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Author Spotlight: Assessing the Cardiovascular Profile of Patients with Metabolic Syndrome
Published on: September 27, 2024
A retrospective cohort study on the interaction between arterial stiffness and insulin resistance in chronic heart
Lingyu Ma1, Wei Guo1, Jinhua Bi1
1Department of Cardiology, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, China.
Insights
In chronic heart failure (CHF), high arterial stiffness (ePWV) and insulin resistance (TyG index) significantly increase cardiovascular death risk. Their combined elevation poses a synergistic threat, highlighting the need for integrated management strategies.
Area of Science:
- Cardiology
- Metabolic Syndrome
- Vascular Biology
Background:
- Arterial stiffness and insulin resistance are independent risk factors for chronic heart failure (CHF).
- The interactive relationship between arterial stiffness and insulin resistance in the context of CHF is not well understood.
- Investigating this interaction is crucial for understanding CHF progression and mortality.
Purpose of the Study:
- To investigate the combined impact of arterial stiffness and insulin resistance on cardiovascular mortality in CHF patients.
- To explore the synergistic or additive effects of elevated estimated pulse wave velocity (ePWV) and triglyceride-glucose index (TyG).
- To quantify the interaction effect on cardiovascular mortality risk.
Main Methods:
- Analysis of 1,162 hospitalized CHF patients.
- Calculation of estimated pulse wave velocity (ePWV) and triglyceride-glucose index (TyG).
- Stratification into four groups based on ePWV and TyG medians, employing restricted cubic spline and Cox regression analyses to assess mortality risk and interactions.
Main Results:
- A J-shaped association was observed between ePWV and cardiovascular mortality risk.
- Concomitant elevation of both ePWV and TyG significantly increased cardiovascular mortality risk (HR=2.99).
- Additive interaction analysis revealed a synergistic effect, with 52% of the risk attributable to the interaction between ePWV and TyG.
Conclusions:
- Combined elevation of arterial stiffness (ePWV) and insulin resistance (TyG) significantly elevates cardiovascular mortality risk in CHF patients.
- A synergistic interaction exists between ePWV and TyG, contributing substantially to mortality risk.
- These findings underscore the importance of assessing and managing both arterial stiffness and insulin resistance in CHF management.
Background:
Arterial stiffness and insulin resistance are established risk factors for chronic heart failure (CHF), yet their interaction in CHF remains unclear.
Methods:
We analyzed 1,162 hospitalized CHF patients at Nanjing Drum Tower Hospital. Estimated pulse wave velocity (ePWV) was calculated using a nonlinear function of age and mean blood pressure, and the triglyceride-glucose index (TyG) was calculated based on fasting triglyceride and plasma glucose levels. Participants were stratified into four groups by the medians of ePWV and TyG. Restricted cubic spline (RCS) analysis examined nonlinear associations, while Cox proportional hazards regression assessed cardiovascular mortality risk; additive and multiplicative interactions between ePWV and TyG were further evaluated.
Results:
During a median follow-up of 921 days, 121 cardiovascular deaths occurred. RCS revealed a nonlinear J-shaped association between ePWV and cardiovascular mortality risk (inflection point: 11.36 m/s; 95% CI 11.35-11.38, P for nonlinearity = 0.013). In the combined analysis comparing with the dual-low group, cardiovascular mortality risk was significantly elevated when both markers were above the median (HR = 2.99, 95% CI 1.73-5.17). Controlling for one of the two factors below the median, the isolated elevation of the other marker did not lead to a significant increase in risk. Additive interaction analysis indicated a synergistic effect (RERI = 1.52, 95% CI 0.28-2.99; AP = 0.52, 95% CI 0.08-0.81), whereas multiplicative interaction was nonsignificant (P = 0.065). Findings were consistent across subgroups and robust to sensitivity analyses.
Conclusion:
In CHF, concomitant elevation of ePWV and TyG conferred a 2.99-fold increased risk, with 52% attributable to their interaction.
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