Cardiovascular Risk Trajectories and Risk of Developing Stroke and Dementia

痴呆 医学 冲程(发动机) 中风风险 血管性痴呆 情感(语言学) 基线(sea) 风险因素 血管疾病 风险评估 疾病 阿尔茨海默病 终身风险 纵向研究 物理医学与康复 流行病学 中枢神经系统疾病 物理疗法 心脏病学 缺血性中风 心血管健康 梅德林 急诊医学 绝对风险降低 内科学 纵向数据
作者
Pei‐Chun Chen,Ta‐Chen Su,Yun-Yu Chen,Yuan-Teh Lee,Kuo‐Liong Chien
出处
期刊:Neurology [Lippincott Williams & Wilkins]
卷期号:105 (8): e214179-e214179 被引量:1
标识
DOI:10.1212/wnl.0000000000214179
摘要

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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