Evidence map›Paper›PMID 42399867›Full record

ReviewBMC medical informatics and decision making2026

Explainable AI machine learning framework for chronic kidney disease prediction utilizing electronic health records.

Muhammad Rizwan, Rashid Naseem, Muhammad Ahmad Khan, Arshad Ahmad, Muhammad Fozan, Nazeer Muhammad

Abstract readReviewValidation Study
In one paragraph

Review in BMC medical informatics and decision making, 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
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

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

6 authors.

Muhammad Rizwan *School of Computing Sciences, Pak-Austria Fachhochschule: Institute of Applied Sciences and Technology, Mang, Haripur, Khyber Pakhtunkhwa, 22600, Pakistan.ORCID 0009-0004-9735-1743
Rashid Naseem *School of Computing Sciences, Pak-Austria Fachhochschule: Institute of Applied Sciences and Technology, Mang, Haripur, Khyber Pakhtunkhwa, 22600, Pakistan.ORCID 0000-0002-4952-8100
Muhammad Ahmad KhanSchool of Computing Sciences, Pak-Austria Fachhochschule: Institute of Applied Sciences and Technology, Mang, Haripur, Khyber Pakhtunkhwa, 22600, Pakistan.ORCID 0000-0002-3307-8352
Arshad AhmadFaculty of Computing and IT, Sohar University, P.O. Box 311, Sohar, Oman.ORCID 0000-0002-3576-8365
Muhammad FozanDepartment of Biological and Health Sciences, Pak-Austria Fachhochschule: Institute of Applied Sciences and Technology, Mang, Haripur, Khyber PakhtunkhwaState, 22600, Pakistan.ORCID 0009-0004-1645-4127
Nazeer MuhammadCollege of Computer and Systems Engineering, Program for Data Science and AI, Abdullah Al Salem University, Khaldiya, Kuwait. nazeer.muhammad@aasu.edu.kw.ORCID 0000-0002-4056-9854

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic Kidney Disease (CKD) is one of the significant health issues in the world which is usually unnoticeable and afterwards causes greater morbidity and mortality. Timely intervention is important in early diagnosis that will enhance patient outcomes.

methodsThis study proposes an explainable artificial intelligence driven machine learning (ML) framework for CKD prediction using electronic health records. A dataset of 398 patients (241 CKD and 157 non-CKD) from Pakistan Kidney Center, Abbottabad, was analyzed using multiple models, including logistic regression, decision tree, k-nearest neighbors, gradient boosting, CatBoost, AdaBoost, XGBoost, and random forest (RF). Feature selection methods mutual information, DT, and RF identified the most informative clinical variables, and experiments were conducted using both full and top 10 feature subsets. Model performance was evaluated using stratified 5-fold and 10-fold cross-validation with metrics such as accuracy, precision, recall, F1-score, balanced accuracy, MCC, and AUC. Statistical validation was performed using confidence intervals, McNemar's test, ANOVA, and Tukey HSD. Model interpretability was achieved using Hapley Additive exPlanations (SHAP) and Local Interpretable Model-agnostic Explanations (LIME).

resultsThe results demonstrated consistently high performance across all models, with the RF model achieving an accuracy of 98%. Statistical analysis revealed no significant differences among top-performing models, indicating comparable predictive capabilities. Feature-level analysis identified key biomarkers-estimated glomerular filtration rate, creatinine, and urea-as having large effect sizes and strong discriminative power. The reduced feature set maintained competitive performance, highlighting the efficiency of selected variables. Model interpretability using SHAP and LIME provided transparent and clinically meaningful insights, confirming the importance of these features in CKD prediction.

conclusionThe proposed framework demonstrates robust and reliable performance for CKD prediction, supported by comprehensive statistical validation and explainability analysis. The findings indicate that predictive performance is primarily driven by the strength of selected clinical features, enabling multiple ML models to achieve comparable results. This approach offers a practical, interpretable, and generalizable solution for early CKD detection in clinical settings.

Indexed as

Electronic Health RecordsMachine LearningPredictive Learning ModelsRenal Insufficiency, ChronicBiomarkersCreatinineEarly DiagnosisFemaleGlomerular Filtration RateHumansMalePakistanPrediction AlgorithmsRandom ForestRisk AssessmentUreaBiomarkersCreatinineUreaChronic kidney diseaseElectronic health recordsEXplainable artificial intelligenceMachine learningRandom forest

Identifiers

PMID42399867
PMCPMC13340084

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.