Estimated glucose disposal rate stratifies mortality risk, especially in younger adults with cardiovascular-liver-metabolic overlap.
4 affiliations
- 1Xiyuan Hospital, China Academy of Chinese Medical Sciences, 1 Xiyuan Caochang, Haidian District, Beijing, 100091, China.
- 2Beijing University of Chinese Medicine, Beijing, 100029, China.
- 3Xiyuan Hospital, China Academy of Chinese Medical Sciences, 1 Xiyuan Caochang, Haidian District, Beijing, 100091, China. [email protected].
- 4Xiyuan Hospital, China Academy of Chinese Medical Sciences, 1 Xiyuan Caochang, Haidian District, Beijing, 100091, China. [email protected].
Abstract
Background
The cardiovascular-liver-metabolic (CLM) overlap population faces an elevated risk of mortality, yet prognostic tools integrating dynamic insulin resistance (IR) remain limited. This study aimed to evaluate the prognostic impact of estimated glucose disposal rate (eGDR) on mortality within the CLM overlap population.Methods
An analysis of a prospectively linked national dataset was conducted on 1,126 eligible NHANES participants (1999-2018) with concomitant cardiovascular disease (CVD) and metabolic dysfunction-associated steatotic liver disease (MASLD). eGDR was calculated using clinical parameters. Multivariable Cox regression, restricted cubic splines, Kaplan-Meier survival analysis, and causal mediation models were employed to assess mortality associations and the mediating role of inflammation.Results
Over a median follow-up of 85 months, 453 deaths occurred, including 155 cardiovascular deaths. Lower eGDR showed a borderline inverse association with cardiovascular mortality (HR = 0.84, 95% CI: 0.70-1.01, P = 0.065). eGDR exhibited a threshold-dependent non-linear association with all-cause mortality (P for non-linearity = 0.001), with lower mortality below the inflection point of 5.5901 mg/kg/min (HR = 0.78, 95% CI: 0.66-0.91) and higher mortality above it (HR = 1.16, 95% CI: 0.99-1.36). The pathway from eGDR through systemic inflammation response index (SIRI) to mortality was statistically detectable for all-cause mortality (indirect effect = 6.530, 95% CI: 2.146-11.878), and SIRI mediated 11.3% of the total effect for cardiovascular mortality. Notably, the reduction in mortality risk per 1-unit increase in eGDR was significantly stronger in patients aged < 60 years (all-cause mortality HR = 0.71, 95% CI: 0.60-0.85, P = 0.003; P for interaction = 0.001).Conclusion
In the CLM overlap population, eGDR demonstrates a linear association with cardiovascular mortality and a non-linear association with all-cause mortality, partially mediated by systemic inflammation. Its enhanced prognostic value in younger adults highlights its potential for early risk stratification and could inform targeted interventions focusing on IR-driven pathways.
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BibTeX
@article{zhao2026estimated,
title = {{Estimated glucose disposal rate stratifies mortality risk, especially in younger adults with cardiovascular-liver-metabolic overlap.}},
author = {Mengjie Zhao and Yan Yan and Mengxuan Li and Miaoran Wang and Fang Lu and Qiuyan Li},
journal = {BMC gastroenterology},
year = {2026},
month = jul,
doi = {10.1186/s12876-026-05175-9},
url = {https://europepmc.org/article/MED/42928099},
note = {CC BY-NC-ND},
}
RIS
TY - JOUR
TI - Estimated glucose disposal rate stratifies mortality risk, especially in younger adults with cardiovascular-liver-metabolic overlap.
AU - Mengjie Zhao
AU - Yan Yan
AU - Mengxuan Li
AU - Miaoran Wang
AU - Fang Lu
AU - Qiuyan Li
PY - 2026
DA - 2026/07/28
JO - BMC gastroenterology
DO - 10.1186/s12876-026-05175-9
UR - https://europepmc.org/article/MED/42928099
AB - Background The cardiovascular-liver-metabolic (CLM) overlap population faces an elevated risk of mortality, yet prognostic tools integrating dynamic insulin resistance (IR) remain limited. This study aimed to evaluate the prognostic impact of estimated glucose disposal rate (eGDR) on mortality within the CLM overlap population.Methods An analysis of a prospectively linked national dataset was conducted on 1,126 eligible NHANES participants (1999-2018) with concomitant cardiovascular disease (CVD) and metabolic dysfunction-associated steatotic liver disease (MASLD). eGDR was calculated using clinical parameters. Multivariable Cox regression, restricted cubic splines, Kaplan-Meier survival analysis, and causal mediation models were employed to assess mortality associations and the mediating role of inflammation.Results Over a median follow-up of 85 months, 453 deaths occurred, including 155 cardiovascular deaths. Lower eGDR showed a borderline inverse association with cardiovascular mortality (HR = 0.84, 95% CI: 0.70-1.01, P = 0.065). eGDR exhibited a threshold-dependent non-linear association with all-cause mortality (P for non-linearity = 0.001), with lower mortality below the inflection point of 5.5901 mg/kg/min (HR = 0.78, 95% CI: 0.66-0.91) and higher mortality above it (HR = 1.16, 95% CI: 0.99-1.36). The pathway from eGDR through systemic inflammation response index (SIRI) to mortality was statistically detectable for all-cause mortality (indirect effect = 6.530, 95% CI: 2.146-11.878), and SIRI mediated 11.3% of the total effect for cardiovascular mortality. Notably, the reduction in mortality risk per 1-unit increase in eGDR was significantly stronger in patients aged < 60 years (all-cause mortality HR = 0.71, 95% CI: 0.60-0.85, P = 0.003; P for interaction = 0.001).Conclusion In the CLM overlap population, eGDR demonstrates a linear association with cardiovascular mortality and a non-linear association with all-cause mortality, partially mediated by systemic inflammation. Its enhanced prognostic value in younger adults highlights its potential for early risk stratification and could inform targeted interventions focusing on IR-driven pathways.
SN - 1471-230X
ER -