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Statins Are Associated With a Decreased Risk of Severe Liver Disease in Individuals With Noncirrhotic Chronic Liver
Rajani Sharma1, Tracey G Simon2, Hannes Hagström3
1Center for Liver Disease and Transplantation, Division of Digestive and Liver Diseases, Columbia University Irving Medical Center, New York, New York; Division of Digestive and Liver Diseases, Department of Medicine, Columbia University College of Physicians and Surgeons, New York, New York.
Insights
Statins may slow the progression of chronic liver disease (CLD) to severe outcomes. This study found statin use was linked to a reduced risk of developing severe liver disease in noncirrhotic patients.
Area of Science:
- Hepatology
- Pharmacology
- Epidemiology
Background:
- Chronic liver diseases (CLDs) can progress to severe liver conditions.
- The impact of statins on noncirrhotic CLD progression is not well understood.
Purpose of the Study:
- To investigate the association between statin use and the risk of severe liver disease in patients with noncirrhotic CLD.
Main Methods:
- A nationwide Swedish cohort study identified 3862 noncirrhotic CLD patients with statin exposure.
- Matched statin users and non-users using propensity score matching.
- Cox regression analysis to assess the risk of incident severe liver disease.
Main Results:
- Statin use was associated with a 40% reduced risk of severe liver disease (HR, 0.60).
- Protective effects were observed in alcohol-related liver disease and nonalcoholic fatty liver disease.
- Statin use lowered rates of progression to cirrhosis, hepatocellular carcinoma, and liver-related mortality.
Conclusions:
- Incident statin use in noncirrhotic CLD patients is associated with lower rates of severe liver disease.
- Statins may play a disease-modifying role in noncirrhotic chronic liver disease.
Background & Aims:
Little is known about the potential impact of statins on the progression of noncirrhotic chronic liver diseases (CLDs) to severe liver disease.
Methods:
Using liver histopathology data in a nationwide Swedish cohort, we identified 3862 noncirrhotic individuals with CLD and statin exposure, defined as a statin prescription filled for 30 or more cumulative defined daily doses. Statin users were matched to 3862 (statin) nonusers with CLD through direct 1:1 matching followed by propensity score matching. Cox regression was used to estimate hazard ratios (HRs) for the primary outcome of incident severe liver disease (a composite of cirrhosis, hepatocellular carcinoma, and liver transplantation/liver-related mortality).
Results:
A total of 45.3% of CLD patients had nonalcoholic fatty liver disease, 21.9% had alcohol-related liver disease, 17.7% had viral hepatitis, and 15.1% had autoimmune hepatitis. During follow-up evaluation, 234 (6.1%) statin users vs 276 (7.1%) nonusers developed severe liver disease. Statin use was associated with a decreased risk of developing severe liver disease (HR, 0.60; 95% CI, 0.48-0.74). Statistically significantly lower rates of severe liver disease were seen in alcohol-related liver disease (HR, 0.30; 95% CI, 0.19-0.49) and in nonalcoholic fatty liver disease (HR, 0.68; 95% CI, 0.45-1.00), but not in viral hepatitis (HR, 0.76; 95% CI, 0.51-1.14) or autoimmune hepatitis (HR, 0.88; 95% CI, 0.48-1.58). Statin use had a protective association in both prefibrosis and fibrosis stages at diagnosis. Statin use was associated with lower rates of progression to cirrhosis (HR, 0.62; 95% CI, 0.49-0.78), hepatocellular carcinoma (HR, 0.44; 95% CI, 0.27-0.71), and liver-related mortality (HR, 0.55; 95% CI, 0.36-0.82).
Conclusions:
Among individuals with noncirrhotic CLD, incident statin use was linked to lower rates of severe liver disease, suggesting a potential disease-modifying role.
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