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Inter- and Intra-individual Variation, and Limited Prognostic Utility, of Serum Alkaline Phosphatase in a Trial of Patients With Primary Sclerosing Cholangitis

Trivedi, Palak J.; Muir, Andrew J.; Levy, Cynthia; Bowlus, Christopher L.; Manns, Michael P.; Lu, Xiaomin; Crans, Gerald; Chung, Chuhan; Subramanian, G. Mani; Myers, Robert P.; Goodman, Zachary; Chalasani, Naga; Vierling, John M.; Guha, Indra Neil; Hirschfield, Gideon M.

Authors

Palak J. Trivedi

Andrew J. Muir

Cynthia Levy

Christopher L. Bowlus

Michael P. Manns

Xiaomin Lu

Gerald Crans

Chuhan Chung

G. Mani Subramanian

Robert P. Myers

Zachary Goodman

Naga Chalasani

John M. Vierling

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NEIL GUHA neil.guha@nottingham.ac.uk
Professor of Hepatology

Gideon M. Hirschfield



Abstract

Background & Aims
Serum alkaline phosphatase (ALP) and the enhanced liver fibrosis (ELF) score are used as endpoints in trials of patients with primary sclerosing cholangitis (PSC). We aimed to quantify inter- and intra-individual variation in levels of ALP and the ELF score over time, and evaluated their association with fibrosis progression.
Methods
We analyzed data from 234 patients with large-duct PSC enrolled in a 2-year, phase 2b placebo-controlled trial of simtuzumab. Participants were assessed by laboratory tests every 4 weeks, and liver biopsies collected at time of screening, week 48, and week 96.
Results
Serum levels of ALP and ELF scores did not differ significantly between simtuzumab and placebo groups, so the data were pooled. Median per-patient variations in ALP between clinic visits were approximately 12% over 12 weeks, 20% over 48 weeks, and 20% over 96 weeks. Reductions, unrelated to study intervention, of more than 40% in ALP were observed in 10.9% of patients with baseline activity greater than 2-fold the upper limit of normal (ULN) and 12.5% of patients with more than 3-fold the ULN at 1 year. At 2 years, reductions of more than 40% in ALP were observed in 15.8% of patients with baseline activity greater than 2-fold the ULN and 17.9% of patients with more than 3-fold the ULN. Among the 209 patients with Ishak fibrosis stage 0–4 at baseline, serum ALP activity did not associate with development of cirrhosis or with a 2-point increase in fibrosis stage at 2 years. In contrast, the median per-patient variation in ELF scores between clinic visits was approximately 3% over 12 weeks, 4% over 48 weeks, and 4% over 96 weeks. Elevated ELF scores at baseline and at weeks 12, 24 and 48, each associated with development of cirrhosis at 2 years (odds ratio >2.75; P < .01 for all timepoints). ELF scores at baseline and weeks 12, 24 and 48, also associated with a 2-point increase in fibrosis stage at 2 years (odds ratios all greater than 2; P < .01 for all timepoints).
Conclusions
In an analysis of data from patients with large-duct PSC enrolled in a prospective trial, we found large interindividual and intraindividual variations in serum ALP activity. Serum ALP activity did not associate with disease progression over a 2-year period. Variations in ELF score were smaller, and scores determined at multiple timepoints associated with fibrosis progression and development of cirrhosis.

Citation

Trivedi, P. J., Muir, A. J., Levy, C., Bowlus, C. L., Manns, M. P., Lu, X., …Hirschfield, G. M. (2021). Inter- and Intra-individual Variation, and Limited Prognostic Utility, of Serum Alkaline Phosphatase in a Trial of Patients With Primary Sclerosing Cholangitis. Clinical Gastroenterology and Hepatology, 19(6), 1248-1257. https://doi.org/10.1016/j.cgh.2020.07.032

Journal Article Type Article
Acceptance Date Jun 1, 2020
Online Publication Date Jul 21, 2020
Publication Date 2021-06
Deposit Date Jul 31, 2023
Journal Clinical Gastroenterology and Hepatology
Print ISSN 1542-3565
Electronic ISSN 1542-7714
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 19
Issue 6
Pages 1248-1257
DOI https://doi.org/10.1016/j.cgh.2020.07.032
Keywords Gastroenterology; Hepatology
Public URL https://nottingham-repository.worktribe.com/output/13755135
Publisher URL https://www.cghjournal.org/article/S1542-3565(20)30994-0/fulltext