Familial aggregation of diabetes and hypertension in a case-control study of colorectal neoplasia

被引:24
作者
Brauer, PM
McKeown-Eyssen, GE
Jazmaji, V
Logan, AG
Andrews, DF
Jenkins, D
Marcon, N
Saibil, F
Cohen, L
Stern, H
Baron, D
Greenberg, G
Diamandis, E
Kakis, G
Singer, W
Steiner, G
机构
[1] Univ Toronto, Dept Publ Hlth Sci, Toronto, ON, Canada
[2] Univ Toronto, Dept Nutr Sci, Toronto, ON, Canada
[3] Univ Toronto, Samuel Lunenfeld Res Inst, Toronto, ON, Canada
[4] Univ Toronto, Dept Med, Toronto, ON, Canada
[5] Univ Toronto, Dept Stat, Toronto, ON, Canada
[6] St Michaels Hosp, Dept Med, Toronto, ON M5B 1W8, Canada
[7] Wellesley Hosp, Dept Med, Toronto, ON, Canada
[8] Sunnybrook Med Ctr, Dept Med, Toronto, ON, Canada
[9] Womens Hlth Sci Ctr, Toronto, ON, Canada
[10] Ottawa Civic Hosp, Dept Surg, Ottawa, ON K1Y 4E9, Canada
[11] Univ Ottawa, Dept Surg, Ottawa, ON, Canada
[12] Mt Sinai Hosp, Dept Med, Toronto, ON M5G 1X5, Canada
[13] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[14] Mt Sinai Hosp, Dept Pathol & Lab Med, Toronto, ON M5G 1X5, Canada
[15] Toronto Hosp, Gen Div, Dept Med, Toronto, ON M5T 2S8, Canada
关键词
adenomatous polyps; case-control studies; colorectal neoplasms; diabetes mellitus; family; family health; hypertension; insulin resistance;
D O I
10.1093/aje/kwf112
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 [公共卫生与预防医学]; 120402 [社会医学与卫生事业管理];
摘要
Familial aggregation of diseases potentially associated with metabolic syndrome (diabetes mellitus, hypertension, and cardiovascular diseases) was assessed in a colonoscopy-based case-control study of colorectal neoplasia in Toronto and Ottawa, Canada, in 1993-1996. Each familial disease was analyzed by logistic regression using generalized estimating equations. Case probands had incident adenomatous polyps (n=172) or incident (n=25) or prevalent (n=132) colorectal cancer (CRC), while control probands (n=282) had a negative colonoscopy and no history of CRC or polyps. Significant effect modification was evident in the data, with the strongest positive associations between familial diabetes and colorectal neoplasia among older probands with symptoms (parents: odds ratio (OR)=2.4, 95% confidence interval (CI): 1.2, 4.8; siblings: OR=5.8, 95% CI: 2.6, 13.3). Familial hypertension was also associated with colorectal neoplasia among probands with symptoms (OR=1.7, 95% CI: 1.1, 2.6). In stratified analyses, familial diabetes, hypertension, and stroke were positively associated with adenomatous polyps in subgroups of probands who were older and/or had symptoms, while only familial diabetes was possibly associated with CRC. Associations in other proband groups may have been obscured by high cumulative incidence of parental CRC. Family studies are needed to understand the contribution of specific environmental and genetic factors in accounting for the disease aggregations.
引用
收藏
页码:702 / 713
页数:12
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