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Association of genetic liability to allergic diseases with overall and early-onset colorectal cancer risk: a mendelian randomization study
Public Health Department, College of Public Health, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
Department of Oncology, Early Cancer Institute, University of Cambridge, Cambridge, United Kingdom.
Department of Epidemiology and Biostatistics, Institute of Systems Epidemiology, West China-PUMC C. C. Chen Institute of Health, West China School of Public Health, West China Fourth Hospital, Sichuan University, Chengdu, China; Department of Nutrition and Food Hygiene, West China School of Public Health, West China Fourth Hospital, Sichuan University, Chengdu, China; Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, Solna, Sweden.
Department of Emergency Medicine, Massachusetts General Hospital, Harvard Medical School, MA, Boston, United States.
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2025 (English)In: Cancer Epidemiology, Biomarkers and Prevention, ISSN 1055-9965, E-ISSN 1538-7755, Vol. 34, no 5, p. 722-736Article in journal (Refereed) Published
Abstract [en]

Background: The tumor immunosurveillance theory supports that allergic conditions could decrease cancer risk. However, observational evidence yielded inconsistent results for the association between allergic diseases and colorectal cancer risk. We used Mendelian randomization (MR) to examine potential causal associations of allergies with the risk of overall and early-onset colorectal cancer.

Methods: Genome-wide association study summary statistical data were used to identify genetic variants associated with allergic diseases (Nvariants = 65) and individual allergic conditions (asthma, hay fever/allergic rhinitis, and eczema). Using twosample MR, we examined these variants in relation to incident overall (Ncases = 52,775 cases) and early-onset colorectal cancer (Ncases = 6,176). The mediating role of white blood cells was examined using multivariable MR.

Results: In inverse-variance-weighted models, genetic liability to allergic diseases was inversely associated with overall {OR per log (odds) = 0.90 [95% confidence interval (CI), 0.85-0.96]; P < 0.01} and early-onset colorectal cancer [OR = 0.83 (95% CI, 0.73-0.95); P = 0.01]. Similar inverse associations were found for hay fever/allergic rhinitis or eczema, whereas no evidence of association was found between liability to asthma-related phenotypes and colorectal cancer risk. Multivariable MR adjustment for eosinophils weakened the inverse associations for liability to allergic diseases for overall [OR = 0.96 (95% CI, 0.89-1.03); P = 0.26] and early-onset colorectal cancer [OR = 0.86 (95% CI, 0.73-1.01); P = 0.06].

Conclusions: Our study supports a potential causal association between liability to allergic diseases, specifically hay fever/allergic rhinitis or eczema, and colorectal cancer, possibly at least in part mediated via eosinophil counts.

Impact: Our results provide evidence that allergic responses may also have a role in immunosurveillance against colorectal cancer.

Place, publisher, year, edition, pages
American Association For Cancer Research (AACR), 2025. Vol. 34, no 5, p. 722-736
National Category
Medical Genetics and Genomics
Identifiers
URN: urn:nbn:se:umu:diva-238730DOI: 10.1158/1055-9965.EPI-24-0970PubMedID: 39982694Scopus ID: 2-s2.0-105004370569OAI: oai:DiVA.org:umu-238730DiVA, id: diva2:1958019
Funder
Region VästerbottenGerman Research Foundation (DFG)Region SkåneSwedish Cancer SocietySwedish Research CouncilUmeå UniversityAvailable from: 2025-05-13 Created: 2025-05-13 Last updated: 2025-05-13Bibliographically approved

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van Guelpen, Bethany

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