Association of inflammatory bowel disease in first‐degree relatives with risk of colorectal cancer: A nationwide case‐control study in Sweden

Author:

Wang Kai1ORCID,Olén Ola234,Emilsson Louise5678,Khalili Hamed91011,Halfvarson Jonas12,Song Mingyang191013ORCID,Ludvigsson Jonas F.71415

Affiliation:

1. Department of Epidemiology Harvard T.H. Chan School of Public Health Boston Massachusetts USA

2. Department of Clinical Science and Education Södersjukhuset Karolinska Institute Stockholm Sweden

3. Clinical Epidemiology Division, Department of Medicine Solna, Karolinska Institute Stockholm Sweden

4. Sachs' Children and Youth Hospital Stockholm South General Hospital Stockholm Sweden

5. Department of General Medicine Institute of Health and Society, University of Oslo Oslo Norway

6. Vårdcentralen Nysäter and Center for Clinical Research County Council of Värmland Värmland Sweden

7. Department of Medical Epidemiology and Biostatistics Karolinska Institute Stockholm Sweden

8. Faculty of Medicine and Health Örebro University Örebro Sweden

9. Clinical and Translational Epidemiology Unit Massachusetts General Hospital Boston Massachusetts USA

10. Division of Gastroenterology Massachusetts General Hospital and Harvard Medical School Boston Massachusetts USA

11. Institute of Environmental Medicine Nutrition Epidemiology, Karolinska Institutet Solna Sweden

12. Department of Gastroenterology Faculty of Medicine and Health, Örebro University Örebro Sweden

13. Department of Nutrition Harvard T. H. Chan School of Public Health Boston Massachusetts USA

14. Department of Pediatrics Örebro University Hospital Örebro Sweden

15. Division of Digestive and Liver Disease, Department of Medicine Columbia University Medical Center New York New York USA

Abstract

AbstractThis study aims to assess the association between inflammatory bowel disease (IBD) history in first‐degree relatives (FDRs) and colorectal cancer (CRC) risk. We conducted a nationwide case‐control study in Sweden among 69 659 CRC cases and 343 032 non‐CRC controls matched on age, sex, birth year and residence county. Through linkage of multi‐generation register and the nationwide ESPRESSO (Epidemiology Strengthened by histoPathology Reports in Sweden) cohort, we ascertained IBD diagnoses among parents, full siblings and offspring of the index individuals. Odds ratios (ORs) of CRC associated with IBD family history were calculated using conditional logistic regression. 2.2% of both CRC cases (1566/69659) and controls (7676/343027) had ≥1 FDR with IBD history. After adjusting for family history of CRC, we observed no increased risk of CRC in FDRs of IBD patients (OR, 0.96; 95%CI, 0.91‐1.02). The null association was consistent according to IBD subtype (Crohn's disease or ulcerative colitis), number of FDRs with IBD (1 or ≥ 2), age at first IBD diagnosis in FDRs (<18, 18‐39, 40‐59 or ≥60 years), maximum location/extent of IBD or FDR relation (parent, sibling or offspring). The null association remained for early‐onset CRC (diagnosed at age <50 years). In conclusion, IBD history in FDRs was not associated with an increased risk of CRC. Our findings suggest that extra screening for CRC may not be needed in the offspring, siblings or parents of IBD patients, and strengthen the theory that it is the actual inflammation or atypia of the colon in IBD patients that confers the increased CRC risk.

Funder

American Cancer Society

National Institutes of Health

Swedish Cancer Foundation

Vetenskapsrådet

Publisher

Wiley

Subject

Cancer Research,Oncology

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