Evidence map›Paper›PMID 42222119›Full record

ArticleFrontiers in cardiovascular medicine2026

Development and validation of the C-reactive protein-triglyceride-glucose index for predicting short- and long-term mortality in critically ill patients with coronary artery disease: a multicenter cohort study.

Jian Yang, Yilin Xia, Weixi Guo, Liqun Wu, Xusheng Wu, Bei Li

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Article in Frontiers in cardiovascular medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers 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

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jian YangDepartment of Biomedical Informatics, School of Life Sciences, Central South University, Changsha, China.
Yilin XiaDepartment of Biomedical Informatics, School of Life Sciences, Central South University, Changsha, China.
Weixi GuoDepartment of Biomedical Informatics, School of Life Sciences, Central South University, Changsha, China.
Liqun WuShenzhen Health Development Research and Data Management Center, Shenzhen, China.
Xusheng Wu *Shenzhen Health Development Research and Data Management Center, Shenzhen, China.
Bei Li *Department of Biomedical Informatics, School of Life Sciences, Central South University, Changsha, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The C-reactive protein-triglyceride glucose index (CTI) has been proposed as a novel biomarker of insulin resistance and inflammation, but its association with mortality in critically ill patients with coronary artery disease (CAD) remains unclear. This study aimed to evaluate the associations between the CTI and both short- and long-term all-cause mortality and to assess the predictive value of this index. Methods: Patients with CAD were identified from the MIMIC-IV database and divided into internal training and testing cohorts, while an external validation cohort was derived from the eICU-CRD and Shenzhen Regional Health Information Platform (SRHIP) database. Based on the optimal CTI cut-off values, patients were grouped into three categories. The primary outcomes were short-term (30-day) and long-term (365-day) all-cause mortality. Associations between the CTI and mortality were examined using Kaplan-Meier curves, restricted cubic spline regression, and Cox proportional hazards models. Subgroup, mediation and sensitivity analyses tested result robustness. The CTI was further compared with other single predictors, and six machine learning (ML) models were built to assess its predictive performance. Finally, the SHapley Additive exPlanations (SHAP) analysis identified feature contributions, and a user-friendly web application was developed. Results: The primary cohort included 1,561 patients, and two external validation cohorts included 242 and 105 patients from the eICU-CRD and SRHIP databases. High CTI values were significantly associated with increased short- and long-term mortality, demonstrating a nonlinear dose-response relationship. The CTI exhibited particularly high predictive value for short-term outcomes. The incorporation of the CTI into ML models notably improved the predictive performance, and this improvement was confirmed in the external validation cohort. Conclusions: The CTI was identified as an independent predictor of short- and long-term mortality in critically ill patients with CAD, with a particularly high predictive value for short-term risk stratification. Integrating the CTI into predictive models significantly increased the prognostic accuracy.

Indexed as

coronary artery diseasec-reactive protein-triglyceride-glucose indexinflammationinsulin resistancemachine learning

Identifiers

PMID42222119
PMCPMC13216771

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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.