TY - JOUR
T1 - Waist Circumference, a Body Shape Index, and Molecular Subtypes of Colorectal Cancer
T2 - A Pooled Analysis of Four Cohort Studies
AU - Chalitsios, Christos V.
AU - Markozannes, Georgios
AU - Papagiannopoulos, Christos
AU - Aglago, Elom K.
AU - Berndt, Sonja I.
AU - Buchanan, Daniel D.
AU - Campbell, Peter T.
AU - Cao, Yin
AU - Chan, Andrew T.
AU - Dimou, Niki
AU - Drew, David A.
AU - French, Amy J.
AU - Georgeson, Peter
AU - Giannakis, Marios
AU - Gruber, Stephen B.
AU - Gunter, Marc J.
AU - Harrison, Tabitha A.
AU - Hoffmeister, Michael
AU - Hsu, Li
AU - Huang, Wen Yi
AU - Hullar, Meredith A.J.
AU - Huyghe, Jeroen R.
AU - Lynch, Brigid M.
AU - Moreno, Victor
AU - Newton, Christina C.
AU - Nowak, Jonathan A.
AU - Obón-Santacana, Mireia
AU - Ogino, Shuji
AU - Qu, Conghui
AU - Schmit, Stephanie L.
AU - Steinfelder, Robert S.
AU - Sun, Wei
AU - Thomas, Claire E.
AU - Toland, Amanda E.
AU - Trinh, Quang M.
AU - Ugai, Tomotaka
AU - Um, Caroline Y.
AU - Van Guelpen, Bethany
AU - Zaidi, Syed H.
AU - Murphy, Neil
AU - Peters, Ulrike
AU - Phipps, Amanda I.
AU - Tsilidis, Konstantinos K.
N1 - Publisher Copyright:
©2025 American Association for Cancer Research.
PY - 2025/4/1
Y1 - 2025/4/1
N2 - Background: Waist circumference (WC) and its allometric counterpart, “a body shape index” (ABSI), are risk factors for colorectal cancer; however, it is uncertain whether associations with these body measurements are limited to specific molecular subtypes of the disease. Methods: Data from 2,772 colorectal cancer cases and 3,521 controls were pooled from four cohort studies within the Genetics and Epidemiology of Colorectal Cancer Consortium. Four molecular markers (BRAF mutation, KRAS mutation, CpG island methylator phenotype, and microsatellite instability) were analyzed individually and in combination (Jass types). Multivariable logistic and multinomial logistic models were used to assess the associations of WC and ABSI with overall colorectal cancer risk and, in case-only analyses, to evaluate heterogeneity by molecular subtype, respectively. Results: Higher WC (ORper 5 cm ¼ 1.06, 95% confidence interval, 1.04–1.09) and ABSI (ORper 1-SD ¼ 1.07, 95% confidence interval, 1.00–1.14) were associated with elevated colorectal cancer risk. There was no evidence of heterogeneity between the molecular subtypes. No difference was observed regarding the influence of WC and ABSI on the four major molecular markers in proximal colon, distal colon, and rectal cancers, as well as in early- and late-onset colorectal cancers. Associations did not differ in the Jass-type analysis. Conclusions: Higher WC and ABSI were associated with elevated colorectal cancer risk; however, they do not differentially influence all four major molecular mutations involved in colorectal carcinogenesis but underscore the importance of maintaining a healthy body weight in colorectal cancer prevention. Impact: The proposed results have potential utility in colorectal cancer prevention.
AB - Background: Waist circumference (WC) and its allometric counterpart, “a body shape index” (ABSI), are risk factors for colorectal cancer; however, it is uncertain whether associations with these body measurements are limited to specific molecular subtypes of the disease. Methods: Data from 2,772 colorectal cancer cases and 3,521 controls were pooled from four cohort studies within the Genetics and Epidemiology of Colorectal Cancer Consortium. Four molecular markers (BRAF mutation, KRAS mutation, CpG island methylator phenotype, and microsatellite instability) were analyzed individually and in combination (Jass types). Multivariable logistic and multinomial logistic models were used to assess the associations of WC and ABSI with overall colorectal cancer risk and, in case-only analyses, to evaluate heterogeneity by molecular subtype, respectively. Results: Higher WC (ORper 5 cm ¼ 1.06, 95% confidence interval, 1.04–1.09) and ABSI (ORper 1-SD ¼ 1.07, 95% confidence interval, 1.00–1.14) were associated with elevated colorectal cancer risk. There was no evidence of heterogeneity between the molecular subtypes. No difference was observed regarding the influence of WC and ABSI on the four major molecular markers in proximal colon, distal colon, and rectal cancers, as well as in early- and late-onset colorectal cancers. Associations did not differ in the Jass-type analysis. Conclusions: Higher WC and ABSI were associated with elevated colorectal cancer risk; however, they do not differentially influence all four major molecular mutations involved in colorectal carcinogenesis but underscore the importance of maintaining a healthy body weight in colorectal cancer prevention. Impact: The proposed results have potential utility in colorectal cancer prevention.
UR - https://www.scopus.com/pages/publications/105002325823
U2 - 10.1158/1055-9965.EPI-24-1534
DO - 10.1158/1055-9965.EPI-24-1534
M3 - Article
C2 - 39898780
AN - SCOPUS:105002325823
SN - 1055-9965
VL - 34
SP - 568
EP - 577
JO - Cancer Epidemiology Biomarkers and Prevention
JF - Cancer Epidemiology Biomarkers and Prevention
IS - 4
ER -