The Safety and Benefit of Statins in Liver Cirrhosis: A Review
Loading...
Date
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
Georg Thieme Verlag
Abstract
Dyslipidemia is a primary, major risk factor for coronary artery disease CAD. The prevalence of dyslipidemia had decreased over the past 30 years, which may in part be explained by the steady increase in the use of lipid-lowering drug therapy, especially statins. Cardiovascular risk has been shown to be greater in liver disease (20% in the liver cirrhosis vs. 12% in the general population), where statins can play an important role as a primary and secondary prevention for CAD. Given patients with chronic liver disease, especially liver cirrhosis are at risk of decreased hepatic clearance, there is concern that this patient population may be at higher risk for complications from statin therapy. Several retrospective studies showed that statin use in chronic liver disease and cirrhosis is safe, and even it was associated with lower mortality and lower rate of hepatic decompensation. This review discusses the safety and the different mechanisms where statins can decrease the rate of complications in liver cirrhosis, including portal hypertension, sepsis and the incidence of hepatocellular carcinoma.
Description
Keywords
Decompensation, Hepatocellular carcinoma, Liver cirrhosis, Safety, Statins, Animals, Coronary artery disease, Humans, Hydroxymethylglutaryl-coa reductase inhibitors, Alanine aminotransferase, Hydroxymethylglutaryl coenzyme a reductase inhibitor, Adverse outcome, Alanine aminotransferase blood level, Antiangiogenic activity, Antimicrobial activity, Antiproliferative activity, Article, Cancer inhibition, Cancer risk, Decompensated liver cirrhosis, Drug exposure, Drug induced disease, Drug mechanism, Drug safety, Drug tolerability, Follow up, Hepatic encephalopathy, Human, Immunomodulation, In vitro study, Inflammation, Liver cell carcinoma, Liver function, Liver function test, Liver injury, Liver perfusion, Liver protection, Liver toxicity, Mortality, Nonhuman, Oxidative stress, Portal hypertension, Priority journal, Risk reduction, Sepsis, Side effect, Survival, Treatment duration, Treatment outcome, Variceal hemorrhage, Animal, Metabolism