Machine learning models are superior to noninvasive tests in identifying clinically significant stages of NAFLD and NAFLD‐related cirrhosis. Issue 2 (9th February 2023)
- Record Type:
- Journal Article
- Title:
- Machine learning models are superior to noninvasive tests in identifying clinically significant stages of NAFLD and NAFLD‐related cirrhosis. Issue 2 (9th February 2023)
- Main Title:
- Machine learning models are superior to noninvasive tests in identifying clinically significant stages of NAFLD and NAFLD‐related cirrhosis
- Authors:
- Chang, Devon
Truong, Emily
Mena, Edward A.
Pacheco, Fabiana
Wong, Micaela
Guindi, Maha
Todo, Tsuyoshi T.
Noureddin, Nabil
Ayoub, Walid
Yang, Ju Dong
Kim, Irene K.
Kohli, Anita
Alkhouri, Naim
Harrison, Stephen
Noureddin, Mazen - Abstract:
- Abstract : Background and Aims: We assessed the performance of machine learning (ML) models in identifying clinically significant NAFLD‐associated liver fibrosis and cirrhosis. Approach and Results: We implemented ML models including logistic regression (LR), random forest (RF), and artificial neural network to predict histological stages of fibrosis using 17 demographic/clinical features in 1370 patients with NAFLD who underwent liver biopsy, FibroScan, and labs within a 6‐month period at multiple U.S. centers. Histological stages of fibrosis (≥F2, ≥F3, and F4) were predicted using ML, FibroScan liver stiffness measurements, and Fibrosis‐4 index (FIB‐4). NASH with significant fibrosis (NAS ≥ 4 + ≥F2) was assessed using ML, FibroScan‐AST (FAST) score, FIB‐4, and NAFLD fibrosis score (NFS). We used 80% of the cohort to train and 20% to test the ML models. For ≥F2, ≥F3, F4, and NASH + NAS ≥ 4 + ≥F2, all ML models, especially RF, had primarily higher accuracy and AUC compared with FibroScan, FIB‐4, FAST, and NFS. AUC for RF versus FibroScan and FIB‐4 for ≥F2, ≥F3, and F4 were (0.86 vs. 0.81, 0.78), (0.89 vs. 0.83, 0.82), and (0.89 vs. 0.86, 0.85), respectively. AUC for RF versus FAST, FIB‐4, and NFS for NASH + NAS ≥ 4 + ≥F2 were (0.80 vs. 0.77, 0.66, 0.63). For NASH + NAS ≥ 4 + ≥F2, all ML models had lower/similar percentages within the indeterminate zone compared with FIB‐4 and NFS. Overall, ML models performed better in sensitivity, specificity, positive predictive value, andAbstract : Background and Aims: We assessed the performance of machine learning (ML) models in identifying clinically significant NAFLD‐associated liver fibrosis and cirrhosis. Approach and Results: We implemented ML models including logistic regression (LR), random forest (RF), and artificial neural network to predict histological stages of fibrosis using 17 demographic/clinical features in 1370 patients with NAFLD who underwent liver biopsy, FibroScan, and labs within a 6‐month period at multiple U.S. centers. Histological stages of fibrosis (≥F2, ≥F3, and F4) were predicted using ML, FibroScan liver stiffness measurements, and Fibrosis‐4 index (FIB‐4). NASH with significant fibrosis (NAS ≥ 4 + ≥F2) was assessed using ML, FibroScan‐AST (FAST) score, FIB‐4, and NAFLD fibrosis score (NFS). We used 80% of the cohort to train and 20% to test the ML models. For ≥F2, ≥F3, F4, and NASH + NAS ≥ 4 + ≥F2, all ML models, especially RF, had primarily higher accuracy and AUC compared with FibroScan, FIB‐4, FAST, and NFS. AUC for RF versus FibroScan and FIB‐4 for ≥F2, ≥F3, and F4 were (0.86 vs. 0.81, 0.78), (0.89 vs. 0.83, 0.82), and (0.89 vs. 0.86, 0.85), respectively. AUC for RF versus FAST, FIB‐4, and NFS for NASH + NAS ≥ 4 + ≥F2 were (0.80 vs. 0.77, 0.66, 0.63). For NASH + NAS ≥ 4 + ≥F2, all ML models had lower/similar percentages within the indeterminate zone compared with FIB‐4 and NFS. Overall, ML models performed better in sensitivity, specificity, positive predictive value, and negative predictive value compared with traditional noninvasive tests. Conclusions: ML models performed better overall than FibroScan, FIB‐4, FAST, and NFS. ML could be an effective tool for identifying clinically significant liver fibrosis and cirrhosis in patients with NAFLD. Abstract : … (more)
- Is Part Of:
- Hepatology. Volume 77:Issue 2(2023)
- Journal:
- Hepatology
- Issue:
- Volume 77:Issue 2(2023)
- Issue Display:
- Volume 77, Issue 2 (2023)
- Year:
- 2023
- Volume:
- 77
- Issue:
- 2
- Issue Sort Value:
- 2023-0077-0002-0000
- Page Start:
- 546
- Page End:
- 557
- Publication Date:
- 2023-02-09
- Subjects:
- Heart -- Diseases -- Nursing -- Periodicals
Lungs -- Diseases -- Nursing -- Periodicals
Intensive care nursing -- Periodicals
Foie -- Maladies -- Périodiques
616.362 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1527-3350 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/hep.32655 ↗
- Languages:
- English
- ISSNs:
- 0270-9139
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.836000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26804.xml