Blood Pressure Variability and Progression of Clinical Alzheimer Disease

被引:73
作者
de Heus, Rianne A. A. [1 ]
Rikkert, Marcel G. M. Olde [1 ]
Tully, Phillip J. [2 ]
Lawlor, Brian A. [3 ,4 ]
Claassen, Jurgen A. H. R. [1 ]
机构
[1] Radboud Umc Univ, Med Ctr, Dept Geriatr Med, Radboudumc Alzheimer Ctr,Donders Inst Brain Cogni, Nijmegen, Netherlands
[2] Univ Adelaide, Sch Med, Adelaide, SA, Australia
[3] St James Hosp, Mercers Inst Res Ageing, Dublin, Ireland
[4] Trinity Coll Dublin, Dept Med Gerontol, Inst Neurosci, Dublin, Ireland
关键词
activities of daily living; Alzheimer disease; blood pressure; cognition; hypertension; VASCULAR RISK-FACTORS; TO-VISIT VARIABILITY; COGNITIVE DECLINE; ARTERIAL STIFFNESS; FUNCTIONAL DECLINE; EUROPEAN-SOCIETY; DEMENTIA; HYPERTENSION; HEART; HOME;
D O I
10.1161/HYPERTENSIONAHA.119.13664
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Blood pressure variability (BPV) has been shown to have predictive value over blood pressure (BP) levels alone in stroke patients. We assessed whether BPV predicts cognitive and functional decline in Alzheimer disease, using data from a randomized trial (NILVAD [A European Multicentre Double-blind Placebo-controlled Phase III Trial of Nilvadipine in Mild to Moderate Alzheimer's Disease]). Patients with mild-to-moderate Alzheimer disease were included if they had >= 3 office BP measurements available to determine visit-to-visit BPV. Day-to-day BPV was assessed using home BP measurements in a subsample. The variation independent of mean was used to calculate BPV. Outcomes were change in Alzheimer's Disease Assessment Scale-cognitive subscale-12 and Disability Assessment for Dementia after 1 and 1.5 years. A total of 460 patients aged 72.1 (SD=8.1) years, with mean BP of 134.0/75.1 (10.9/6.3) mmHg were included. After 1 year, patients in the highest quartile of BPV had deteriorated more on Alzheimer's Disease Assessment Scale-cognitive subscale compared with patients in the lowest quartile (systolic: beta, 2.24 [95% CI, 0.11-4.38], P=0.040; diastolic: beta, 2.54 [95% CI, 0.33-4.75] P=0.024). This association was still present after 1.5 years (systolic: beta, 2.86 [95% CI, 0.35-5.36], P=0.026; diastolic: beta, 3.30 [95% CI, 0.67-5.93], P=0.014). There was no effect of visit-to-visit BPV on Disability Assessment for Dementia. Day-to-day BPV was available for 46 patients. Significant associations were observed between day-to-day BPV and deterioration on Alzheimer's Disease Assessment Scale-cognitive subscale (systolic: P=0.036) and Disability Assessment for Dementia (systolic: P=0.020; diastolic: P=0.007) after 1 year, but not after 1.5 years. All associations were adjusted for potential confounders, including intervention group. In conclusion, this post hoc analysis indicates that higher visit-to-visit and day-to-day BPV might be associated with progression of Alzheimer disease. Targeting BPV may be a future target to slow decline in patients with Alzheimer disease. Clinical Trial Registration URL: https://www.clinicaltrials.gov. Unique identifier: NCT02017340.
引用
收藏
页码:1172 / 1180
页数:9
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