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GWAS Study

Genome-wide diet-gene interaction analyses for risk of colorectal cancer.

Figueiredo JC, Hsu L, Hutter CM et al.

24743840 PubMed ID
GWAS Study Type
18404 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

FJ
Figueiredo JC
HL
Hsu L
HC
Hutter CM
LY
Lin Y
CP
Campbell PT
BJ
Baron JA
BS
Berndt SI
JS
Jiao S
CG
Casey G
FB
Fortini B
CA
Chan AT
CM
Cotterchio M
LM
Lemire M
GS
Gallinger S
HT
Harrison TA
LM
Le Marchand L
NP
Newcomb PA
SM
Slattery ML
CB
Caan BJ
CC
Carlson CS
ZB
Zanke BW
RS
Rosse SA
BH
Brenner H
GE
Giovannucci EL
WK
Wu K
CJ
Chang-Claude J
CS
Chanock SJ
CK
Curtis KR
DD
Duggan D
GJ
Gong J
HR
Haile RW
HR
Hayes RB
HM
Hoffmeister M
HJ
Hopper JL
JM
Jenkins MA
KL
Kolonel LN
QC
Qu C
RA
Rudolph A
SR
Schoen RE
SF
Schumacher FR
SD
Seminara D
SD
Stelling DL
TS
Thibodeau SN
TM
Thornquist M
WG
Warnick GS
HB
Henderson BE
UC
Ulrich CM
GW
Gauderman WJ
PJ
Potter JD
WE
White E
PU
Peters U
Chapter II

Abstract

Summary of the research findings

Dietary 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.

9,287 European ancestry cases, 9,117 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

18404
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.S., Australia, Canada, Germany
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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