Evidence map›Paper›PMID 42015825›Full record

ArticleRenal failure2026

Explainable machine learning integrating bioelectrical impedance for 6-month cardiovascular risk in peritoneal dialysis.

Yi Liang Tsai, Chia Lin Wu, Jung Hsien Chiang

Abstract read
In one paragraph

Article in Renal failure, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Yi Liang TsaiDepartment of Medical Research, Renal Medicine Laboratory, Changhua Christian Hospital, Changhua, Taiwan.ORCID 0000-0002-3271-2358
Chia Lin WuDepartment of Medical Research, Renal Medicine Laboratory, Changhua Christian Hospital, Changhua, Taiwan.ORCID 0000-0001-6045-6956
Jung Hsien ChiangDepartment of Computer Science and Information Engineering, National Cheng Kung University, Tainan, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peritoneal dialysis (PD) is a common treatment for end-stage renal disease, yet cardiovascular disease (CVD) remains a major cause of morbidity. Inadequate fluid management can elevate CVD risk, and bioelectrical impedance spectroscopy (BIS) is increasingly used to assess fluid status. This study aimed to develop an artificial intelligence model integrating BIS measurements and medical history to predict major adverse cardiovascular events (MACEs) within six months in clinically stable PD patients. Data were stratified by MACE occurrence and subject, with 80% assigned to training and 20% to testing. Class imbalance was addressed using the synthetic minority over-sampling technique. Four algorithms - logistic regression, random forest, XGBoost, and deep neural networks - were trained using fivefold cross-validation and grid search for optimal hyperparameters. Model performance was evaluated with area under the ROC curve (AUC), calibration plots, and decision curve analysis (DCA). Feature ablation experiments compared models using all 15 features, only 11 BIS-recorded features, and only 4 medical history features. The random forest model achieved the highest performance (AUC = 0.88), with CVD history as the most influential predictor. Isotonic regression calibration improved probability alignment (brier score = 0.0451). DCA suggested potential clinical benefit. While the model relied on four medical history features, its initial sensitivity was modest (0.68). Integrating BIS features significantly enhanced diagnostic sensitivity (0.84). The random forest model, based on 15 clinically accessible features, accurately predicts the risk of MACE within six months in clinically stable PD patients, demonstrating strong discriminatory ability with a performance reaching 88%.

Indexed as

Cardiovascular DiseasesElectric ImpedanceKidney Failure, ChronicMachine LearningPeritoneal DialysisAgedBoosting Machine Learning AlgorithmsClassification AlgorithmsFemaleHumansLogistic ModelsMaleMiddle AgedPrediction AlgorithmsPredictive Learning ModelsRandom Forestbioelectrical impedance analysisfluid overloadmajor adverse cardiovascular eventsperitoneal dialysisRandom forestrisk prediction

Identifiers

PMID42015825
PMCPMC13103996

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.