Research Appraisalother

AI in the Prediction of Hepatic Fibrosis Progression Using Non-Coding RNAs

Clinica chimica acta; international journal of clinical chemistryRoy, Dibakar, Hussain, Md Sadique, Khan, Yumna et al.15 May 2026DOI

Clinical Snapshot

20CEBM
Evidence: Insufficientother

PICO Framework

P — PopulationPatients with hepatic fibrosis or at risk of fibrosis progression
I — InterventionAI-based analysis of non-coding RNAs (miRNAs, lncRNAs, circRNAs)
C — ComparatorTraditional biopsy techniques and conventional biomarkers
O — OutcomesPrediction of fibrosis progression, disease staging, and prognosis

Bottom Line

This narrative review explores the potential of combining artificial intelligence with non-coding RNA analysis to predict hepatic fibrosis progression. While the concept is scientifically interesting and addresses the important clinical need for non-invasive fibrosis assessment, this review lacks the systematic methodology required for evidence-based practice recommendations. The authors appropriately acknowledge that standardization and clinical validation are still needed. Current evidence is insufficient to support routine clinical implementation. Australian clinicians should await properly designed validation studies and regulatory approval before considering these approaches. Traditional non-invasive fibrosis assessment tools (FIB-4, APRI, elastography) remain the standard of care until robust clinical evidence emerges for AI-enhanced ncRNA biomarkers.

Evidence: Insufficient

Key Findings

  • Effect Size: Not quantified - narrative synthesis only

  • Primary Outcome: Potential of AI-enhanced ncRNA analysis for hepatic fibrosis prediction

  • Nnt Or Sensitivity: Diagnostic accuracy metrics not systematically reported

  • Confidence Interval: Not provided

Clinical Application

Currently limited - requires specialized laboratory capabilities and validation studies Would require TGA approval for diagnostic applications; not currently covered by PBS; needs validation in Australian populations before RACGP guideline consideration Patients with chronic liver disease at risk of fibrosis progression

Abstract

Hepatic fibrosis is a dynamic and progressive condition that can lead to cirrhosis and hepatocellular carcinoma (HCC) if left untreated. Appropriate assessment of the disease progression of fibrosis is critical for early intervention and individualized treatment regimens. Traditional biopsy techniques are invasive and prone to sampling errors, highlighting the need for less invasive predictive techniques. Non-coding RNAs (ncRNAs), including microRNAs (miRNAs), long ncRNAs (lncRNAs), and circular RNAs (circRNAs), have emerged as key regulators of hepatic fibrogenesis and as a possible biomarker for disease staging and prognosis. The emergence of artificial intelligence (AI), particularly machine learning (ML) and deep learning (DL), has revolutionized the comprehensive large-scale analysis of transcriptomic data, enhancing the identification of ncRNA biomarkers and predictive modeling. The AI-based algorithms have been found to be more precise in anticipating fibrosis progression by means of integrating multi-omics data, ncRNA interaction networks, and by improving non-invasive diagnostic tools. This review involves the analysis of AI and ncRNA research in hepatic fibrosis, highlighting recent discoveries, possible challenges, and future opportunities. We address the necessity of standardization of data and clinical validation, as well as discuss the role of AI in identifying biomarkers of ncRNA, predicting the stage of fibrosis and risk stratification. ncRNA analysis with AI has a tremendous potential of transforming the diagnostics and prognostics of hepatic fibrosis, enabling precision hepatology.

References

  1. 1.Roy, D., Hussain, M. S., Khan, Y., Patel, D. N., Smerat, A., Bainsal, N., Ashique, S., Kumar, A., Khan, I. A., Dilorom, O., Allaberganova, M., & Ashirova, A. (2026). AI in the prediction of hepatic fibrosis progression using non-coding RNAs. Clinica Chimica Acta, 120973. https://doi.org/10.1016/j.cca.2026.120973
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