Evidence map›Paper›PMID 42572776›Full record

ArticleJournal of inflammation research2026

A Host-Clinical Integrated Prediction Model for Early Sepsis Risk in Diabetic Patients with Acute Infections: Development and Internal Validation.

Xilong Pan, Zhiyuan Xu, ChanJuan Zhuo, Li Chen

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Article in Journal of inflammation 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xilong PanDepartment of Clinical Laboratory, Dongsheng Hospital, Zhongshan, Guangdong, People's Republic of China.ORCID 0000-0001-7195-8249
Zhiyuan XuDepartment of Critical Care Medicine, Dongsheng Hospital, Zhongshan, Guangdong, People's Republic of China.
ChanJuan ZhuoDepartment of Clinical Laboratory, Dongsheng Hospital, Zhongshan, Guangdong, People's Republic of China.
Li ChenDepartment of Clinical Laboratory, Dongsheng Hospital, Zhongshan, Guangdong, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Diabetic patients exhibit increased susceptibility to infections and a higher risk of progression to sepsis. This study aimed to develop a sepsis risk prediction model specifically for diabetic patients with acute infections. Methods: In this retrospective, single-center study, we enrolled 604 hospitalized diabetic patients with acute infections. A propensity score-matched cohort (103 sepsis cases vs 412 non-sepsis controls) was constructed. A predictive model integrating clinical manifestations and laboratory parameters was developed by first pre-selecting variables via a bootstrap-based penalized regression process, followed by Firth penalized logistic regression. The model underwent internal validation and subgroup analysis, with its performance compared against the National Early Warning Score 2 (NEWS2), Systemic Inflammatory Response Syndrome (SIRS), and Quick Sequential Organ Failure Assessment (qSOFA) scoring systems in terms of discrimination, calibration, clinical utility, and cost-effectiveness. Results: The final model incorporated five predictors: temperature dysregulation, nausea or vomiting, fatigue, albumin, and procalcitonin. It demonstrated excellent predictive performance, with a corrected AUC of 0.915 and a calibration slope of 1.022. Subgroup analyses confirmed consistent performance across all subgroups, and the model significantly outperformed NEWS2, SIRS, and qSOFA in predictive accuracy, clinical applicability, and cost-effectiveness. Conclusion: The host-clinical integrated model developed in this study could provide a novel tool for early sepsis risk warning in diabetic patients with acute infections. This approach of integrating host characteristics with the pathophysiology of sepsis may offer new insights for sepsis risk early warning in specific populations. However, external validation in independent cohorts is needed before clinical implementation.

Indexed as

acute infectiondiabeteshost responserisk predictionsepsis

Identifiers

PMID42572776
PMCPMC13453381

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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.