Evidence map›Paper›PMID 41630082›Full record

ArticleEuropean journal of medical research2026

Interpretable machine learning reveals phosphorus-to-albumin ratio as a novel predictor of mortality and acute kidney injury in critically ill pancreatitis patients: a multi-center retrospective analysis.

Xuan Chen, Boying Liu, Gefei Wang

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Article in European journal of medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Xuan ChenDepartment of Gastroenterology, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China.
Boying LiuDepartment of Gastroenterology, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China. lbygdmc@163.com.
Gefei WangGuangdong Provincial Key Laboratory of Infectious Diseases and Molecular Immunopathology, Shantou University Medical College, Shantou, China. gefeiwang@stu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute kidney injury (AKI), a common and severe complication of acute pancreatitis (AP), is amenable to early intervention. Phosphorus-to-albumin ratio (PAR) is a novel composite biomarker unexplored in AP largely. Data of ICU patients with AP were extracted from MIMIC-IV database and eICU-CRD, respectively. PAR's link to prognosis and AKI in AP were analyzed via Kaplan-Meier curves, Cox regression, restricted cubic splines (RCS), and logistic regression. Subgroup analysis tested interactions. Key variables were identified using least absolute shrinkage and selection operator regression. AKI prediction models were built and evaluated via seven machine learning (ML) algorithms. Shapley additive explanations (SHAP) interpreted variable contributions. Survival analysis, Cox models, and RCS collectively demonstrated PAR, as a potential risk factor, is associated with 28-day and 1-year all-cause mortality in patients with AP. Logistic regression identified PAR as a risk factor for AKI development in AP. AKI-related clinical features including PAR were indentified. Seven ML models were constructed, among which the Light Gradient Boosting Machine (LightGBM) model achieved an area under receiver operating characteristic curve (AUROC) of 0.880 (95% CI 0.825-0.935) and area under precision-recall curve (AUPRC) of 0.944 in the test set, and an AUROC of 0.837 (95% CI 0.785-0.889) and AUPRC of 0.784 in the external validation set. SHAP analysis of the LightGBM model confirmed that higher PAR levels corresponded to a higher predicted probability of AKI. PAR is associated with prognosis and AKI of patients with AP. Integrating PAR with other key clinical features, our LightGBM model provides physicians with a streamlined and efficient tool for early AKI identification in high-risk AP patients.

Indexed as

Acute kidney injuryAcute pancreatitisMachine learningPhosphorus-to-albumin ratioPrediction modelPrognosis

Identifiers

PMID41630082
PMCPMC12879405

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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 Socratic graph.