期刊
CLINICAL PHARMACOKINETICS
卷 62, 期 8, 页码 1141-1155出版社
ADIS INT LTD
DOI: 10.1007/s40262-023-01261-3
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In this study, the impact of liver cirrhosis on the activity of UDP-glucuronosyltransferases (UGTs) was investigated. It was found that liver cirrhosis may affect the activity of UGTs according to liver function, with significant changes in glucuronidation capacity observed in some substrates in patients with liver cirrhosis. However, clinically significant glucuronide accumulation did not occur in the population studied.
Background and ObjectiveThe impact of liver cirrhosis on the activity of UDP-glucuronosyltransferases (UGTs) is currently not well characterized. We investigated the glucuronidation capacity and glucuronide accumulation in patients with liver cirrhosis.MethodsWe administered the Basel phenotyping cocktail (caffeine, efavirenz, flurbiprofen, omeprazole, metoprolol, midazolam) to patients with liver cirrhosis (n = 16 Child A, n = 15 Child B, n = 5 Child C) and n = 12 control subjects and obtained pharmacokinetic profiles of substrates and primary metabolites and their glucuronides.ResultsCaffeine and its metabolite paraxanthine were only slightly glucuronidated. The metabolic ratio (AUC(glucuronide)/AUC(parent), MR) was not affected for caffeine but decreased by 60% for paraxanthine glucuronide formation in Child C patients. Efavirenz was not glucuronidated whereas 8-hydroxyefavirenz was efficiently glucuronidated. The MR of 8-hydroxyefavirenz-glucuronide formation increased three-fold in Child C patients and was negatively correlated with the glomerular filtration rate. Flurbiprofen and omeprazole were not glucuronidated. 4-Hydroxyflurbiprofen and 5-hydroxyomeprazole were both glucuronidated but the corresponding MRs for glucuronide formation were not affected by liver cirrhosis. Metoprolol, but not alpha-hydroxymetoprolol, was glucuronidated, and the MR for metoprolol-glucuronide formation dropped by 60% in Child C patients. Both midazolam and its metabolite 1 '-hydroxymidazolam underwent glucuronidation, and the corresponding MRs for glucuronide formation dropped by approximately 80% in Child C patients. No relevant glucuronide accumulation occurred in patients with liver cirrhosis.ConclusionsDetailed analysis revealed that liver cirrhosis may affect the activity of UGTs of the UGT1A and UGT2B subfamilies according to liver function. Clinically significant glucuronide accumulation did not occur in the population investigated.
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