| Literature DB >> 28633381 |
Gang Liu1, Bhramar Mukherjee1, Seunggeun Lee1, Alice W Lee2, Anna H Wu2, Elisa V Bandera3, Allan Jensen4, Mary Anne Rossing5,6, Kirsten B Moysich7, Jenny Chang-Claude8,9, Jennifer A Doherty10, Aleksandra Gentry-Maharaj11, Lambertus Kiemeney12, Simon A Gayther2, Francesmary Modugno13,14,15, Leon Massuger16, Ellen L Goode17, Brooke L Fridley18, Kathryn L Terry19,20, Daniel W Cramer19,20, Susan J Ramus21,22, Hoda Anton-Culver23, Argyrios Ziogas23, Jonathan P Tyrer24, Joellen M Schildkraut25, Susanne K Kjaer4,26, Penelope M Webb27, Roberta B Ness28, Usha Menon11, Andrew Berchuck29, Paul D Pharoah24,30, Harvey Risch31, Celeste Leigh Pearce2,32.
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.Entities:
Keywords: bias-variance tradeoff; effect modification; empirical Bayes estimation; genetic risk score; relative excess risk; shrinkage
Mesh:
Year: 2018 PMID: 28633381 PMCID: PMC5860584 DOI: 10.1093/aje/kwx243
Source DB: PubMed Journal: Am J Epidemiol ISSN: 0002-9262 Impact factor: 4.897