Visit-To-Visit Blood Pressure Variability and the Risk of Dementia in Older People

被引:40
作者
van Middelaar, Tessa [1 ,2 ]
van Dalen, Jan W. [1 ]
van Gool, Willem A. [1 ]
van den Born, Bert-Jan H. [3 ]
van Vught, Lonneke A. [4 ]
van Charante, Eric P. Moll [4 ]
Richard, Edo [1 ,2 ]
机构
[1] Acad Med Ctr, Dept Neurol, H2-235,Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Donders Inst Brain Cognit & Behav, Dept Neurol, Nijmegen, Netherlands
[3] Acad Med Ctr, Dept Internal Med, Amsterdam, Netherlands
[4] Acad Med Ctr, Amsterdam Publ Hlth Res Inst, Dept Gen Practice, Amsterdam, Netherlands
基金
瑞典研究理事会; 芬兰科学院;
关键词
Blood pressure; blood pressure variability; cognition; cardiovascular disease; dementia; EPISODIC HYPERTENSION; ALZHEIMERS-DISEASE; COGNITIVE FUNCTION; STROKE; PREVENTION; PREDIVA; COHORT; TRIAL;
D O I
10.3233/JAD-170757
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: High visit-to-visit variability (VVV) in blood pressure (BP) is associated with cerebrovascular lesions on neuroimaging. Objective: Our primary objective was to investigate whether VVV is associated with incident all-cause dementia. As a secondary objective, we studied the association of VVV with cognitive decline and cardiovascular disease (CVD). Methods: We included community-dwelling people (age 70-78 year) from the 'Prevention of Dementia by Intensive Vascular Care' (preDIVA) trial with three to five 2-yearly BP measurements during 6-8 years follow-up. VVV was defined using coefficient of variation (CV; SD/meanx100). Cognitive decline was assessed using the Mini-Mental State Examination (MMSE). Incident CVD was defined as myocardial infarction or stroke. We used a Cox proportional hazard regression and mixed-effects model adjusted for sociodemographic factors and cardiovascular risk factors. Results: In 2,305 participants (aged 74.2 +/- 2.5), mean systolic BP over all available visits was 150.1 mmHg (SD 13.6), yielding a CV of 9.0. After 6.4 years (SD 0.8) follow-up, 110 (4.8%) participants developed dementia and 140 (6.1%) CVD. Higher VVV was not associated with increased risk of dementia (hazard ratio [HR] 1.00 per point CV increase; 95% confidence interval [CI] 0.96-1.05), although the highest quartile of VVV was associated with stronger decline in MMSE (beta -0.09, 95% CI -0.17 to -0.01). Higher VVV was associated with incident CVD (HR 1.07; 95% CI 1.04-1.11). Conclusion: In our study among older people, high VVV is not associated with incident all-cause dementia. It is associated with decline in MMSE and incident CVD.
引用
收藏
页码:727 / 735
页数:9
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