Liver injury associated with endothelin receptor antagonists: a pharmacovigilance study based on FDA adverse event reporting system data

Author:

Gu Jinjian1ORCID,Guo Yuting2,Wu Bin2,He Jinhan1

Affiliation:

1. Sichuan University West China School of Pharmacy

2. West China Hospital of Sichuan University

Abstract

Abstract

Background Endothelin receptor antagonists are commonly used in clinical practice, with concerns about their hepatotoxicity. Aim This study aimed to conduct a comprehensive pharmacovigilance study based on FDA adverse event reporting system data to evaluate the possible association between endothelin receptor antagonists and drug-induced liver injury. Method Adverse event reports from FDA adverse event reporting system between January 2004 and December 2022 were analyzed. Disproportionality algorithms, including reporting odds ratio and information component, were used to evaluate the association between endothelin receptor antagonists and liver injury. Sex- and age-stratified analyses of drug-induced liver injury events were also conducted in relation to endothelin receptor antagonists. Results Significant associations between bosentan, macitentan, and liver injury were identified. Bosentan showed a strong link with liver injury, with reporting odds ratios for cholestatic injury at 7.59 (95% confidence interval: 6.90–8.35), hepatocellular injury at 5.63 (5.29-6.00), and serious drug-related hepatic disorders events at 1.33 (1.24–1.43). It also indicated drug-induced liver injury signals across all age groups. Macitentan was associated with liver injury, with reporting odds ratios for hepatic failure at 1.64 (1.39–1.94), cholestatic injury at 1.62 (1.43–1.83), and serious drug-related hepatic disorders events at 1.40 (1.29–1.51). No drug-induced liver injury signal was detected for ambrisentan, and no significant sex differences were observed in drug-induced liver injury events. Conclusion Both bosentan and macitentan are associated with liver injury. Routine monitoring of serum aminotransferase levels is recommended, especially in patients at higher risk of liver injury. Further research into drug-drug interactions involving Endothelin receptor antagonists is warranted.

Publisher

Research Square Platform LLC

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