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Association of Aspirin with Hepatocellular Carcinoma and Liver-Related Mortality
Division of Gastroenterology and Hepatology, Massachusetts General Hospital, Harvard Medical School, United States; Clinical and Translational Epidemiology Unit, Massachusetts General Hospital, Harvard Medical School, United States; Department of Medicine, Massachusetts General Hospital, Harvard Medical School, United States.
Department of Infectious Diseases, School of Medical Sciences, Faculty of Medicine and Health;, Örebro University Hospital, Örebro, Sweden.ORCID iD: 0000-0001-7248-0910
Department of Infectious Diseases, Karolinska University Hospital, Sweden; Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.
Division of Gastroenterology and Hepatology, Massachusetts General Hospital, Harvard Medical School, United States; Department of Medicine, Massachusetts General Hospital, Harvard Medical School, United States; Broad Institute, Harvard T.H. Chan School of Public Health, Boston, United States.
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2020 (English)In: New England Journal of Medicine, ISSN 0028-4793, E-ISSN 1533-4406, Vol. 382, no 11, p. 1018-1028Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: More information is needed about the long-term effects of low-dose aspirin (≤160 mg) on incident hepatocellular carcinoma, liver-related mortality, and gastrointestinal bleeding in persons with chronic hepatitis B or hepatitis C virus infection.

METHODS: Using nationwide Swedish registries, we identified all adults who received a diagnosis of chronic hepatitis B or hepatitis C from 2005 through 2015 and who did not have a history of aspirin use (50,275 patients). Patients who were starting to take low-dose aspirin (14,205 patients) were identified by their first filled prescriptions for 90 or more consecutive doses of aspirin. We constructed a propensity score and applied inverse probability of treatment weighting to balance baseline characteristics between groups. Using Cox proportional-hazards regression modeling, we estimated the risk of hepatocellular carcinoma and liver-related mortality, accounting for competing events.

RESULTS: With a median of 7.9 years of follow-up, the estimated cumulative incidence of hepatocellular carcinoma was 4.0% among aspirin users and 8.3% among nonusers of aspirin (difference, -4.3 percentage points; 95% confidence interval [CI], -5.0 to -3.6; adjusted hazard ratio, 0.69; 95% CI, 0.62 to 0.76). This inverse association appeared to be duration-dependent; as compared with short-term use (3 months to <1 year), the adjusted hazard ratios were 0.90 (95% CI, 0.76 to 1.06) for 1 to less than 3 years of use, 0.66 (95% CI, 0.56 to 0.78) for 3 to less than 5 years of use, and 0.57 (95% CI, 0.42 to 0.70) for 5 or more years of use. Ten-year liver-related mortality was 11.0% among aspirin users and 17.9% among nonusers (difference, -6.9 percentage points [95% CI, -8.1 to -5.7]; adjusted hazard ratio, 0.73 [95% CI, 0.67 to 0.81]). However, the 10-year risk of gastrointestinal bleeding did not differ significantly between users and nonusers of aspirin (7.8% and 6.9%, respectively; difference, 0.9 percentage points; 95% CI, -0.6 to 2.4).

CONCLUSIONS: In a nationwide study of patients with chronic viral hepatitis in Sweden, use of low-dose aspirin was associated with a significantly lower risk of hepatocellular carcinoma and lower liver-related mortality than no use of aspirin, without a significantly higher risk of gastrointestinal bleeding. (Funded by the National Institutes of Health and others.).

Place, publisher, year, edition, pages
Massachussetts Medical Society , 2020. Vol. 382, no 11, p. 1018-1028
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Medical and Health Sciences Infectious Medicine
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URN: urn:nbn:se:oru:diva-81583DOI: 10.1056/NEJMoa1912035ISI: 000519914300008PubMedID: 32160663Scopus ID: 2-s2.0-85081675148OAI: oai:DiVA.org:oru-81583DiVA, id: diva2:1428628
Available from: 2020-05-06 Created: 2020-05-06 Last updated: 2021-02-04Bibliographically approved

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Duberg, Ann-SofiLudvigsson, Jonas F.

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