Liraglutide-induced autoimmune hepatitis.
JAMA Intern Med · 2014
Last updated 2026-05-28A young woman with type 2 diabetes developed severe liver inflammation after taking the GLP-1 drug liraglutide for 4 months. Her liver function tests showed very high levels of enzymes (AST 991 U/L, ALT 1123 U/L) and bilirubin (9.5 mg/dL), and a liver biopsy revealed damage consistent with autoimmune hepatitis. Stopping the drug worsened her condition, leading to massive liver cell death, but treatment with prednisone improved her symptoms. This is the first reported case of liraglutide causing autoimmune hepatitis, suggesting possible liver risks with this class of drugs.
AI summary of the abstract below.
| Journal | JAMA Intern Med, 2014 |
|---|---|
| Citations | 22 |
| Relative citation ratio | 0.71 |
| NIH percentile | 39 |
| Molecules | liraglutide |
Abstract
IMPORTANCE: Use of incretin-based hypoglycemic agents is increasing, but safety data remain limited. We treated a woman with marker-negative autoimmune hepatitis associated with the glucagon-like peptide 1 agonist liraglutide.
OBSERVATIONS: A young woman with type 2 diabetes mellitus and vitiligo presented with a 10-day history of acute hepatitis. Other than starting liraglutide therapy 4 months prior, she reported no changes in medication therapy and no use of supplements. At admission, aspartate aminotransferase level was 991 U/L; alanine aminotransferase level, 1123 U/L; total bilirubin level, 9.5 mg/dL; and international normalized ratio, 1.3. Results of a liver biopsy demonstrated interface hepatitis with prominent eosinophils and rare plasma cells. The patient's liraglutide therapy was withheld at discharge but her symptoms worsened. A second biopsy specimen revealed massive hepatic necrosis. She started oral prednisone therapy for presumed liraglutide-induced marker-negative autoimmune hepatitis.
CONCLUSIONS AND RELEVANCE: This case represents, to our knowledge, the first report of liraglutide-induced autoimmune hepatitis. Hepatotoxicity may be an incretin analogue class effect with a long latency period. This case raises prescriber awareness about the potential adverse effects of glucagon-like peptide 1 agonists. Postmarketing studies are needed to define the hepatotoxic potential of these agents.
Verbatim abstract via PubMed 24733687 ↗
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