Evidence map›Paper›PMID 41231418›Full record

SynthesisDigestive diseases and sciences2026

AI-Based Models for Risk Prediction in MASLD: A Systematic Review.

Basile Njei, Yazan A Al-Ajlouni, Samira Yaya Lemos, Derek Ugwendum, Nelvis Njei, Omar Al Ta'ani, Prince Ameyaw, Lea-Pearl Njei, Sarpong Boateng

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Digestive diseases and sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
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.

Basile NjeiInternational Medicine Program (Section of Digestive Diseases), Yale School of Medicine, Yale University, New Haven, CT, USA. basile.njei@yale.edu.
Yazan A Al-AjlouniMontefiore Medical Center, Bronx, NY, USA.
Samira Yaya LemosYaoundé General Hospital, Yaoundé, Cameroon.
Derek UgwendumRichmond University Medical Center, Staten Island, New York, USA.
Nelvis NjeiCenters for Medicare and Medicaid Services, Baltimore, MD, USA.
Omar Al Ta'aniDepartment of Internal Medicine, Allegheny Health Network, Pittsburgh, PA, USA.
Prince AmeyawYale Affiliated Hospitals Program, Bridgeport, CT, USA.
Lea-Pearl NjeiUniversity of Maryland Baltimore County, Baltimore, MD, USA.
Sarpong BoatengCenters for Medicare and Medicaid Services, Baltimore, MD, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetabolic dysfunction-associated steatotic liver disease (MASLD) is a rapidly growing global health concern. This systematic review evaluates the efficacy of AI-based models in predicting risk and stratifying patients with MASLD, with a focus on identifying individuals at risk for clinically significant disease, such as ≥ F2 fibrosis, ≥ F3 advanced fibrosis, or MASH, addressing a critical gap in the literature to enhance clinical management and patient outcomes.

methodsFollowing PRISMA guidelines, we conducted a comprehensive literature search across PubMed, MEDLINE, Web of Science, EMBASE, and CINAHL on November 19, 2024 and June 9, 2025. Predefined keywords were used to identify relevant studies focused on AI-based risk prediction for MASLD. Inclusion and exclusion criteria were established, and data were extracted using a structured form, emphasizing AI model efficacy and quality assessment via the QUADAS-2 tool. This study is registered in the PROSPERO database (CRD42024606950) and conducted without external funding.

resultsWe included 26 studies (2014-2025) from Europe, the U.S.A., Asia, and South America spanning retrospective cohorts and cross-sectional designs. Risk of bias (QUADAS-2) was predominantly low overall: patient selection and index test were low risk in all studies; flow/timing was uniformly low risk; reference standard was low risk in most studies with a minority rated unclear. Performance by endpoint (validation/test cohorts): AI models for MASH reported AUROCs of ~ 0.76-0.95 (with external validation AUROCs as low as 0.67), while models for fibrosis ≥ F2-F4 reported AUROCs of ~ 0.72-0.94. Models leveraged machine learning and deep learning approaches; key predictors frequently included age, BMI, liver enzymes (ALT/AST ± GGT), platelets, and other routine clinical features, with multimodal (clinical ± elastography/imaging) inputs often yielding the strongest discrimination within study contexts.

conclusionThis review highlights the promising role of AI-based models in MASLD risk prediction, showcasing their strong predictive capabilities. Addressing limitations in data diversity and model interpretability will be crucial for integrating AI into clinical practice.

Indexed as

Artificial IntelligenceFatty LiverHumansPredictive Value of TestsRisk AssessmentRisk FactorsAI-based risk predictionDeep learning in healthcareMachine learning in liver diseaseMetabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)Noninvasive diagnostic models

Identifiers

What OpenQuestion 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 OpenQuestion graph.