Why the study?
Vascular age can improve cardiovascular risk prediction, but it was unclear whether vascular age calculated by baPWV or cfPWV has a stronger association with cardiovascular events.
Does vascular age calculated by brachial-ankle pulse wave velocity improve cardiovascular risk prediction compared to carotid-femoral pulse wave velocity in a community-based cohort?
Does vascular age calculated by brachial-ankle pulse wave velocity improve cardiovascular risk prediction compared to carotid-femoral pulse wave velocity in a community-based cohort?
Vascular age calculated by brachial-ankle pulse wave velocity is a simple and convenient method that provides better cardiovascular disease risk prediction than carotid-femoral pulse wave velocity in a large Chinese population.
baPWV-derived vascular age may aid CV risk stratification in community cohorts; leaves open whether it outperforms standard models or generalizes beyond this population.
Vascular age (VA) as a surrogate of chronological age can improve cardiovascular risk prediction. This study examines which vascular age calculated by brachial-ankle pulse wave velocity (baPWV) or carotid-femoral pulse wave velocity (cfPWV) has a stronger association with the risk of cardiovascular events. This prospective study included 5723 participants from a community-based atherosclerosis cohort in Beijing, China. VA was defined as the predicted age in a multivariable regression model, including classical cardiovascular risk factors, treatment, and pulse wave velocity (baPWV or cfPWV). Residuals by regressing vascular age on chronological age were defined as ∆-age, and the 10th and 90th percentiles of ∆-age were used as cutoffs to define supernormal vascular aging, normal vascular aging, and early vascular aging, respectively. During the median 3.1-year follow-up period, 173 (3.0%) composite endpoints were observed. After adjusting for age and sex, ∆-age calculated by baPWV was significantly associated with cardiovascular risk (hazard ratio [HR]: 1.05, 95% confidence interval [CI]: 1.01-1.09, p = 0.025). After adjusting for traditional cardiovascular risk factors, early vascular aging group calculated by baPWV had an increased cardiovascular risk (HR: 1.84, 95% CI: 1.25-2.73, p = 0.002), compared with the normal vascular aging group. In contrast, no significant results were observed in the analyses of VA calculated by cfPWV. Since baPWV is a simple and convenient method, VA calculated by baPWV is more valuable for cardiovascular disease risk prediction of large sample population. The association between VA based on baPWV or cfPWV and MACE. EVA early vascular aging, normal VA normal vascular aging, SUPERNOVA supernormal vascular aging.
No takes yet. Share an insight, caveat, or question.
Dong et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: