Artificial intelligence applied to omics data in liver diseases: Enhancing clinical predictions.

artificial intelligence clinical outcome prediction liver disease machine learning omics data

Journal

Frontiers in artificial intelligence
ISSN: 2624-8212
Titre abrégé: Front Artif Intell
Pays: Switzerland
ID NLM: 101770551

Informations de publication

Date de publication:
2022
Historique:
received: 21 09 2022
accepted: 31 10 2022
entrez: 2 12 2022
pubmed: 3 12 2022
medline: 3 12 2022
Statut: epublish

Résumé

Rapid development of biotechnology has led to the generation of vast amounts of multi-omics data, necessitating the advancement of bioinformatics and artificial intelligence to enable computational modeling to diagnose and predict clinical outcome. Both conventional machine learning and new deep learning algorithms screen existing data unbiasedly to uncover patterns and create models that can be valuable in informing clinical decisions. We summarized published literature on the use of AI models trained on omics datasets, with and without clinical data, to diagnose, risk-stratify, and predict survivability of patients with non-malignant liver diseases. A total of 20 different models were tested in selected studies. Generally, the addition of omics data to regular clinical parameters or individual biomarkers improved the AI model performance. For instance, using NAFLD fibrosis score to distinguish F0-F2 from F3-F4 fibrotic stages, the area under the curve (AUC) was 0.87. When integrating metabolomic data by a GMLVQ model, the AUC drastically improved to 0.99. The use of RF on multi-omics and clinical data in another study to predict progression of NAFLD to NASH resulted in an AUC of 0.84, compared to 0.82 when using clinical data only. A comparison of RF, SVM and kNN models on genomics data to classify immune tolerant phase in chronic hepatitis B resulted in AUC of 0.8793-0.8838 compared to 0.6759-0.7276 when using various serum biomarkers. Overall, the integration of omics was shown to improve prediction performance compared to models built only on clinical parameters, indicating a potential use for personalized medicine in clinical setting.

Identifiants

pubmed: 36458100
doi: 10.3389/frai.2022.1050439
pmc: PMC9705954
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

1050439

Informations de copyright

Copyright © 2022 Baciu, Xu, Alim, Prayitno and Bhat.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Cristina Baciu (C)

Ajmera Transplant Program, University Health Network, Toronto, ON, Canada.

Cherry Xu (C)

Ajmera Transplant Program, University Health Network, Toronto, ON, Canada.
Faculty of Health Sciences, McMaster University, Hamilton, ON, Canada.

Mouaid Alim (M)

Ajmera Transplant Program, University Health Network, Toronto, ON, Canada.
Departments of Computer Science and Cell and System Biology, University of Toronto, Toronto, ON, Canada.

Khairunnadiya Prayitno (K)

Ajmera Transplant Program, University Health Network, Toronto, ON, Canada.

Mamatha Bhat (M)

Ajmera Transplant Program, University Health Network, Toronto, ON, Canada.
Division of Gastroenterology and Hepatology, University Health Network and University of Toronto, Toronto, ON, Canada.
Toronto General Research Institute, University Health Network, Toronto, ON, Canada.

Classifications MeSH