ArticleScientific reports2025
Development and validation of a machine learning-based prediction model for hepatorenal syndrome in liver cirrhosis patients using MIMIC-IV and eICU databases.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.
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Who cites it
10 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Coagulation Risk Prediction in Patients With Liver Failure: Integrated Meta-Analysis and Machine Learning Model Study.JMIR medical informatics · 2025Pooled it
- Benchmarking imputation methods on real-world clinical time series with simulated spatio-temporal missingness.Nature communications · 2026Article
- Artificial intelligence in advanced liver disease: From risk stratification to decision.Journal of the Chinese Medical Association : JCMA · 2026Review
- A multicenter machine learning model for predicting ICU mortality in mechanically ventilated patients: development and external validation.BMC medical informatics and decision making · 2026Article
- Biomarker identification of triple negative breast cancer subtypes using machine learning.NPJ systems biology and applications · 2026Article
- Article
- Clinical diagnosis and biomarkers of acute kidney injury in liver cirrhosis: a systematic review.Therapeutic advances in gastroenterology · 2026Review
- The Kidney in the Shadow of Cirrhosis: A Critical Review of Renal Failure.Biomedicines · 2025Review
- Machine Learning-Based Prediction of Decompensation in Hepatitis B Virus-Related Cirrhosis.Diagnostics (Basel, Switzerland) · 2025Article
- Article
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5 authors.
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Abstract
Hepatorenal syndrome (HRS) is a key contributor to poor prognosis in liver cirrhosis. This study aims to leverage the database to build a predictive model for early identification of high-risk patients. From two sizable public databases, we retrieved pertinent information about the cirrhosis patients' therapies, comorbidities, laboratory results, and demographics. Patients from the eICU database served as a test set for external validation, while patients from the MIMIC database were divided into training and validation groups. Variables were screened using LASSO regression, Extreme Gradient Boosting (XG Boost), and Random Forest (RF). Core risk factors were determined from the intersection of the three methods. A predictive model was constructed using multivariable logistic regression and visualized via a nomogram. Model performance was assessed using ROC curves, decision curve analysis (DCA), clinical impact curves (CIC), and calibration curves. Eight critical variables associated with HRS were identified using machine learning methods. The final predictive model, based on five key variables-spontaneous bacterial peritonitis, red blood cell count, creatinine, activated partial thromboplastin time, and total bilirubin-showed excellent discrimination, with AUCs of 0.832 (95% CI 0.8069-0.8563) in the training set and 0.8415 (95% CI 0.8042-0.8789) in the validation set. The AUC in the external test set was 0.8212 (95% CI 0.7784-0.864). By integrating the MIMIC-IV database and machine learning algorithms, we developed an effective predictive model for HRS in liver cirrhosis patients, providing a robust tool for early clinical intervention.
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