Evidence mapPaperPMID 40346649Full record

Observational studyCardiovascular diabetology2025

Combined assessment of stress hyperglycemia ratio and glycemic variability to predict all-cause mortality in critically ill patients with atherosclerotic cardiovascular diseases across different glucose metabolic states: an observational cohort study with machine learning.

Fuxu Wang, Yu Guo, Yuru Tang, Shuangmei Zhao, Kaige Xuan, Zhi Mao, Ruogu Lu, Rongyao Hou, Xiaoyan Zhu

Abstract readObservational StudyComparative Study
In one paragraph

Observational study in Cardiovascular diabetology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

9 authors.

Fuxu Wang *Department of Critical Care Medicine, The Affiliated Hospital of Qingdao University, Qingdao, China.
Yu Guo *Department of Neurology, The Affiliated Hospital of Qingdao University, Qingdao, China.
Yuru Tang *Department of Critical Care Medicine, The Affiliated Hospital of Qingdao University, Qingdao, China.
Shuangmei ZhaoDepartment of Critical Care Medicine, The Affiliated Hospital of Qingdao University, Qingdao, China.
Kaige XuanDepartment of Critical Care Medicine, The Affiliated Hospital of Qingdao University, Qingdao, China.
Zhi MaoDepartment of Critical Care Medicine, The First Medical Center of PLA General Hospital, Beijing, China.
Ruogu LuMedical Innovation Research Department, Chinese PLA General Hospital, Beijing, China. ruogulu2023@163.com.
Rongyao HouDepartment of Neurology, The Affiliated Hiser Hospital of Qingdao University, Qingdao, China. hrysdzc@qdu.edu.cn.
Xiaoyan ZhuDepartment of Critical Care Medicine, The Affiliated Hospital of Qingdao University, Qingdao, China. zxysdjm@qdu.edu.cn.

Funding

the National Natural Science Foundation of China 82171299, 82271346
6 · The paper itself

Abstract

backgroundStress hyperglycemia ratio (SHR) and glycemic variability (GV) reflect acute glucose elevation and fluctuations, which correlate with adverse outcomes in patients with atherosclerotic cardiovascular disease (ASCVD). However, the prognostic significance of combined SHR-GV evaluation for ASCVD mortality remains unclear. This study examines associations of SHR, GV, and their synergistic effects with mortality in patients with ASCVD across different glucose metabolic states, incorporating machine learning (ML) to identify critical risk factors influencing mortality.

methodsPatients with ASCVD were screened in the Medical Information Mart for Intensive Care IV (MIMIC-IV) database and stratified into normal glucose regulation (NGR), pre-diabetes mellitus (Pre-DM), and diabetes mellitus (DM) groups based on glucose metabolic status. The primary endpoint was 28-day mortality, with 90-day mortality as the secondary outcome. SHR and GV levels were categorized into tertiles. Associations with mortality were analyzed using Kaplan-Meier(KM) curves, Cox proportional hazards models, restricted cubic splines (RCS), receiver operating characteristic (ROC) curves, landmark analyses, and subgroup analyses. Five ML algorithms were employed for mortality risk prediction, with SHapley Additive exPlanations (SHAP) applied to identify critical predictors.

resultsA total of 2807 patients were included, with a median age of 71 years, and 58.78% were male. Overall, 483 (23.14%) and 608 (29.13%) patients died within 28 and 90 days of ICU admission, respectively. In NGR and Pre-DM subgroups, combined SHR-GV assessment demonstrated superior predictive performance for 28-day mortality versus SHR alone [NGR: AUC 0.688 (0.636-0.739) vs. 0.623 (0.568-0.679), P = 0.028; Pre-DM: 0.712 (0.659-0.764) vs. 0.639 (0.582-0.696), P = 0.102] and GV alone [NGR: 0.688 vs. 0.578 (0.524-0.633), P < 0.001; Pre-DM: 0.712 vs. 0.593 (0.524-0.652), P < 0.001]. Consistent findings were observed for 90-day mortality prediction. However, in the DM subgroup, combined assessment improved prediction only for 90-day mortality vs. SHR alone [AUC 0.578 (0.541-0.616) vs. 0.560 (0.520-0.599), P = 0.027], without significant advantages in other comparisons.

conclusionsCombined SHR and GV assessment serves as a critical prognostic tool for ASCVD mortality, providing enhanced predictive accuracy compared to individual metrics, particularly in NGR and Pre-DM patients. This integrated approach could inform personalized glycemic management strategies, potentially improving clinical outcomes.

Indexed as

AtherosclerosisBlood GlucoseDiabetes MellitusHyperglycemiaMachine LearningPrediabetic StateStress, PhysiologicalAgedBiomarkersCause of DeathCritical IllnessDatabases, FactualFemaleHumansMaleMiddle AgedBiomarkersBlood GlucoseAtherosclerotic cardiovascular diseaseGlycemic variabilityMachine learningMIMIC-IV databaseStress hyperglycemia ratio

Identifiers

PMID40346649
PMCPMC12065353

What Socratic 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 Socratic graph.