Machine Learning Identifies Metabolic Dysfunction–Associated Steatotic Liver Disease in Patients With Diabetes Mellitus

Author:

Nabrdalik Katarzyna12ORCID,Kwiendacz Hanna1ORCID,Irlik Krzysztof23ORCID,Hendel Mirela3ORCID,Drożdż Karolina1ORCID,Wijata Agata M24ORCID,Nalepa Jakub25ORCID,Janota Oliwia1ORCID,Wójcik Wiktoria3,Gumprecht Janusz1ORCID,Lip Gregory Y H26

Affiliation:

1. Department of Internal Medicine, Diabetology and Nephrology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia , 40-055 Katowice , Poland

2. Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital , Liverpool L69 3BX , UK

3. Students’ Scientific Association by the Department of Internal Medicine, Diabetology and Nephrology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia , 40-055 Katowice , Poland

4. Faculty of Biomedical Engineering, Silesian University of Technology , 41-800 Zabrze , Poland

5. Department of Algorithmics and Software, Silesian University of Technology , 44-100 Gliwice , Poland

6. Danish Center for Health Services Research, Department of Clinical Medicine, Aalborg University , 9220 Aalborg , Denmark

Abstract

Abstract Context The presence of metabolic dysfunction–associated steatotic liver disease (MASLD) in patients with diabetes mellitus (DM) is associated with a high risk of cardiovascular disease, but is often underdiagnosed. Objective To develop machine learning (ML) models for risk assessment of MASLD occurrence in patients with DM. Methods Feature selection determined the discriminative parameters, utilized to classify DM patients as those with and without MASLD. The performance of the multiple logistic regression model was quantified by sensitivity, specificity, and percentage of correctly classified patients, and receiver operating characteristic (ROC) curve analysis. Decision curve analysis (DCA) assessed the model's net benefit for alternative treatments. Results We studied 2000 patients with DM (mean age 58.85 ± 17.37 years; 48% women). Eight parameters: age, body mass index, type of DM, alanine aminotransferase, aspartate aminotransferase, platelet count, hyperuricaemia, and treatment with metformin were identified as discriminative. The experiments for 1735 patients show that 744/991 (75.08%) and 586/744 (78.76%) patients with/without MASLD were correctly identified (sensitivity/specificity: 0.75/0.79). The area under ROC (AUC) was 0.84 (95% CI, 0.82-0.86), while DCA showed a higher clinical utility of the model, ranging from 30% to 84% threshold probability. Results for 265 test patients confirm the model's generalizability (sensitivity/specificity: 0.80/0.74; AUC: 0.81 [95% CI, 0.76-0.87]), whereas unsupervised clustering identified high-risk patients. Conclusion A ML approach demonstrated high performance in identifying MASLD in patients with DM. This approach may facilitate better risk stratification and cardiovascular risk prevention strategies for high-risk patients with DM at risk of MASLD.

Funder

Silesian University of Technology

Publisher

The Endocrine Society

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