Evidence map›Paper›PMID 42467999›Full record

ReviewHepatology communications2026

The role of ammonia in chronic liver disease.

Annarein J C Kerbert, Maria Pilar Ballester, Christopher F Rose, Rajiv Jalan

Abstract readReview
In one paragraph

Review in Hepatology communications, 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

4 authors.

Annarein J C KerbertDepartment of Gastroenterology and Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
Maria Pilar BallesterDigestive Disease Department, Hospital Clínico Universitario de Valencia, Spain.
Christopher F RoseHepato-Neuro Laboratory, CRCHUM, Université de Montréal, Montreal, Quebec, Canada.
Rajiv JalanInstitute for Liver and Disease Health, University College London, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatic encephalopathy (HE) is a major neuropsychiatric complication of chronic liver disease that contributes substantially to morbidity, mortality, and healthcare burden. Ammonia, a neurotoxic metabolite, plays a central role in its pathogenesis. Although traditionally considered a byproduct of liver failure, growing evidence supports a more direct and causal role for ammonia, linking it not only to the clinical features of HE but also to key processes involved in disease progression, including liver injury, inflammation, immune dysfunction, muscle wasting, and impaired cellular energetics. Beyond its mechanistic implications, renewed interest has focused on ammonia as a clinically useful biomarker. Advances in risk stratification, dynamic testing, and longitudinal monitoring are improving the ability to use ammonia levels to identify patients at high risk of HE, predict clinical outcomes, and assess response to therapy. At the same time, emerging ammonia-lowering therapies are reshaping the treatment landscape. Whether these therapies may modify disease trajectory, beyond reversing HE, is an interesting hypothesis requiring validation in future studies. This review summarises current knowledge on ammonia metabolism, its role in the pathophysiology of HE and chronic liver disease, and its evolving clinical utility. By integrating molecular mechanisms with advances in measurement and treatment, we propose a reframing of ammonia as a central driver of liver-brain axis dysfunction and a meaningful target for precision-based therapeutic strategies.

Indexed as

AmmoniaHepatic EncephalopathyLiver DiseasesBiomarkersChronic DiseaseDisease ProgressionHumansAmmoniaBiomarkersbiomarkercirrhosisneurotoxicityrisk stratificationtherapeutic target

Identifiers

PMID42467999
PMCPMC13671592

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.