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Statin use and risk of colorectal cancer in patients with inflammatory bowel disease.
Sun, Jiangwei; Halfvarson, Jonas; Bergman, David; Ebrahimi, Fahim; Roelstraete, Bjorn; Lochhead, Paul; Song, Mingyang; Olén, Ola; Ludvigsson, Jonas F.
Affiliation
  • Sun J; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Halfvarson J; Department of Gastroenterology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
  • Bergman D; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Ebrahimi F; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Roelstraete B; Department of Gastroenterology and Hepatology, Clarunis - University Center for Gastrointestinal and Liver Diseases, Basel, Switzerland.
  • Lochhead P; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
  • Song M; Medicines Research Centre, GSK, Stevenage, UK.
  • Olén O; Departments of Epidemiology and Nutrition, Harvard T.H. Chan School of Public Health, Harvard University, Boston, MA, USA.
  • Ludvigsson JF; Clinical and Translational Epidemiology Unit and Division of Gastroenterology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
EClinicalMedicine ; 63: 102182, 2023 Sep.
Article de En | MEDLINE | ID: mdl-37662517
ABSTRACT

Background:

Statin use has been linked to a reduced risk of advanced colorectal adenomas, but its association with colorectal cancer (CRC) in patients with inflammatory bowel disease (IBD) - a high risk population for CRC - remains inconclusive.

Methods:

From a nationwide IBD cohort in Sweden, we identified 5273 statin users and 5273 non-statin users (11 propensity score matching) from July 2006 to December 2018. Statin use was defined as the first filled prescription for ≥30 cumulative defined daily doses and followed until December 2019. Primary outcome was incident CRC. Secondary outcomes were CRC-related mortality and all-cause mortality. Cox regression estimated adjusted hazard ratios (aHRs) and 95% confidence intervals (CIs).

Findings:

During a median follow-up of 5.6 years, 70 statin users (incidence rate (IR) 21.2 per 10,000 person-years) versus 90 non-statin users (IR 29.2) were diagnosed with incident CRC (rate difference (RD), -8.0 (95% CIs -15.8 to -0.2 per 10,000 person-years); aHR = 0.76 (95% CIs 0.61 to 0.96)). The benefit for incident CRC was duration-dependent in a nested case-control

design:

as compared to short-term use (30 days to <1 year), the adjusted odd ratios were 0.59 (0.25 to 1.43) for 1 to <2 years of use, 0.46 (0.21 to 0.98) for 2 to <5 years of use, and 0.38 (0.16 to 0.86) for ≥5 years of use (Pfor tread = 0.016). Compared with non-statin users, statin users also had a decreased risk for CRC-related mortality (IR 6.0 vs. 11.9; RD, -5.9 (-10.5 to -1.2); aHR, 0.56 (0.37 to 0.83)) and all-cause mortality (IR 156.4 vs. 231.4; RD, -75.0 (-96.6 to -53.4); aHR, 0.63 (0.57 to 0.69)).

Interpretation:

Statin use was associated with a lower risk of incident CRC, CRC-related mortality, and all-cause mortality. The benefit for incident CRC was duration-dependent, with a significantly lower risk after ≥2 years of statin use.

Funding:

This research was supported by Forte (i.e., the Swedish Research Council for Health, Working Life and Welfare).
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Etiology_studies / Prognostic_studies / Risk_factors_studies Langue: En Journal: EClinicalMedicine Année: 2023 Type de document: Article Pays d'affiliation: Suède

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Etiology_studies / Prognostic_studies / Risk_factors_studies Langue: En Journal: EClinicalMedicine Année: 2023 Type de document: Article Pays d'affiliation: Suède
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