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@ARTICLE{Kim:141809,
author = {S. Kim and M. Wang and J. P. Tyrer and A. Jensen and A.
Wiensch and G. Liu and A. W. Lee and R. B. Ness and M.
Salvatore and S. S. Tworoger and A. S. Whittemore and H.
Anton-Culver and W. Sieh and S. H. Olson and A. Berchuck and
E. L. Goode and M. T. Goodman and J. A. Doherty and G.
Chenevix-Trench and M. A. Rossing and P. M. Webb and G. G.
Giles and K. L. Terry and A. Ziogas and R.
Turzanski-Fortner$^*$ and U. Menon and S. A. Gayther and A.
H. Wu and H. Song and A. Brooks-Wilson and E. V. Bandera and
L. S. Cook and D. W. Cramer and R. L. Milne and S. J. Winham
and S. K. Kjaer and F. Modugno and P. J. Thompson and J.
Chang-Claude$^*$ and H. R. Harris and J. M. Schildkraut and
N. D. Le and N. Wentzensen and B. Trabert and E. Høgdall
and D. Huntsman and M. C. Pike and P. D. P. Pharoah and C.
L. Pearce and B. Mukherjee},
title = {{A} {C}omprehensive {G}ene-{E}nvironment {I}nteraction
{A}nalysis in {O}varian {C}ancer using {G}enome-wide
{S}ignificant {C}ommon {V}ariants.},
journal = {International journal of cancer},
volume = {144},
number = {9},
issn = {0020-7136},
address = {Bognor Regis},
publisher = {Wiley-Liss},
reportid = {DKFZ-2018-02077},
pages = {2192-2205},
year = {2019},
abstract = {As a follow-up to genome-wide association analysis of
common variants associated with ovarian carcinoma (cancer),
this study considers seven well-known ovarian cancer risk
factors and their interactions with 28 genome-wide
significant common genetic variants. The interaction
analyses were based on data from 9,971 ovarian cancer cases
and 15,566 controls from 17 case-control studies. Likelihood
ratio and Wald tests for multiplicative interaction and for
relative excess risk due to additive interaction were used.
The top multiplicative interaction was noted between oral
contraceptive pill (OCP) use (ever vs never) and rs13255292
(P-value = 3.48 x 10-4 ). Among women with the TT genotype
for this variant, the odds ratio for OCP use was 0.53
$(95\%$ CI=0.46-0.60) compared to 0.71 $(95\%CI=0.66-0.77)$
for women with the CC genotype. When stratified by duration
of OCP use, women with 1-5 years of OCP use exhibited
differential protective benefit across genotypes. However,
no interaction on either the multiplicative or additive
scale was found to be statistically significant after
multiple testing correction. The results suggest that OCP
use may offer increased benefit for women who are carriers
of the T allele in rs13255292. On the other hand, for women
carrying the C allele in this variant, longer (5+ years) use
of OCP may reduce the impact of carrying the risk allele of
this SNP. Replication of this finding is needed. The study
presents a comprehensive analytic framework for conducting
gene-environment analysis in ovarian cancer. This article is
protected by copyright. All rights reserved.},
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:30499236},
doi = {10.1002/ijc.32029},
url = {https://inrepo02.dkfz.de/record/141809},
}