A data-driven approach to decode metabolic dysfunction-associated steatotic liver disease.

Artificial intelligence Big data MASLD Machine learning NAFLD Precision medicine

Journal

Annals of hepatology
ISSN: 1665-2681
Titre abrégé: Ann Hepatol
Pays: Mexico
ID NLM: 101155885

Informations de publication

Date de publication:
20 Dec 2023
Historique:
received: 30 11 2023
accepted: 04 12 2023
medline: 23 12 2023
pubmed: 23 12 2023
entrez: 22 12 2023
Statut: aheadofprint

Résumé

Metabolic dysfunction-associated steatotic liver disease (MASLD), defined by the presence of liver steatosis together with at least one out of five cardiometabolic factors, is the most common cause of chronic liver disease worldwide, affecting around one in three people. Yet the clinical presentation of MASLD and the risk of progression to cirrhosis and adverse clinical outcomes is highly variable. It therefore represents both a global public health threat and a precision medicine challenge. The use of artificial intelligence (AI) is being investigated in MASLD to develop reproducible, quantitative, and automated methods to enhance patient stratification and to discover new biomarkers and therapeutic targets in MASLD. This review details the different applications of AI and machine learning algorithms in MASLD, particularly in the context of analyzing electronic health record, digital pathology, and imaging data. Additionally, it also describes how specific MASLD consortia are leveraging multimodal data sources to spark research breakthroughs in the field. Using a new national level 'data commons' (SteatoSITE) as an exemplar, the opportunities as well as the technical challenges of large-scale databases in MASLD research are highlighted.

Identifiants

pubmed: 38135251
pii: S1665-2681(23)00381-2
doi: 10.1016/j.aohep.2023.101278
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

101278

Informations de copyright

Copyright © 2023. Published by Elsevier España, S.L.U.

Déclaration de conflit d'intérêts

Conflicts of interest T.J.K. serves as a consultant for or has received speakers’ fees from Resolution Therapeutics, Clinnovate Health, Perspectum, Servier Laboratories, Kynos Therapeutics, and Incyte Corporation. J.A.F. serves as a consultant or advisory board member for Resolution Therapeutics, Kynos Therapeutics, Sosei Heptares, Ipsen, Redx Pharma, River 2 Renal Corp., Stimuliver, Galecto Biotech, Global Clinical Trial Partners and Guidepoint and has received research grant funding from Intercept Pharmaceuticals and Genentech. I.D. is a shareholder in Bering Limited.

Auteurs

Maria Jimenez-Ramos (M)

Centre for Inflammation Research, Institute for Regeneration and Repair, University of Edinburgh, Edinburgh BioQuarter, 4-5 Little France Drive, Edinburgh, EH16 4UU, UK.

Timothy J Kendall (TJ)

Centre for Inflammation Research, Institute for Regeneration and Repair, University of Edinburgh, Edinburgh BioQuarter, 4-5 Little France Drive, Edinburgh, EH16 4UU, UK; Edinburgh Pathology, University of Edinburgh, 51 Little France Crescent, Old Dalkeith Rd, Edinburgh, EH16 4SA, UK.

Ignat Drozdov (I)

Bering Limited, 54 Portland Place, London, W1B 1DY, London, UK.

Jonathan A Fallowfield (JA)

Centre for Inflammation Research, Institute for Regeneration and Repair, University of Edinburgh, Edinburgh BioQuarter, 4-5 Little France Drive, Edinburgh, EH16 4UU, UK. Electronic address: Jonathan.Fallowfield@ed.ac.uk.

Classifications MeSH