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dc.contributor.authorFigueiredo, Jane C.en_US
dc.contributor.authorHsu, Lien_US
dc.contributor.authorHutter, Carolyn M.en_US
dc.contributor.authorLin, Yien_US
dc.contributor.authorCampbell, Peter T.en_US
dc.contributor.authorBaron, John A.en_US
dc.contributor.authorBerndt, Sonja I.en_US
dc.contributor.authorJiao, Shuoen_US
dc.contributor.authorCasey, Grahamen_US
dc.contributor.authorFortini, Barbaraen_US
dc.contributor.authorChan, Andrew T.en_US
dc.contributor.authorCotterchio, Michelleen_US
dc.contributor.authorLemire, Mathieuen_US
dc.contributor.authorGallinger, Stevenen_US
dc.contributor.authorHarrison, Tabitha A.en_US
dc.contributor.authorLe Marchand, Loicen_US
dc.contributor.authorNewcomb, Polly A.en_US
dc.contributor.authorSlattery, Martha L.en_US
dc.contributor.authorCaan, Bette J.en_US
dc.contributor.authorCarlson, Christopher S.en_US
dc.contributor.authorZanke, Brent W.en_US
dc.contributor.authorRosse, Stephanie A.en_US
dc.contributor.authorBrenner, Hermannen_US
dc.contributor.authorGiovannucci, Edward L.en_US
dc.contributor.authorWu, Kanaen_US
dc.contributor.authorChang-Claude, Jennyen_US
dc.contributor.authorChanock, Stephen J.en_US
dc.contributor.authorCurtis, Keith R.en_US
dc.contributor.authorDuggan, Daviden_US
dc.contributor.authorGong, Jianen_US
dc.contributor.authorHaile, Robert W.en_US
dc.contributor.authorHayes, Richard B.en_US
dc.contributor.authorHoffmeister, Michaelen_US
dc.contributor.authorHopper, John L.en_US
dc.contributor.authorJenkins, Mark A.en_US
dc.contributor.authorKolonel, Laurence N.en_US
dc.contributor.authorQu, Conghuien_US
dc.contributor.authorRudolph, Anjaen_US
dc.contributor.authorSchoen, Robert E.en_US
dc.contributor.authorSchumacher, Fredrick R.en_US
dc.contributor.authorSeminara, Danielaen_US
dc.contributor.authorStelling, Deanna L.en_US
dc.contributor.authorThibodeau, Stephen N.en_US
dc.contributor.authorThornquist, Marken_US
dc.contributor.authorWarnick, Greg S.en_US
dc.contributor.authorHenderson, Brian E.en_US
dc.contributor.authorUlrich, Cornelia M.en_US
dc.contributor.authorGauderman, W. Jamesen_US
dc.contributor.authorPotter, John D.en_US
dc.contributor.authorWhite, Emilyen_US
dc.contributor.authorPeters, Ulrikeen_US
dc.date.accessioned2014-05-06T16:16:14Z
dc.date.issued2014en_US
dc.identifier.citationFigueiredo, J. C., L. Hsu, C. M. Hutter, Y. Lin, P. T. Campbell, J. A. Baron, S. I. Berndt, et al. 2014. “Genome-Wide Diet-Gene Interaction Analyses for Risk of Colorectal Cancer.” PLoS Genetics 10 (4): e1004228. doi:10.1371/journal.pgen.1004228. http://dx.doi.org/10.1371/journal.pgen.1004228.en
dc.identifier.issn1553-7390en
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:12152846
dc.description.abstractDietary factors, including meat, fruits, vegetables and fiber, are associated with colorectal cancer; however, there is limited information as to whether these dietary factors interact with genetic variants to modify risk of colorectal cancer. We tested interactions between these dietary factors and approximately 2.7 million genetic variants for colorectal cancer risk among 9,287 cases and 9,117 controls from ten studies. We used logistic regression to investigate multiplicative gene-diet interactions, as well as our recently developed Cocktail method that involves a screening step based on marginal associations and gene-diet correlations and a testing step for multiplicative interactions, while correcting for multiple testing using weighted hypothesis testing. Per quartile increment in the intake of red and processed meat were associated with statistically significant increased risks of colorectal cancer and vegetable, fruit and fiber intake with lower risks. From the case-control analysis, we detected a significant interaction between rs4143094 (10p14/near GATA3) and processed meat consumption (OR = 1.17; p = 8.7E-09), which was consistently observed across studies (p heterogeneity = 0.78). The risk of colorectal cancer associated with processed meat was increased among individuals with the rs4143094-TG and -TT genotypes (OR = 1.20 and OR = 1.39, respectively) and null among those with the GG genotype (OR = 1.03). Our results identify a novel gene-diet interaction with processed meat for colorectal cancer, highlighting that diet may modify the effect of genetic variants on disease risk, which may have important implications for prevention.en
dc.language.isoen_USen
dc.publisherPublic Library of Scienceen
dc.relation.isversionofdoi:10.1371/journal.pgen.1004228en
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990510/pdf/en
dash.licenseLAAen_US
dc.subjectMedicine and Health Sciencesen
dc.subjectEpidemiologyen
dc.subjectGastroenterology and Hepatologyen
dc.titleGenome-Wide Diet-Gene Interaction Analyses for Risk of Colorectal Canceren
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden
dc.relation.journalPLoS Geneticsen
dash.depositing.authorChan, Andrew T.en_US
dc.date.available2014-05-06T16:16:14Z
dc.identifier.doi10.1371/journal.pgen.1004228*
dash.authorsorderedfalse
dash.contributor.affiliatedWu, Kana
dash.contributor.affiliatedChan, Andrew


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