Key result
Each additional functional or depressive limitation is linked to ~21% higher incident CVD risk.
Why the study?
Is a higher descriptive three-domain limitation count (daily-function, walking-distance mobility, and elevated depressive symptoms) associated with an increased risk of incident cardiovascular disease in adults aged >=50 years without baseline cardiovascular disease?
Cohort (n=31,535)
Yes
Is a higher descriptive three-domain limitation count (daily-function, walking-distance mobility, and elevated depressive symptoms) associated with an increased risk of incident cardiovascular disease in adults aged >=50 years without baseline cardiovascular disease?
Hazard Ratio: 1.214 (95% CI 1.109–1.33)
p-value: p=0.012
Across three national ageing cohorts, a higher count of co-occurring daily-function, walking-distance mobility, and depressive-symptom limitations is associated with an increased risk of incident cardiovascular disease in adults aged 50 and older, though it is partially attenuated by broader socioeconomic and comorbidity factors and is not intended as a clinical prediction tool.
Ageing populations experience functional and psychological limitations, but their accumulated cardiovascular relevance across settings is uncertain. We analysed 31,535 adults aged ≥ 50 years without baseline cardiovascular disease in three cohorts. A descriptive three-domain analytic count (0–3) comprised daily-function, walking-distance mobility and elevated depressive-symptom limitations. Cohort-specific Cox models used a common adjustment set across cohorts; estimates were pooled using random effects. During follow-up, 8,950 participants developed cardiovascular disease. Each additional domain was associated with incident cardiovascular disease; the pooled hazard ratio was 1.214 (95% confidence interval 1.109–1.330; 95% prediction interval 1.043–1.414). Compared with no domains, pooled hazard ratios were 1.250 for one domain and 1.517 for ≥ 2 domains. After expanded adjustment for available socioeconomic, behavioural and multimorbidity-related factors, the pooled hazard ratio attenuated to 1.163 (95% confidence interval 1.064–1.271). Findings were similar in sensitivity analyses using common comparable ADL/IADL items and leave-one-cohort-out analyses. Competing-risk estimates differed in HRS, and findings at ≥ 75 years were heterogeneous. The primary estimate is not independent of broader measured factors; the descriptive count is not intended for causal inference, clinical prediction or decision-making.
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Shou et al. (2026) conducted a cohort in Incident cardiovascular disease (n=31,535). Descriptive three-domain limitation count (per one additional limitation domain in daily function, walking-distance mobility, and elevated depressive symptoms) vs. 0 limitation domains (or per 1-domain lower count) was evaluated on Incident cardiovascular disease (self-reported physician-diagnosed heart disease or stroke) (HR 1.214, 95% CI 1.109-1.330, p=0.012). Each additional limitation domain (daily function, mobility, depressive symptoms) was associated with a higher risk of incident cardiovascular disease (pooled HR 1.214, 95% CI 1.109-1.330; P=0.012).
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