Visit-To-Visit Blood Pressure Variability and the Risk of Dementia in Older People
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Published on: June 19, 2019
Tessa van Middelaar1,2, Jan W van Dalen1, Willem A van Gool1
1Department of Neurology, Academic Medical Center (AMC), Amsterdam, The Netherlands.
Insights
High blood pressure variability (VVV) in older adults is not linked to dementia risk but is associated with cognitive decline and cardiovascular disease (CVD). This study highlights VVV as a factor in cognitive function and heart health.
Area of Science:
- Gerontology
- Cardiovascular Medicine
- Neurology
Background:
- High visit-to-visit variability (VVV) in blood pressure (BP) is a known risk factor for cerebrovascular lesions.
- Understanding the impact of BP variability on cognitive health and cardiovascular disease (CVD) is crucial for aging populations.
Purpose of the Study:
- To determine if VVV is associated with incident all-cause dementia in older adults.
- To explore the relationship between VVV and cognitive decline, as well as incident CVD.
Main Methods:
- The study analyzed data from 2,305 community-dwelling older adults (aged 70-78) from the preDIVA trial.
- Blood pressure variability was calculated using the coefficient of variation (CV) from 2-yearly measurements over 6-8 years.
- Cognitive function (MMSE) and incident CVD were assessed, with analyses adjusted for relevant risk factors.
Main Results:
- Higher VVV was not associated with an increased risk of dementia (HR 1.00 per point CV increase).
- The highest quartile of VVV correlated with a greater decline in Mini-Mental State Examination (MMSE) scores (β -0.09).
- Elevated VVV was significantly associated with an increased risk of incident CVD (HR 1.07).
Conclusions:
- In older individuals, high visit-to-visit blood pressure variability does not appear to increase the risk of all-cause dementia.
- However, high VVV is linked to accelerated cognitive decline and a higher incidence of cardiovascular disease.
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/mean×100). 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 (β -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.
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