Association of AST/ALT ratio with 90-day outcomes in patients with acute exacerbation of chronic liver disease: a prospective multicenter cohort study in China

Front Med (Lausanne). 2024 Mar 21:11:1307901. doi: 10.3389/fmed.2024.1307901. eCollection 2024.

Abstract

Background and aim: A high aspartate aminotransferase/alanine aminotransferase (AST/ALT) ratio is associated with liver injury in liver disease; however, no data exist regarding its relationship with 90-day prognosis in patients with acute exacerbation of chronic liver disease.

Methods: In this study, 3,758 participants (955 with advanced fibrosis and 2,803 with cirrhosis) from the CATCH-LIFE cohort in China were included. The relationships between different AST/ALT ratios and the risk of adverse 90-day outcomes (death or liver transplantation) were determined in patients with cirrhosis or hepatitis B virus (HBV)-associated advanced fibrosis, respectively.

Results: In the patients with HBV-associated advanced fibrosis, the risk of 90-day adverse outcomes increased with AST/ALT ratio; after adjusting for all confounding factors, the risk of adverse 90-day outcomes was the highest when AST/ALT ratio was more than 1.08 (OR = 6.91 [95% CI = 1.789-26.721], p = 0.005), and the AST/ALT ratio of >1.9 accelerated the development of adverse outcomes. In patients with cirrhosis, an AST/ALT ratio > 1.38 increased the risk of adverse 90-day outcomes in all univariables (OR = 1.551 [95% CI = 1.216-1.983], p < 0.001) and multivariable-adjusted analyses (OR = 1.847 [95% CI = 1.361-2.514], p < 0.001), and an elevated AST/ALT ratio (<2.65) accelerated the incidence of 90-day adverse outcomes. An AST/ALT ratio of >1.38 corresponded with a more than 20% incidence of adverse outcomes in patients with cirrhosis.

Conclusion: The AST/ALT ratio is an independent risk factor for adverse 90-day outcomes in patients with cirrhosis and HBV-associated advanced fibrosis. The cutoff values of the AST/ALT ratio could help clinicians monitor the condition of patients when making clinical decisions.

Keywords: advanced fibrosis; aspartate aminotransferase/alanine aminotransferase ratio; cirrhosis; prognosis; risk factor; short-term outcome.

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was supported by the Shanghai Hospital Development Commission (16CR1024B and SHDC2020CR1037B); National Science and Technology Major Project (2018ZX10302206 and SQ2017YFSF090159); Shanghai Municipal Education Commission—Gaofeng Clinical Medicine Grant Support; Chongqing Natural Science Foundation (CSTC2019jcyj-zdxmX0004); National Natural Science Foundation of China (81930061, 81900579, 81473641, 81271884, 81461130019, 81700561, 81660333, and 81870425); National Natural Science Foundation of China National Science and Technology Major Project (2018ZX10723203); Beijing Natural Science Foundation (7232328); Department of Science and Technology of Guangdong Province (2015B020226004); Foundation for Innovative Research Groups of the Natural Science Foundation of Hubei Province of China (2018CFA031); National Science and Technology Major Project (2017ZX10202202); National Key Research Plan “Precision Medicine Research” Key Project (2017YFC0908103); Shandong Province Natural Science Foundation (ZR2019PH052); 12–5 State S&T Projects of China (2018ZX10302-206); Capital health development research project (2024–1-2173).