The primary cause of markedly elevated aminotransferases in hospitalized patients with cirrhosis in ischemic hepatitis

Eur J Gastroenterol Hepatol. 2024 Nov 1;36(11):1346-1351. doi: 10.1097/MEG.0000000000002855. Epub 2024 Sep 25.

Abstract

Background: Marked elevation in aminotransferases (≥1000 IU/l) is typically associated with acute liver injury. Here, we hypothesized that the cause of elevation in aminotransferases ≥1000 in patients with cirrhosis is likely due to a limited number of disorders and may be associated with poor outcomes.

Aim: We aimed to investigate the most common etiologies of acute elevations in aminotransferases in patients with cirrhosis, and to examine their associated outcomes.

Methods: From May 2012 to December 2022, all hospitalized patients with cirrhosis and an aspartate aminotransferase or alanine aminotransferase ≥ 1000 IU/l were identified through Medical University of South Carolina's Clinical Data Warehouse. Complete clinical data were abstracted for each patient, and in-hospital mortality was examined.

Results: The cohort was made up of 152 patients, who were 57 ± 12 years old, with 51 (34%) women. Underlying liver disease included mainly hepatitis C cirrhosis, alcohol-related cirrhosis, metabolic dysfunction-associated steatohepatitis cirrhosis, autoimmune cirrhosis, primary sclerosing cholangitis cirrhosis, and cryptogenic cirrhosis. The most common cause of marked elevation in aminotransferases in cirrhotic patients was ischemic hepatitis (71%), followed by chemoembolization (7%), autoimmune hepatitis (6%), drug-induced liver injury (3%), post-transjugular intrahepatic portosystemic shunt placement (3%), rhabdomyolysis (3%), and hepatitis C (2%). During hospitalization and over a 1-month follow-up period, the mortality rate in patients with ischemic hepatitis was 73% (79/108), while that for other causes of liver injury was 20% (9/44).

Conclusion: Ischemic hepatitis is the leading cause of marked elevation of aminotransferases in patients with cirrhosis, with distinctive clinical characteristics than other etiologies, and significantly poorer outcomes.

MeSH terms

  • Adult
  • Aged
  • Alanine Transaminase* / blood
  • Aspartate Aminotransferases* / blood
  • Biomarkers / blood
  • Female
  • Hepatitis / complications
  • Hospital Mortality*
  • Hospitalization*
  • Humans
  • Ischemia / etiology
  • Liver Cirrhosis* / complications
  • Male
  • Middle Aged
  • Retrospective Studies

Substances

  • Alanine Transaminase
  • Aspartate Aminotransferases
  • Biomarkers