Evidence map›Paper›PMID 41098241›Full record

ReviewJHEP reports : innovation in hepatology2025

Non-invasive tests for MetALD and alcohol-related liver disease.

Stine Johansen, Maja Thiele, Aleksander Krag

Abstract readReview
In one paragraph

Review in JHEP reports : innovation in hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Steatosis liver index: A validated machine learning model using clinical data distinguishes steatotic liver disease phenotypes.Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver · 2026
    Article
  2. On the History of Hepatic Vein Catheterization.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Article
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

3 authors.

Stine JohansenFibrosis, Fatty Liver and Steatohepatitis Research Center Odense (FLASH), Department of Gastroenterology and Hepatology, Odense University Hospital, Odense, Denmark.
Maja ThieleFibrosis, Fatty Liver and Steatohepatitis Research Center Odense (FLASH), Department of Gastroenterology and Hepatology, Odense University Hospital, Odense, Denmark.
Aleksander KragFibrosis, Fatty Liver and Steatohepatitis Research Center Odense (FLASH), Department of Gastroenterology and Hepatology, Odense University Hospital, Odense, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic- and alcohol-related liver disease (MetALD) and alcohol-related liver disease (ALD) are major drivers of the global burden of cirrhosis. While metabolic dysfunction-associated steatotic liver disease (MASLD) affects nearly one-third of the global population, ALD and MetALD, though far less common, account for a disproportionately high rate of liver-related complications and deaths. Despite this, research and clinical focus on ALD and MetALD remain limited. A critical barrier is the late stage at which these conditions are typically diagnosed, often after the onset of decompensation. In this review, we explore the potential of non-invasive tests (NITs) to change the diagnostic landscape of ALD and MetALD. NITs offer a practical and scalable means to detect liver disease at earlier, compensated stages, before symptoms emerge, thereby opening a window for timely intervention. Beyond diagnosis, these tools also serve important roles in risk assessment, disease monitoring, and evaluating treatment response. As interest in therapeutic developments for ALD and MetALD grows, NITs are expected to become central to trial design, helping to identify suitable participants, assess ongoing alcohol use, and monitor efficacy without reliance on invasive biopsies. We also discuss broader strategies necessary to support early detection, including policy changes, stigma reduction, and improved access to care. Finally, we consider emerging biomarkers and their promise in advancing precision medicine approaches tailored to this high-risk patient population.

Indexed as

alcoholic liver diseaseBiomarkerdecompensationPEthprognosis

Identifiers

PMID41098241
PMCPMC12519246

What OpenQuestion holds

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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.