Artificial intelligence for metabolic dysfunction-associated steatotic liver disease diagnosis: A systematic review
Clinical Snapshot
PICO Framework
| P — Population | Patients with metabolic dysfunction-associated steatotic liver disease (MASLD) requiring diagnosis |
| I — Intervention | Artificial intelligence applications (deep learning, machine learning models) for diagnostic purposes |
| C — Comparator | Traditional diagnostic methods, expert interpretation, or standard clinical assessment |
| O — Outcomes | Diagnostic accuracy, sensitivity, specificity, automated steatosis quantification, fibrosis staging performance |
Bottom Line
This systematic review examines AI applications for diagnosing metabolic dysfunction-associated steatotic liver disease, including 191 studies from 2020-2026. The authors report that AI models demonstrate high diagnostic performance across ultrasound, CT, and MRI imaging, with accuracy comparable to expert interpretation for steatosis quantification and fibrosis staging. AI integration with multi-omics data shows promise for biomarker discovery and therapeutic targeting. However, significant limitations remain including model generalisability, lack of standardization, and clinical integration challenges. The evidence quality assessment is limited by insufficient methodological details, absence of quantitative synthesis, and no formal quality appraisal of included studies. While AI shows substantial potential to transform MASLD diagnostics, the authors appropriately conclude that prospective validation and implementation strategies are essential before widespread clinical adoption. Clinicians should await further validation studies and regulatory approval before incorporating these technologies into routine practice.
Key Findings
P Value: Not reported
Effect Size: Not quantified - described as 'high diagnostic performance'
Primary Outcome: Diagnostic performance of AI models for MASLD across multiple imaging modalities
Nnt Or Sensitivity: Accuracy described as 'comparable to expert interpretation' but specific sensitivity/specificity values not provided
Confidence Interval: Not reported
Clinical Application
Limited by current challenges in model generalisability, standardization, and clinical integration as identified by authors Relevant to Australian practice given MASLD prevalence, but TGA approval and PBS considerations for AI diagnostic tools would be required. Integration with existing imaging infrastructure and RACGP guidelines for liver disease screening would need consideration Patients requiring MASLD diagnosis across primary care and specialist hepatology settings
Abstract
Metabolic dysfunction-associated steatotic liver disease (MASLD) poses significant diagnostic challenges. We conducted a systematic review of artificial intelligence (AI) applications in MASLD diagnosis, focusing on predictive modeling, screening, imaging analysis, and therapeutic assistance. Following PRISMA guidelines, we searched five databases (Web of Science, SciFinder, Elsevier ScienceDirect, EBSCOhost, Springer) for studies published January 2020-January 2026. Of 1247 initially identified records, 191 studies met inclusion criteria. AI models demonstrate high diagnostic performance across multiple modalities. Deep learning analysis of US, CT, and MRI enables automated steatosis quantification and fibrosis staging with accuracy comparable to expert interpretation. AI integration with multi-omics data facilitates novel biomarker discovery and therapeutic target identification. Despite these advances, model generalisability, standardization, and clinical integration remain challenges. AI holds substantial potential to transform MASLD diagnostics, but prospective validation and implementation strategies are needed before widespread clinical adoption.
References
- 1.Wang, R., Liu, C., Xue, M., Qian, J., & Hu, Y. (2026). Artificial intelligence for metabolic dysfunction-associated steatotic liver disease diagnosis: A systematic review. Computers in Biology and Medicine, 111619. https://doi.org/10.1016/j.compbiomed.2026.111619
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