Variation in the Association Between Colorectal Cancer Susceptibility Loci and Colorectal Polyps by Polyp Type

被引:13
|
作者
Burnett-Hartman, Andrea N. [1 ,2 ]
Newcomb, Polly A. [1 ,2 ]
Hutter, Carolyn M. [3 ]
Peters, Ulrike [1 ,2 ]
Passarelli, Michael N. [1 ,2 ]
Schwartz, Malaika R. [2 ]
Upton, Melissa P. [4 ]
Zhu, Lee-Ching [5 ]
Potter, John D. [1 ,2 ]
Makar, Karen W. [1 ,2 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Canc Prevent Program, Seattle, WA 98109 USA
[2] Univ Washington, Sch Publ Hlth, Dept Epidemiol, Seattle, WA 98195 USA
[3] NHGRI, NIH, Bethesda, MD 20892 USA
[4] Univ Washington, Sch Med, Dept Pathol, Seattle, WA 98195 USA
[5] Grp Hlth Cooperat Puget Sound, Seattle, WA USA
基金
美国国家卫生研究院;
关键词
adenoma; colorectal cancer; colorectal polyps; genome-wide association studies; serrated polyps; single-nucleotide polymorphisms; GENOME-WIDE ASSOCIATION; SERRATED POLYPS; HYPERPLASTIC POLYPS; ADENOMATOUS POLYPS; CIGARETTE-SMOKING; RISK-FACTORS; POLYMORPHISMS; METAANALYSIS; COLON; 8Q24;
D O I
10.1093/aje/kwu114
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
We conducted a case-control study of the association between subsets of colorectal polyps, including adenomas and serrated polyps, and single-nucleotide polymorphisms (SNPs) related to colorectal cancer through prior genome-wide association studies (GWAS). Participants were enrollees in the Group Health Cooperative (Seattle, Washington) aged 24-79 years who received a colonoscopy from 1998 to 2007, donated a buccal or blood sample, and completed a structured questionnaire. We performed genotyping of 13 colorectal cancer susceptibility SNPs. Polytomous logistic regression models were used to estimate odds ratios and 95% confidence intervals for associations between polyps and the colorectal cancer risk allele for each SNP under a log-additive model. Analyses included 781 controls, 489 cases with adenoma, 401 cases with serrated polyps, and 188 cases with both polyp types. The following SNPs were associated with advanced adenomas: rs10936599, rs10795668, rs16892766, and rs9929218 (P < 0.05). For nonadvanced adenomas and for serrated polyps overall, only rs961253 was statistically significant (P < 0.05). These associations were in the same directions as those in prior colorectal cancer GWAS. No SNP was significantly associated with hyperplastic polyps, and only rs6983267 was significantly associated with sessile serrated polyps, but this association was opposite of that found in colorectal cancer GWAS. Our results suggest that the association between colorectal cancer susceptibility SNPs and colorectal polyps varies by polyp type.
引用
收藏
页码:223 / 232
页数:10
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