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@ARTICLE{Liu:132495,
author = {G. Liu and B. Mukherjee and S. Lee and A. W. Lee and A. H.
Wu and E. V. Bandera and A. Jensen and M. A. Rossing and K.
B. Moysich and J. Chang-Claude$^*$ and J. A. Doherty and A.
Gentry-Maharaj and L. Kiemeney and S. A. Gayther and F.
Modugno and L. Massuger and E. L. Goode and B. L. Fridley
and K. L. Terry and D. W. Cramer and S. J. Ramus and H.
Anton-Culver and A. Ziogas and J. P. Tyrer and J. M.
Schildkraut and S. K. Kjaer and P. M. Webb and R. B. Ness
and U. Menon and A. Berchuck and P. D. Pharoah and H. Risch
and C. L. Pearce},
collaboration = {O. C. A. Consortium},
title = {{R}obust {T}ests for {A}dditive {G}ene-{E}nvironment
{I}nteraction in {C}ase-{C}ontrol {S}tudies {U}sing
{G}ene-{E}nvironment {I}ndependence.},
journal = {American journal of epidemiology},
volume = {187},
number = {2},
issn = {1476-6256},
address = {Oxford},
publisher = {Oxford Univ. Press},
reportid = {DKFZ-2018-00182},
pages = {366 - 377},
year = {2018},
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.},
cin = {C020},
ddc = {610},
cid = {I:(DE-He78)C020-20160331},
pnm = {313 - Cancer risk factors and prevention (POF3-313)},
pid = {G:(DE-HGF)POF3-313},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:28633381},
doi = {10.1093/aje/kwx243},
url = {https://inrepo02.dkfz.de/record/132495},
}