# Emergency risk stratification using the TyG index: a multi-center cohort study on nonlinear association with 28-day mortality among critically ill patients transferred from the ED to the ICU

**Authors:** Zhenhua Huang, Jianshe Bu, Ke Yu, Wanjie Gu, Haiyan Yin

PMC · DOI: 10.3389/fmed.2025.1605843 · 2025-07-30

## TL;DR

This study shows that the TyG index, a marker of insulin resistance, can help predict 28-day mortality in critically ill patients transferred from the emergency department to the ICU.

## Contribution

The study reveals a nonlinear relationship between the TyG index and mortality risk, identifying a critical threshold for risk stratification in ED-to-ICU patients.

## Key findings

- The TyG index has a nonlinear association with 28-day mortality, with increased risk up to a threshold of 9.84.
- Mortality risk plateaus above a TyG index of 9.84, indicating a saturation effect.
- The association remains robust after adjusting for confounders and across sensitivity analyses.

## Abstract

In the emergency department (ED), rapid risk stratification of critically ill patients is essential for timely intervention. The triglyceride-glucose (TyG) index, a simple marker of insulin resistance, may aid in early mortality prediction, but its utility in ED-to-ICU patients remains unexplored.

Using data from the eICU Collaborative Research Database, we conducted a retrospective multicenter cohort study of 11,593 ED-to-ICU critically ill patients. The TyG index was calculated at ED presentation. The primary outcome was 28-day all-cause mortality. Multivariable Cox regression, restricted cubic splines, and sensitivity analyses were performed to assess associations.

Among patients (mean age 63.6 ± 15.7 years, 57.3% male), 28-day mortality was 6.96%. The relationship between the TyG index and mortality was nonlinear, featuring a critical threshold at a TyG index value of 9.84. Below this cutoff, each unit increase in TyG index significantly elevated mortality risk (HR 1.47, 95% CI 1.20–1.69, p < 0.0001), while above it, the risk plateaued (HR 1.04, 95% CI 1.03–1.05, p = 0.097). The association remained robust after adjustment for confounders (adjusted HR 1.19, 95% CI 1.04–1.35, p = 0.0089) and across sensitivity analyses.

The TyG index, readily obtainable at ED presentation, provides emergency clinicians with a practical tool for early mortality risk stratification in critically ill patients. Its nonlinear association with 28-day mortality suggests a saturation effect, enabling rapid identification of high-risk patients who may benefit from intensified monitoring and intervention.

## Full-text entities

- **Diseases:** diabetes mellitus (MESH:D003920), COPD (MESH:D029424), infection (MESH:D007239), organ failure (MESH:D009102), sepsis (MESH:D018805), septic (MESH:D001170), ischemic stroke (MESH:D002544), multiorgan failure (MESH:D051437), chronic kidney disease (MESH:D051436), abnormal lipid metabolism (MESH:D052439), trauma (MESH:D014947), AMICS (MESH:D012770), ED (MESH:D004630), IR (MESH:D007333), acute respiratory failure (MESH:D012131), hemorrhagic stroke (MESH:D000083302), chronic heart failure (MESH:D006333), endothelial dysfunction (MESH:D014652), hyperglycemia (MESH:D006943), metabolic abnormalities (MESH:D008659), CRD (OMIM:120970), shock (MESH:D012769), acute kidney injury (MESH:D058186), cardiovascular diseases (MESH:D002318), polytrauma (MESH:D009104), acute myocardial infarction (MESH:D009203), cardiac arrest (MESH:D006323), stroke (MESH:D020521), Glasgow coma (MESH:D003128), critical illness (MESH:D016638), DM (MESH:D009223), coronary artery disease (MESH:D003324), inflammation (MESH:D007249), death (MESH:D003643), atherosclerosis (MESH:D050197), infectious (MESH:D003141), metabolic dysregulation (MESH:D021081)
- **Chemicals:** creatinine (MESH:D003404), lipid (MESH:D008055), cholesterol (MESH:D002784), BNU (-), TG (MESH:D014280), nitrogen (MESH:D009584), TC (MESH:D013667), urea (MESH:D014508), glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12343646/full.md

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Source: https://tomesphere.com/paper/PMC12343646