Key result
Frailty is linked to ~38% higher CVD risk, while a novel proteomic score improves HF discrimination.
Why the study?
The relationship between frailty and CVD requires further validation across diverse populations, and the value of a circulating protein signature for cardiovascular risk assessment remained uncertain.
Does a 20-protein frailty score improve cardiovascular disease and heart failure risk stratification compared to clinical frailty and conventional cardiovascular risk factors in cohort populations?
Cohort (n=88,599)
Yes
Does a 20-protein frailty score improve cardiovascular disease and heart failure risk stratification compared to clinical frailty and conventional cardiovascular risk factors in cohort populations?
A 20-protein plasma frailty signature improves risk discrimination for cardiovascular outcomes, particularly 5-year heart failure risk, beyond clinical frailty and conventional risk factors.
Supports frailty as CVD risk marker in large cohorts; hypothesis-generating and should not yet change practice.
Background Frailty predicts adverse health outcomes, but its relationship with cardiovascular disease (CVD) requires further validation across diverse populations. The value of a circulating protein signature for cardiovascular risk assessment remains uncertain. Methods We examined frailty–CVD associations in the XiDu2017 cohort ( n = 4323) and UK Biobank (UKB; n = 84,276) using logistic and Cox regression, respectively. XiDu longitudinal analyses included 844 participants without baseline CVD. In the UKB proteomic subset, a 20-protein frailty (PF) score was compared with clinical frailty and a model of conventional cardiovascular risk factors. Results Each higher frailty category was associated with prevalent CVD in XiDu (adjusted odds ratio, 1.120; 95% confidence interval [CI], 1.004–1.251). In UKB, frail participants had a higher CVD hazard than robust participants (adjusted hazard ratio, 1.38; 95% CI, 1.28–1.48). For heart failure, the 5-year area under the curve (AUC) was 0.756 for PF and 0.595 for clinical frailty. Adding PF to conventional risk factors increased the optimism-corrected heart failure AUC by 0.113 (95% CI, 0.077–0.142). Conclusions Clinical frailty was associated with cardiovascular outcomes in both cohorts. PF showed incremental discrimination for selected outcomes, particularly heart failure. External validation and evaluation of clinical utility are needed before clinical application.
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Zheng et al. (2026) conducted a cohort in Cardiovascular disease and frailty (n=88,599). Clinical frailty and 20-protein frailty (PF) score vs. Robust participants / conventional cardiovascular risk factors was evaluated on Incident cardiovascular disease (UK Biobank) (HR 1.38, 95% CI 1.28-1.48). Frailty increased CVD risk (adjusted HR 1.38; 95% CI 1.28-1.48), and a 20-protein frailty score improved 5-year heart failure discrimination over clinical frailty (AUC 0.756 vs 0.595).
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