Key result
Higher TyG index is linked to ~3.4-fold greater odds of aortic stiffness per SD.
Why the study?
The comparative associations and incremental discrimination of insulin resistance surrogate markers for aortic stiffness in asymptomatic adults remain unclear.
Do insulin resistance surrogate markers (TyG index, TyG-BMI, TG/HDL-C) improve discrimination of aortic stiffness in asymptomatic adults?
Cross-Sectional (n=558)
Yes
Do insulin resistance surrogate markers (TyG index, TyG-BMI, TG/HDL-C) improve discrimination of aortic stiffness in asymptomatic adults?
Odds Ratio: 3.44
p-value: p=0.002
The TyG index is strongly associated with aortic stiffness in asymptomatic adults and improves risk discrimination beyond conventional clinical variables.
Extends TyG–aortic stiffness association to asymptomatic adults; hypothesis-generating and should not yet change practice.
Background Insulin resistance surrogate markers, including the triglyceride-glucose (TyG) index, TyG-BMI, and TG/HDL-C ratio, have been associated with aortic stiffness in high-risk populations. Their comparative associations and incremental discrimination in asymptomatic adults remain unclear. We therefore compared these markers and evaluated a simplified model for cfPWV-defined aortic stiffness. Methods We conducted a cross-sectional study of 654 asymptomatic adults aged ≥18 years who underwent routine health examinations at two tertiary medical centers. After exclusions, 457 participants formed the modeling cohort and 101 formed the external validation cohort. Aortic stiffness was defined as cfPWV ≥10 m/s. We used multivariable logistic regression to estimate associations between the three surrogate markers and aortic stiffness. Restricted cubic spline regression assessed potential nonlinear associations. Incremental discrimination was evaluated using Δ AUC, NRI, and IDI. Six machine-learning models were compared, and the most interpretable model was evaluated in an independent institutional validation cohort. Results Aortic stiffness was present in 32.8% (150/457) of the modeling cohort. After full adjustment, the TyG index was independently associated with aortic stiffness (per-SD OR = 3.44, P = 0.002), as were TG/HDL-C (OR = 3.11, P = 0.039) and, more weakly, TyG-BMI (OR = 1.52, P = 0.043). The model including TyG showed higher discrimination ( Δ AUC = 0.014, DeLong P = 0.025) and reclassification (continuous NRI = 0.692 and IDI = 0.041; both P < 0.001) than the base model. A data-derived TyG cutoff of 8.68 was identified as a potential marker for exploratory risk stratification. The five-variable model, comprising age, MAP, diabetes mellitus, smoking, and TyG, yielded AUCs of 0.931 in the modeling cohort and 0.909 in the external validation cohort. Subgroup and sensitivity analyses showed similar patterns. Conclusion Among the three surrogate markers, the TyG index showed the strongest adjusted association with aortic stiffness and the greatest incremental discrimination beyond conventional clinical variables. The five-variable model showed good discrimination in an independent institutional validation cohort. However, these cross-sectional findings support only potential risk-stratification value and do not establish temporal sequence, causality, or clinical utility; prospective studies are required to assess broader generalizability.
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Zhou et al. (2026) conducted a cross-sectional in Aortic stiffness (n=558). Triglyceride-glucose (TyG) index was evaluated on Aortic stiffness (cfPWV ≥10 m/s) (OR 3.44, p=0.002). The TyG index was independently associated with aortic stiffness (per-SD OR 3.44, P=0.002) and provided the greatest incremental discrimination beyond conventional clinical variables in asymptomatic adults.
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