Type 2 diabetes risk variants and colorectal cancer risk: the Multiethnic Cohort and PAGE studies

被引:36
|
作者
Cheng, Iona [1 ]
Caberto, Christian P. [1 ]
Lum-Jones, Annette [1 ]
Seifried, Ann [1 ]
Wilkens, Lynne R. [1 ]
Schumacher, Fredrick R. [2 ]
Monroe, Kristine R. [2 ]
Lim, Unhee [1 ]
Tiirikainen, Maarit [1 ]
Kolonel, Laurence N. [1 ]
Henderson, Brian E. [2 ]
Stram, Daniel O. [2 ]
Haiman, Christopher A. [2 ]
Le Marchand, Loic [1 ]
机构
[1] Univ Hawaii, Univ Hawaii Canc Ctr, Program Epidemiol, Honolulu, HI 96817 USA
[2] Univ So Calif, Keck Sch Med, Norris Comprehens Canc Ctr, Dept Prevent Med, Los Angeles, CA 90033 USA
关键词
GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY LOCI; COMMON VARIANTS; PROSTATE-CANCER; COLON-CANCER; INSULIN; POPULATIONS; MELLITUS; GENES; HYPERINSULINEMIA;
D O I
10.1136/gut.2011.237727
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Diabetes has been positively associated with the risk of colorectal cancer. This study investigated whether recently established risk variants for diabetes also have effects on colorectal cancer. Methods 19 single nucleotide repeats (SNPs) associated with type 2 diabetes in genome-wide association studies were tested in a case-control study of 2011 colorectal cancer cases and 6049 controls nested in the Multiethnic Cohort study as part of the Population Architecture using Genomics and Epidemiology (PAGE) initiative. ORs and 95% CIs were estimated by unconditional logistic regression to evaluate the association between SNPs and colorectal cancer risk, adjusting for age, sex and race/ethnicity. Permutation testing was conducted to correct for multiple hypothesis testing. Results Four type 2 diabetes SNPs were associated with colorectal cancer risk: rs7578597 (THADA), rs864745 (JAZF1), rs5219 (KCNJ11) and rs7961581 (TSPAN8, LGR5). The strongest association was for the rs7578597 (THADA) Thr1187Ala missense polymorphism (P(trend)=0.004 adjusted for multiple testing), with the high risk allele for colorectal cancer being the low risk allele for diabetes. Similar patterns of associations were seen with further adjustment for diabetes status and body mass index. The association of diabetes status with colorectal cancer risk was somewhat weakened after adjustment for these SNPs. Conclusion The findings suggest that diabetes risk variants also influence colorectal cancer susceptibility, possibly through mechanisms different from those for diabetes.
引用
收藏
页码:1703 / 1711
页数:9
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