Evidence map›Paper›PMID 38778481›Full record

ArticleAlimentary pharmacology & therapeutics2024

Liver function and portal-systemic shunting quantified by the oral cholate challenge test and risk for large oesophageal varices.

Tarek Hassanein, Andrew P Keaveny, Parvez Mantry, Alastair D Smith, Michael P McRae, John Kittelson, Steve Helmke, Gregory T Everson, SHUNT‐V Investigators

Abstract read
In one paragraph

Article in Alimentary pharmacology & therapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
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  4. Review
  5. Article
  6. Article
  7. Observational
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Tarek HassaneinSouthern California Research Center, Coronado, California, USA.
Andrew P KeavenyMayo Clinic, Jacksonville, Florida, USA.ORCID 0000-0003-2355-2433
Parvez MantryThe Liver Institute at Methodist Dallas Medical Center, Dallas, Texas, USA.
Alastair D SmithSyneos Health, Morrisville, North Carolina, USA.
Michael P McRaeCustom DX Solutions LLC, Houston, Texas, USA.ORCID 0000-0002-2126-9442
John KittelsonConsultant to HepQuant LLC, Denver, Colorado, USA.
Steve HelmkeHepQuant LLC, Denver, Colorado, USA.
Gregory T EversonHepQuant LLC, Denver, Colorado, USA.ORCID 0000-0003-0454-3566
SHUNT‐V Investigators

Funding

ZOVIRAX CREAM TO TREAT HERPES LABIALIS IN ADOLESCENTSM01RR000827 · NCRR · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAAS, RICHARD H · 1985 to 2010
$74.3M
ZOPOLRESTAT PHARMACOKINETICS IN DIABETICS WITH VARYING RENAL FUNCTIONM01RR000051 · NCRR · UNIVERSITY OF COLORADO DENVER · PI ALBERT, RICHARD K · 1985 to 2008
$52.6M
X-LINKED HYPOPHOSPHATEMIAM01RR000065 · NCRR · VIRGINIA COMMONWEALTH UNIVERSITY · PI NESTLER, JOHN E · 1985 to 2010
$24.8M
ROLE OF TRH IN THE PITUITARY AND CNSK04DK000827 · NIDDK · UNIVERSITY OF ROCHESTER · PI HINKLE, PATRICIA M. · 1986 to 1986
–
Hoffmann-La Roche, Inc.National Center on Minority Health and Health DisparitiesNational Institute of Allergy and Infectious DiseasesNCI NIH HHSNCRR NIH HHS M01 RR000051NCRR NIH HHS M01 RR000065NCRR NIH HHS M01 RR000827NIDDK NIH HHS M01RR-00051NIDDK NIH HHS M01RR-00065NIDDK NIH HHS M01RR-00827NIH General Clinical Research Centers
6 · The paper itself

Abstract

backgroundThe quantitative HepQuant SHUNT test of liver function and physiology generates a disease severity index (DSI) that correlates with risk for clinical complications, such as large oesophageal varices (LEVs). A derivative test, HepQuant DuO, generates an equivalent DSI and simplifies testing by requiring only oral administration of the test solution and two blood samples at 20 and 60 min.

aimsSince the DSIs measured from DuO and SHUNT are equivalent, we compared the diagnostic performance for large oesophageal varices (LEVs) between the DSIs measured from DuO and SHUNT tests.

methodsThis study combined the data from two prospectively conducted US studies: HALT-C and SHUNT-V. A total of 455 subjects underwent both the SHUNT test and esophagogastroduodenoscopy (EGD).

resultsDSI scores correlated with the probability of LEVs (p < 0.001) and demonstrated a stepwise increase from healthy lean controls without liver disease to subjects with chronic liver disease and no, small or large varices. Furthermore, a cutoff of DSI ≤ 18.3 from DuO had a sensitivity of 0.98 (missing only one case) and, if applied to the endoscopy (EGD) decision, would have prevented 188 EGDs (41.3%). The AUROC for DSI from DuO did not differ from that of the reference SHUNT test method (0.82 versus 0.81, p = 0.3500).

conclusionsDSI from HepQuant DuO links liver function and physiology to the risk of LEVs across a wide spectrum of patient characteristics, disease aetiologies and liver disease severity. DuO is minimally invasive, easy to administer, quantitative and may aid the decision to avoid or perform EGD for LEVs.

Indexed as

Esophageal and Gastric VaricesLiver Function TestsSeverity of Illness IndexAdultAgedEndoscopy, Digestive SystemFemaleHumansLiverMaleMiddle AgedProspective StudiesRisk Factors

Identifiers

PMID38778481
PMCPMC11348877

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Registered trials

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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.