的缩放乘积。由于交互的简约形式,交互估计会提高效率,而相应的测试可能会导致功率增加。不幸的是,如果模型指定不正确,Tukey的模型会给出有偏差的估计,并且功耗较低。当筛选多个GEI时,每个遗传和环境标记都可能表现出不同的相互作用模式,因此,一种可靠的相互作用估计器对于GEI检测很重要。我们为交互作用提出了一种收缩估计器,该方法将来自Tukey和饱和交互模型的估计值结合在一起,并使用相应的Wald检验在纵向环境下测试交互作用。所提出的估计器对于交互结构的错误指定具有鲁棒性。我们使用两项纵向研究来说明所提议的方法-规范性衰老研究和动脉粥样硬化的多民族研究。

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