Association of Body Mass Index With Colorectal Cancer Risk by Genome-Wide Variants. (3rd September 2020)
- Record Type:
- Journal Article
- Title:
- Association of Body Mass Index With Colorectal Cancer Risk by Genome-Wide Variants. (3rd September 2020)
- Main Title:
- Association of Body Mass Index With Colorectal Cancer Risk by Genome-Wide Variants
- Authors:
- Campbell, Peter T
Lin, Yi
Bien, Stephanie A
Figueiredo, Jane C
Harrison, Tabitha A
Guinter, Mark A
Berndt, Sonja I
Brenner, Hermann
Chan, Andrew T
Chang-Claude, Jenny
Gallinger, Steven J
Gapstur, Susan M
Giles, Graham G
Giovannucci, Edward
Gruber, Stephen B
Gunter, Marc
Hoffmeister, Michael
Jacobs, Eric J
Jenkins, Mark A
Le Marchand, Loic
Li, Li
McLaughlin, John R
Murphy, Neil
Milne, Roger L
Newcomb, Polly A
Newton, Christina
Ogino, Shuji
Potter, John D
Rennert, Gad
Rennert, Hedy S
Robinson, Jennifer
Sakoda, Lori C
Slattery, Martha L
Song, Yiqing
White, Emily
Woods, Michael O
Casey, Graham
Hsu, Li
Peters, Ulrike
… (more) - Abstract:
- Abstract: Background: Body mass index (BMI) is a complex phenotype that may interact with genetic variants to influence colorectal cancer risk. Methods: We tested multiplicative statistical interactions between BMI (per 5 kg/m 2 ) and approximately 2.7 million single nucleotide polymorphisms with colorectal cancer risk among 14 059 colorectal cancer case (53.2% women) and 14 416 control (53.8% women) participants. All analyses were stratified by sex a priori . Statistical methods included 2-step (ie, Cocktail method) and single-step (ie, case-control logistic regression and a joint 2-degree of freedom test) procedures. All statistical tests were two-sided. Results: Each 5 kg/m 2 increase in BMI was associated with higher risks of colorectal cancer, less so for women (odds ratio [OR] = 1.14, 95% confidence intervals [CI] = 1.11 to 1.18; P = 9.75 × 10 –17 ) than for men (OR = 1.26, 95% CI = 1.20 to 1.32; P = 2.13 × 10 –24 ). The 2-step Cocktail method identified an interaction for women, but not men, between BMI and a SMAD7 intronic variant at 18q21.1 (rs4939827; P observed = .0009; P threshold = .005). A joint 2-degree of freedom test was consistent with this finding for women (joint P = 2.43 × 10 –10 ). Each 5 kg/m 2 increase in BMI was more strongly associated with colorectal cancer risk for women with the rs4939827- CC genotype (OR = 1.24, 95% CI = 1.16 to 1.32; P = 2.60 × 10 –10 ) than for women with the CT (OR = 1.14, 95% CI = 1.09 to 1.19; P = 1.04 × 10 –8 ) or TT (OR =Abstract: Background: Body mass index (BMI) is a complex phenotype that may interact with genetic variants to influence colorectal cancer risk. Methods: We tested multiplicative statistical interactions between BMI (per 5 kg/m 2 ) and approximately 2.7 million single nucleotide polymorphisms with colorectal cancer risk among 14 059 colorectal cancer case (53.2% women) and 14 416 control (53.8% women) participants. All analyses were stratified by sex a priori . Statistical methods included 2-step (ie, Cocktail method) and single-step (ie, case-control logistic regression and a joint 2-degree of freedom test) procedures. All statistical tests were two-sided. Results: Each 5 kg/m 2 increase in BMI was associated with higher risks of colorectal cancer, less so for women (odds ratio [OR] = 1.14, 95% confidence intervals [CI] = 1.11 to 1.18; P = 9.75 × 10 –17 ) than for men (OR = 1.26, 95% CI = 1.20 to 1.32; P = 2.13 × 10 –24 ). The 2-step Cocktail method identified an interaction for women, but not men, between BMI and a SMAD7 intronic variant at 18q21.1 (rs4939827; P observed = .0009; P threshold = .005). A joint 2-degree of freedom test was consistent with this finding for women (joint P = 2.43 × 10 –10 ). Each 5 kg/m 2 increase in BMI was more strongly associated with colorectal cancer risk for women with the rs4939827- CC genotype (OR = 1.24, 95% CI = 1.16 to 1.32; P = 2.60 × 10 –10 ) than for women with the CT (OR = 1.14, 95% CI = 1.09 to 1.19; P = 1.04 × 10 –8 ) or TT (OR = 1.07, 95% CI = 1.01 to 1.14; P = .02) genotypes. Conclusion: These results provide novel insights on a potential mechanism through which a SMAD7 variant, previously identified as a susceptibility locus for colorectal cancer, and BMI may influence colorectal cancer risk for women. … (more)
- Is Part Of:
- Journal of the National Cancer Institute. Volume 113:Number 1(2021)
- Journal:
- Journal of the National Cancer Institute
- Issue:
- Volume 113:Number 1(2021)
- Issue Display:
- Volume 113, Issue 1 (2021)
- Year:
- 2021
- Volume:
- 113
- Issue:
- 1
- Issue Sort Value:
- 2021-0113-0001-0000
- Page Start:
- 38
- Page End:
- 47
- Publication Date:
- 2020-09-03
- Subjects:
- Cancer -- Periodicals
Cancer -- Research -- Periodicals
616.994 - Journal URLs:
- https://jnci.oxfordjournals.org/ ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/jnci/djaa058 ↗
- Languages:
- English
- ISSNs:
- 0027-8874
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4830.000000
British Library DSC - BLDSS-3PM
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- 15768.xml