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Risk of cancer in patients with bile acid diarrhoea: a Danish nationwide matched cohort study.
Nyboe Andersen, Nynne; Wildt, Signe; Iversen, Aske Thorn; Poulsen, Gry; Jess, Tine; Munck, Lars Kristian; Borup, Christian.
Affiliation
  • Nyboe Andersen N; Department of Gastroenterology, Zealand University Hospital Koge, Koge, Denmark nynne@nyboeandersen.com.
  • Wildt S; Department of Gastroenterology and Hepatology, Hvidovre Hospital, Hvidovre, Denmark.
  • Iversen AT; Center for Molecular Prediction of Inflammatory Bowel Disease, Department of Clinical Medicine, The Faculty of Medicine, Aalborg University, Copenhagen, Denmark.
  • Poulsen G; Center for Molecular Prediction of Inflammatory Bowel Disease, Department of Clinical Medicine, The Faculty of Medicine, Aalborg University, Copenhagen, Denmark.
  • Jess T; Center for Molecular Prediction of Inflammatory Bowel Disease, Department of Clinical Medicine, The Faculty of Medicine, Aalborg University, Copenhagen, Denmark.
  • Munck LK; Department of Gastroenterology, Zealand University Hospital Koge, Koge, Denmark.
  • Borup C; Department of Gastroenterology, Zealand University Hospital Koge, Koge, Denmark.
BMJ Open Gastroenterol ; 11(1)2024 Apr 30.
Article in En | MEDLINE | ID: mdl-38688717
ABSTRACT

OBJECTIVE:

Bile acid diarrhoea is a common cause of chronic diarrhoea. Increased levels of potentially carcinogenic bile acids in faeces, theoretically, may increase the risk of colorectal cancer in particular, but the long-term disease course is unknown. We aimed to investigate the overall and site-specific cancer risk in bile acid diarrhoea.

DESIGN:

Adult patients with bile acid diarrhoea were identified using nationwide Danish registries from 2003 to 2020 by a diagnostic gold-standard 75-selenium tauroselcholic acid procedure followed within 6 months by sequestrant prescription. The risk of overall and site-specific cancers in cases with bile acid diarrhoea was compared with sex, age and comorbidity-adjusted matched controls. A competing risk model estimated cumulative incidence functions and cause-specific HRs.

RESULTS:

We identified 2260 patients with bile acid diarrhoea with a mean follow-up of 5.5 years (SD 4.2). The overall cancer risk was increased by an HR of 1.32 (95% CI 1.12 to 1.54). The risk of site-specific cancer was increased in 3 of 10 cancer groups haematological, HR 2.41 (1.36 to 4.02); skin, HR 1.33 (1.01 to 1.71); and male genital cancers, HR 1.85 (1.11 to 2.92). No increased risk of colorectal cancer was detected in patients with bile acid diarrhoea, HR 0.73 (0.34 to 1.63).

CONCLUSIONS:

Bile acid diarrhoea was associated with an increased overall risk of cancer, especially haematological cancers, but the risk of colorectal cancer was not increased. The lack of a diagnostic code for bile acid diarrhoea and potential residual confounding are limitations, and the findings should be replicated in other cohorts.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bile Acids and Salts / Diarrhea Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: BMJ Open Gastroenterol Year: 2024 Document type: Article Affiliation country: Denmark Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bile Acids and Salts / Diarrhea Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: BMJ Open Gastroenterol Year: 2024 Document type: Article Affiliation country: Denmark Country of publication: United kingdom