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ABSTRACT: Background
Terlipressin is the only FDA-approved vasoconstrictor for hepatorenal syndrome (HRS). The CONFIRM study is the largest trial of terlipressin versus placebo. Novel predictors of HRS response are required to enrich patient selection and optimize outcomes.Methods
Samples at treatment initiation were tested using (a) liquid chromatography-mass spectrometry of 1594 plasma/1420 urine metabolites (Metabolon Inc.), (b) aptamer-based array of 7289 plasma proteins (SomaScan), and (c) 14 plasma/urine pre-specified assays. The CONFIRM trial's original definition of HRS response [2 serum creatinine (SCr) <1.5 mg/dL separated by >2 h] was used as the primary outcome.Results
In all, 115 patients [79 terlipressin-treated (TT) and 36 placebo-treated (PT)] provided samples
SUBMITTER: Allegretti AS
PROVIDER: S-EPMC12262949 | biostudies-literature | 2025 Aug
REPOSITORIES: biostudies-literature