SynthesisDigestive diseases and sciences2026
AI-Based Models for Risk Prediction in MASLD: A Systematic Review.
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.
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Who cites it
13 citing papers in PubMed.
- AI-Based Screening for At-Risk MASLD and Advanced Fibrosis in the US Population: A Cost-Effectiveness Analysis.Digestive diseases and sciences · 2026Article
- Artificial Intelligence, Real Results: AI Successfully Risk-Stratifies Patients with MASLD.Digestive diseases and sciences · 2026Article
- A conceptual agentic AI architecture for MASLD-associated significant fibrosis in primary care.PLOS digital health · 2026Article
- An Explainable AI Tool (FibroX) for Detecting Advanced Liver Fibrosis in Adults With Type 2 Diabetes: Protocol for a Pilot Crossover Trial.JMIR research protocols · 2026Article
- Article
- Commentary on Our Article, "Outcomes of Acute Pancreatitis in Lean Versus Non-lean MASLD Patients: A Nationwide Analysis.Digestive diseases and sciences · 2026Article
- Low Rates of MASLD Screening in Young Adults With Type 2 Diabetes: A Retrospective Cohort Study.Journal of the Endocrine Society · 2026Article
- Critical Insight into the Outcomes of Acute Pancreatitis in Lean Versus Non-lean Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) Patients: A Nationwide Analysis.Digestive diseases and sciences · 2026Article
- Comment on "Outcomes of Acute Pancreatitis in Lean Versus Non-lean Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) Patients: A Nationwide Analysis".Digestive diseases and sciences · 2026Article
- Ultrasound in cardiovascular care: a perspective on preventive, diagnostic, and monitoring applications.Frontiers in cardiovascular medicine · 2026Article
- A comprehensive narrative review of artificial intelligence use in the diagnosis and management of metabolic dysfunction-associated steatotic liver disease.Translational gastroenterology and hepatology · 2026Review
- Exposure-shaped immunometabolic networks in chronic liver disease: translating multi-omics and artificial intelligence into preventive biomarkers.Frontiers in immunology · 2026Review
- Multiorgan crosstalk in MASLD/MASH: from hepatic pathogenesis to systemic complications.Frontiers in endocrinology · 2025Review
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Authors and funding
9 authors.
Funding
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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.
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