TY - JOUR
T1 - Antibiotic Therapy and Risk of Early-Onset Colorectal Cancer
T2 - A National Case-Control Study
AU - Nguyen, Long H.
AU - Cao, Yin
AU - Batyrbekova, Nurgul
AU - Roelstraete, Bjorn
AU - Ma, Wenjie
AU - Khalili, Hamed
AU - Song, Mingyang
AU - Chan, Andrew T.
AU - Ludvigsson, Jonas F.
N1 - Funding Information:
Financial support : J.F.L. coordinates a study on behalf of the Swedish IBD Quality Register (SWIBREG). This study has received funding from Janssen Corporation. This work was supported by the National Institutes of Health and the National Institute of Diabetes and Digestive and Kidney Disease (K23DK125838 to L.H.N.); the American Gastroenterological Association (Research Scholars Award to L.H.N.); the Crohn's and Colitis Foundation (Research Fellowship Award and Career Development Award to L.H.N. and Senior Investigator Award to A.T.C. and H.K.); the National Cancer Institute (R01CA202704 and R35 CA253185 to A.T.C.; R00CA215314 to MS); the American Cancer Society (MRSG-17-220-01—NEC to M.S.); and the Massachusetts General Hospital (Stuart and Suzanne Steel Research Scholars Award to A.T.C.).
Publisher Copyright:
© 2022 Lippincott Williams and Wilkins. All rights reserved.
PY - 2022/1/13
Y1 - 2022/1/13
N2 - INTRODUCTION:Antibiotic use has emerged as a risk factor for colorectal neoplasia and is hypothesized as a contributor to the rising incidence of colorectal cancer under age 50 years or early-onset colorectal cancer (EOCRC). However, the impact of antibiotic use and risk of EOCRC is unknown.METHODS:We conducted a population-based case-control study of CRC among individuals aged ≥18 years in the Epidemiology Strengthened by histoPathology Reports in Sweden (ESPRESSO) cohort (2006-2016). The primary outcome was EOCRC. A secondary outcome was CRC at any age. Incident CRC was pathologically confirmed, and for each, up to 5 population-based controls were matched on age, sex, county of residence, and calendar year. We assessed prescriptions until 6 months before CRC diagnosis. Conditional logistic regression was used to estimate adjusted odds ratios (aORs) and 95% confidence intervals (CIs).RESULTS:We identified 54,804 cases of CRC (2,557 EOCRCs) and 261,089 controls. Compared with none, previous antibiotic use was not associated with EOCRC risk after adjustment for potential confounders (aOR 1.06, 95% CI: 0.96, 1.17) with similarly null findings when stratified by anatomic tumor site. In contrast, previous antibiotic use was weakly associated with elevated risk for CRC at any age (aOR 1.05, 95% CI: 1.02, 1.07). A potential but modest link between broad-spectrum antibiotic use and EOCRC was observed (aOR 1.13, 95% CI: 1.02, 1.26).DISCUSSION:We found no conclusive evidence that antibiotics are associated with EOCRC risk. Although antibiotic use was weakly associated with risk of CRC at any age, the magnitude of association was modest, and the study period was relatively short.
AB - INTRODUCTION:Antibiotic use has emerged as a risk factor for colorectal neoplasia and is hypothesized as a contributor to the rising incidence of colorectal cancer under age 50 years or early-onset colorectal cancer (EOCRC). However, the impact of antibiotic use and risk of EOCRC is unknown.METHODS:We conducted a population-based case-control study of CRC among individuals aged ≥18 years in the Epidemiology Strengthened by histoPathology Reports in Sweden (ESPRESSO) cohort (2006-2016). The primary outcome was EOCRC. A secondary outcome was CRC at any age. Incident CRC was pathologically confirmed, and for each, up to 5 population-based controls were matched on age, sex, county of residence, and calendar year. We assessed prescriptions until 6 months before CRC diagnosis. Conditional logistic regression was used to estimate adjusted odds ratios (aORs) and 95% confidence intervals (CIs).RESULTS:We identified 54,804 cases of CRC (2,557 EOCRCs) and 261,089 controls. Compared with none, previous antibiotic use was not associated with EOCRC risk after adjustment for potential confounders (aOR 1.06, 95% CI: 0.96, 1.17) with similarly null findings when stratified by anatomic tumor site. In contrast, previous antibiotic use was weakly associated with elevated risk for CRC at any age (aOR 1.05, 95% CI: 1.02, 1.07). A potential but modest link between broad-spectrum antibiotic use and EOCRC was observed (aOR 1.13, 95% CI: 1.02, 1.26).DISCUSSION:We found no conclusive evidence that antibiotics are associated with EOCRC risk. Although antibiotic use was weakly associated with risk of CRC at any age, the magnitude of association was modest, and the study period was relatively short.
UR - http://www.scopus.com/inward/record.url?scp=85124437722&partnerID=8YFLogxK
U2 - 10.14309/ctg.0000000000000437
DO - 10.14309/ctg.0000000000000437
M3 - Article
C2 - 35029165
AN - SCOPUS:85124437722
SN - 2155-384X
VL - 13
SP - E00437
JO - Clinical and Translational Gastroenterology
JF - Clinical and Translational Gastroenterology
IS - 1
ER -