Evidence map›Paper›PMID 42293780›Full record

ReviewGastro hep advances2026

Evidence Supporting Utility of the Oral Cholate Challenge Test of Liver Function and Physiology to Aid Clinical Management: A Review of Analytical and Clinical Validation Studies.

Andrew P Keaveny, Kamran Qureshi, Mitchell Shiffman, Timothy R Morgan, K Rajender Reddy, Joanne C Imperial, Michael P McRae, Touraj Shokati, Gregory T Everson

Abstract readReview
In one paragraph

Review in Gastro hep advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Andrew P KeavenyDivision Gastroenterology and Hepatology, Mayo Clinic, Jacksonville, Florida.
Kamran QureshiDivision of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St. Louis, Missouri.
Mitchell ShiffmanBon Secours Liver Institute of Virginia, Richmond, Virginia.
Timothy R MorganDivision of Gastroenterology, University of California, Irvine, Irvine, California.
K Rajender ReddyDivision of Gastroenterology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.
Joanne C ImperialHepQuant, LLC, Denver, Colorado.
Michael P McRaeCustom DX Solutions LLC, Houston, Texas.
Touraj ShokatiHepQuant, LLC, Denver, Colorado.
Gregory T EversonHepQuant, LLC, Denver, Colorado.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current standard liver assessments rely on static laboratory values that reflect advanced disease or liver injury rather than overall hepatic health. This limitation highlights the need for dynamic measures of liver function to support accurate risk stratification, therapeutic monitoring, and clinical trial design. Quantitative liver function tests address this gap by providing physiologically based measures of hepatic clearance. Among these, cholate clearance is uniquely suited to assess hepatocellular function and portal-systemic shunting-key determinants of disease severity and prognosis. The oral cholate challenge test (OCCT), HepQuant DuO, is a simple, noninvasive method for quantifying cholate clearance using stable isotope-labeled cholate and liquid chromatography-tandem mass spectrometry analysis. This review highlights the test's analytical and clinical validation across the spectrum of chronic liver disease. The test's output parameters, Disease Severity Index, SHUNT%, and hepatic reserve, correlate with portal hypertension, varices, and risk for clinical outcomes. Applications for guiding endoscopic screening, predicting decompensation, and monitoring treatment response are highlighted. Comparative analyses show that the OCCT parameters outperform conventional laboratory tests of liver function and may complement anatomic or physical measurements, such as histology, magnetic resonance imaging, or elastography. Additional data supports its role as a sensitive biomarker and reasonably likely surrogate endpoint for drug trials of chronic liver disease. The OCCT addresses critical gaps in chronic liver disease and drug development and has the potential to transform the assessment of the patient with chronic liver disease.

Indexed as

CholateClinical OutcomesClinical TrialsLiver FunctionPortal HypertensionVarices

Identifiers

PMID42293780
PMCPMC13260197

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.