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Robust Tests for Additive Gene-Environment Interaction in Case-Control Studies Using Gene-Environment Independence

  • for the Ovarian Cancer Association Consortium
  • University of Michigan, Ann Arbor
  • University of Southern California
  • Rutgers - The State University of New Jersey, New Brunswick
  • Danish Cancer Society
  • Fred Hutchinson Cancer Research Center
  • University of Washington
  • German Cancer Research Center
  • University of Hamburg
  • Dartmouth College
  • University College London
  • Radboud University Nijmegen
  • University of Pittsburgh
  • Mayo Clinic Rochester, MN
  • University of Kansas
  • Brigham and Women’s Hospital
  • Harvard University
  • University of New South Wales
  • Garvan Institute of Medical Research
  • University of California at Irvine
  • University of Cambridge
  • University of Virginia
  • University of Copenhagen
  • Queensland Institute of Medical Research
  • University of Texas Health Science Center at Houston
  • Duke University
  • Yale University

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

There have been recent proposals advocating the use of additive gene-environment interaction instead of the widely used multiplicative scale, as a more relevant public health measure. Using gene-environment independence enhances statistical power for testing multiplicative interaction in case-control studies. However, under departure from this assumption, substantial bias in the estimates and inflated type I error in the corresponding tests can occur. In this paper, we extend the empirical Bayes (EB) approach previously developed for multiplicative interaction, which trades off between bias and efficiency in a data-adaptive way, to the additive scale. An EB estimator of the relative excess risk due to interaction is derived, and the corresponding Wald test is proposed with a general regression setting under a retrospective likelihood framework. We study the impact of gene-environment association on the resultant test with case-control data. Our simulation studies suggest that the EB approach uses the gene-environment independence assumption in a data-adaptive way and provides a gain in power compared with the standard logistic regression analysis and better control of type I error when compared with the analysis assuming gene-environment independence. We illustrate the methods with data from the Ovarian Cancer Association Consortium.

Original languageEnglish
Pages (from-to)366-377
Number of pages12
JournalAmerican Journal of Epidemiology
Volume187
Issue number2
DOIs
StatePublished - Feb 1 2018

Keywords

  • bias-variance tradeoff
  • effect modification
  • empirical Bayes estimation
  • genetic risk score
  • relative excess risk
  • shrinkage

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