TY - JOUR
T1 - Diabetes mellitus in relation to colorectal tumor molecular subtypes
T2 - A pooled analysis of more than 9000 cases
AU - Harlid, Sophia
AU - Van Guelpen, Bethany
AU - Qu, Conghui
AU - Gylling, Björn
AU - Aglago, Elom K.
AU - Amitay, Efrat L.
AU - Brenner, Hermann
AU - Buchanan, Daniel D.
AU - Campbell, Peter T.
AU - Cao, Yin
AU - Chan, Andrew T.
AU - Chang-Claude, Jenny
AU - Drew, David A.
AU - Figueiredo, Jane C.
AU - French, Amy J.
AU - Gallinger, Steven
AU - Giannakis, Marios
AU - Giles, Graham G.
AU - Gunter, Marc J.
AU - Hoffmeister, Michael
AU - Hsu, Li
AU - Jenkins, Mark A.
AU - Lin, Yi
AU - Moreno, Victor
AU - Murphy, Neil
AU - Newcomb, Polly A.
AU - Newton, Christina C.
AU - Nowak, Jonathan A.
AU - Obón-Santacana, Mireia
AU - Ogino, Shuji
AU - Potter, John D.
AU - Song, Mingyang
AU - Steinfelder, Robert S.
AU - Sun, Wei
AU - Thibodeau, Stephen N.
AU - Toland, Amanda E.
AU - Ugai, Tomotaka
AU - Um, Caroline Y.
AU - Woods, Michael O.
AU - Phipps, Amanda I.
AU - Harrison, Tabitha
AU - Peters, Ulrike
N1 - Publisher Copyright:
© 2022 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.
PY - 2022/8/1
Y1 - 2022/8/1
N2 - Diabetes is an established risk factor for colorectal cancer. However, colorectal cancer is a heterogeneous disease and it is not well understood whether diabetes is more strongly associated with some tumor molecular subtypes than others. A better understanding of the association between diabetes and colorectal cancer according to molecular subtypes could provide important insights into the biology of this association. We used data on lifestyle and clinical characteristics from the Colorectal Cancer Family Registry (CCFR) and the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO), including 9756 colorectal cancer cases (with tumor marker data) and 9985 controls, to evaluate associations between reported diabetes and risk of colorectal cancer according to molecular subtypes. Tumor markers included BRAF and KRAS mutations, microsatellite instability and CpG island methylator phenotype. In the multinomial logistic regression model, comparing colorectal cancer cases to cancer-free controls, diabetes was positively associated with colorectal cancer regardless of subtype. The highest OR estimate was found for BRAF-mutated colorectal cancer, n = 1086 (ORfully adj: 1.67, 95% confidence intervals [CI]: 1.36-2.05), with an attenuated association observed between diabetes and colorectal cancer without BRAF-mutations, n = 7959 (ORfully adj: 1.33, 95% CI: 1.19-1.48). In the case only analysis, BRAF-mutation was differentially associated with diabetes (Pdifference =.03). For the other markers, associations with diabetes were similar across tumor subtypes. In conclusion, our study confirms the established association between diabetes and colorectal cancer risk, and suggests that it particularly increases the risk of BRAF-mutated tumors.
AB - Diabetes is an established risk factor for colorectal cancer. However, colorectal cancer is a heterogeneous disease and it is not well understood whether diabetes is more strongly associated with some tumor molecular subtypes than others. A better understanding of the association between diabetes and colorectal cancer according to molecular subtypes could provide important insights into the biology of this association. We used data on lifestyle and clinical characteristics from the Colorectal Cancer Family Registry (CCFR) and the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO), including 9756 colorectal cancer cases (with tumor marker data) and 9985 controls, to evaluate associations between reported diabetes and risk of colorectal cancer according to molecular subtypes. Tumor markers included BRAF and KRAS mutations, microsatellite instability and CpG island methylator phenotype. In the multinomial logistic regression model, comparing colorectal cancer cases to cancer-free controls, diabetes was positively associated with colorectal cancer regardless of subtype. The highest OR estimate was found for BRAF-mutated colorectal cancer, n = 1086 (ORfully adj: 1.67, 95% confidence intervals [CI]: 1.36-2.05), with an attenuated association observed between diabetes and colorectal cancer without BRAF-mutations, n = 7959 (ORfully adj: 1.33, 95% CI: 1.19-1.48). In the case only analysis, BRAF-mutation was differentially associated with diabetes (Pdifference =.03). For the other markers, associations with diabetes were similar across tumor subtypes. In conclusion, our study confirms the established association between diabetes and colorectal cancer risk, and suggests that it particularly increases the risk of BRAF-mutated tumors.
KW - colorectal cancer
KW - diabetes
KW - subtype
UR - http://www.scopus.com/inward/record.url?scp=85129087573&partnerID=8YFLogxK
U2 - 10.1002/ijc.34015
DO - 10.1002/ijc.34015
M3 - Article
C2 - 35383926
AN - SCOPUS:85129087573
SN - 0020-7136
VL - 151
SP - 348
EP - 360
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 3
ER -