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Cardiovascular Risk Trajectories and Risk of Developing Stroke and Dementia: A Community-Based Cohort Study in Taiwan
Pei-Chun Chen1,2, Ta-Chen Su3,4,5, Yun-Yu Chen6,7
1National Center for Geriatrics and Welfare Research, National Health Research Institutes, Yunlin, Taiwan.
Insights
Accelerated increase in cardiovascular disease (CVD) risk over time significantly elevates the risk of stroke and vascular dementia. Monitoring long-term CVD risk trajectories is crucial for predicting neurological outcomes.
Area of Science:
- Neurology
- Cardiology
- Epidemiology
Background:
- Stroke and dementia share cardiovascular risk factors.
- Longitudinal changes in cardiovascular disease (CVD) risk may better reflect cumulative vascular burden than static scores.
Purpose of the Study:
- To investigate the association between longitudinal CVD risk trajectories and the risk of developing stroke and dementia.
Main Methods:
- Prospective cohort study of 2,335 Taiwanese adults (≥35 years) without prior stroke or dementia.
- Assessed CVD risk using Framingham function at baseline and 3 follow-ups (1990-2000).
- Modeled CVD risk trajectories and linked to national health data for incident stroke/dementia ascertainment.
Main Results:
- Over 21 years, an accelerated CVD risk trajectory (29.2% of participants) was linked to increased risk of all stroke types and vascular dementia.
- Compared to stable CVD risk, accelerated increase showed HRs of 1.81 for all stroke and 2.07 for vascular dementia.
- Higher baseline CVD risk correlated with stroke risk, but less strongly with vascular dementia.
Conclusions:
- Accelerated CVD risk trajectories are associated with elevated risks of stroke and vascular dementia.
- Longitudinal CVD risk patterns may influence vascular dementia risk independently of baseline risk levels.
Background And Objectives:
Stroke and dementia share common cardiovascular risk factors, but few studies have evaluated long-term changes in cardiovascular disease (CVD) risk scores, which may better capture cumulative vascular burden. We aimed to investigate whether the longitudinal trajectory of CVD risk was associated with the risk of developing stroke and dementia.
Methods:
This prospective cohort study included residents aged 35 years and older from a community in northern Taiwan. We included participants without a history of stroke or dementia and assessed CVD risk at baseline (visit 1) and 3 follow-up visits (visits 2-4) from 1990 to 2000 using the Framingham general CVD risk function. CVD risk trajectories were modeled as linear changes over time using a pattern-mixture approach to account for attrition. Incident stroke and dementia were ascertained through linkage to National Health Insurance claims data starting in 2000. In the primary analysis, Cox proportional hazard models were used to estimate adjusted hazard ratios (HRs) for associations of CVD risk trajectory groups with risk of stroke and dementia. In the secondary analysis, we assessed the associations between baseline CVD risk and these outcomes.
Results:
Among 2,335 participants (mean age 52.3 ± 11.2 years; 56.6% women), CVD risk trajectories over 10 years were classified as accelerated increase (29.2%), moderate increase (30.9%), or stable (39.9%). Over a median 21-year follow-up, an accelerated CVD risk trajectory, compared with the stable group, was associated with an increased risk of developing all stroke (HR 1.81, 95% CI 1.40-2.34), ischemic stroke (HR 1.84, 95% CI 1.37-2.48), hemorrhagic stroke (HR 2.38, 95% CI 1.49-3.80), and vascular dementia (HR 2.07, 95% CI 1.03-4.16). The secondary analysis revealed a positive association between baseline CVD risk and risk of developing stroke, but association with vascular dementia was weaker (baseline CVD risk ≥20% vs <10%: for stroke, HR 2.32, 95% CI 1.61-3.33; for vascular dementia, HR 1.84, 95% CI 0.74-4.56). No association was observed with all-cause or nonvascular dementia.
Discussion:
Participants with an accelerated CVD risk had an elevated risk of developing stroke and vascular dementia. Our findings suggested that longitudinal trajectories of CVD risk may affect the risk of vascular dementia beyond individual baseline risks.
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