Cited by 173Drug-Induced Hepatotoxicity and ProtectionLiver Disease Diagnosis and TreatmentLipoproteins and Cardiovascular Health

Lipid-lowering agents that cause drug-induced hepatotoxicity.

Open access
Bhardwaj, Sidharth S., Chalasani, Naga·2007·Clinics in Liver Disease

Abstract

The effort to reduce cardiovascular risk factors, including hyperlipidemia, has led to the increased use of lipid-lowering agents. Hyperlipidemic patients often have underlying fatty liver disease, however, and thus may have elevated and fluctuating liver biochemistries. Therefore, caution should be applied before attributing elevated liver tests to lipid-lowering agents. Data indicate that patients who have chronic liver disease and compensated cirrhosis should not be precluded from receiving statins to treat hyperlipidemia. Several recent studies and expert opinion currently fully endorse statin use in patients who have nonalcoholic fatty liver disease and other chronic liver disease if clinically indicated.

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Crossref · 10.1016/j.cld.2007.06.010

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  • The most serious complication of niacin therapy is hepatotoxicity, which is dose dependent, and therapy should be accompanied by monitoring of liver function tests.

    “The most serious complication of niacin therapy is hepatotoxicity (which is dose dependent), and therapy should be accompanied by monitoring of liver function tests (178).”

    From Evaluation and Treatment of Hypertriglyceridemia: An Endocrine Society Clinical Practice Guideline (2012) · cites this paper as [178]

    The Niacin section (page unavailable) describes dose-related hepatotoxicity, especially with sustained-release niacin, and the Conclusion calls sustained-release niacin a cause of clinically significant liver injury. The passages do not recommend monitoring liver function tests during niacin therapy, so that part of the claim is unsupported. (LLM, conf=0.86)

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Research works printed but not linked: 1

  1. Jacobson TA. Statin safety: lessons from new drug applications for marketed statins. American Journal of Cardiology 2006;97(suppl):44C-51C. [PubMed: 16377282]

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Authors
Bhardwaj, S. S., & Chalasani, N.
Affiliations
Indiana University Indianapolis (US)
Corresponding author
Chalasani, Naga
Venue
Clinics in Liver Disease
Publisher
Elsevier BV
Published
2007-08
Volume
11
Issue
3
Pages
597-613
ISSN
1089-3261 (ISSN-L)
OpenAlex
W2089712819
Cited by
173
References
89
Citations by year
2026: 4 · 2025: 9 · 2024: 9 · 2023: 5 · 2022: 13 · 2021: 9 · 2020: 7 · 2019: 12 · 2018: 10 · 2017: 14 · 2016: 7 · 2015: 10 · 2014: 11 · 2013: 9 · 2012: 10
FWCI
0.97
Type
journal article
Language
en
Open access
Locations
  • Clinics in Liver Disease (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • IUScholarWorks (Indiana University) (submittedVersion)
Funders
  • U.S. Public Health Service (K24 069290)
  • National Institute of Diabetes and Digestive and Kidney Diseases (K24DK069290)
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Drug-Induced Hepatotoxicity and Protection
  • Health Sciences › Medicine › Epidemiology › Liver Disease Diagnosis and Treatment
  • Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
Keywords
lipid-lowering drugs, drug-induced liver injury, statins, hyperlipidemia, non-alcoholic fatty liver disease, chronic liver disease, compensated cirrhosis, liver function tests, cardiovascular risk reduction
MeSH terms
Ezetimibe, Hypolipidemic Agents, Azetidines, Humans, Niacin, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Cholesterol Ester Transfer Proteins, Chemical and Drug Induced Liver Injury

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