Evidence map›Paper›PMID 42840265›Full record

ArticleFrontiers in digital health2026

Development of a machine learning model to identify individuals with VCTE-derived at-risk MASH in a Spanish Mediterranean region.

Marta Cedenilla, David Marti-Aguado, Josep Redon, Inma Sauri-Ferrer, Jorge Navarro, Desamparados Escudero, Anton Gomez, Luis Cea-Calvo, Carlos J Martos-Rodriguez, Javier Díaz Carnicero

Abstract read
In one paragraph

Article in Frontiers in digital health, 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
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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

10 authors.

Marta Cedenilla *Value & Implementation, Global Medical & Scientific Affairs, Merck Sharp & Dohme Spain, Madrid, Spain.
David Marti-Aguado *Data Science Platform Biomedical Research Institute, Valencia, Spain.
Josep RedonData Science Platform Biomedical Research Institute, Valencia, Spain.
Inma Sauri-FerrerData Science Platform Biomedical Research Institute, Valencia, Spain.
Jorge NavarroData Science Platform Biomedical Research Institute, Valencia, Spain.
Desamparados EscuderoData Science Platform Biomedical Research Institute, Valencia, Spain.
Anton GomezValue & Implementation, Global Medical & Scientific Affairs, Merck Sharp & Dohme Spain, Madrid, Spain.
Luis Cea-CalvoValue & Implementation, Global Medical & Scientific Affairs, Merck Sharp & Dohme Spain, Madrid, Spain.
Carlos J Martos-RodriguezValue & Implementation, Global Medical & Scientific Affairs, Merck Sharp & Dohme Spain, Madrid, Spain.
Javier Díaz CarniceroData Science Platform Biomedical Research Institute, Valencia, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: While current guidelines recommend screening for liver disease in target populations, existing non-invasive tests have limitations in identifying at-risk metabolic dysfunction-associated steatohepatitis (MASH). Materials and methods: This retrospective study used two large datasets from the general population in the Valencian Community region (Spain). The primary goal was to develop a machine learning model to identify individuals with at-risk MASH. The model was constructed using a well-characterized dataset ( Results: In the independent validation dataset, VARM-7 exhibited a significantly higher AUROC compared with Fibrosis-4 (FIB-4) for identifying at-risk MASH (0.84 Conclusion: VARM-7 showed strong performance in identifying individuals with a VCTE-derived at-risk MASH. Our model could improve disease screening and referral pathways, but external validation and prognostic evaluation are needed before its implementation.

Indexed as

artificial intelligencemachine learningmetabolic dysfunction-associated steatohepatitismetabolic dysfunction–associated steatotic liver diseasenon-invasive test

Identifiers

PMID42840265
PMCPMC13638652

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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.