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Blood Pressure Variability and Cerebral Small Vessel Disease: A Systematic Review and Meta-Analysis of
Yuan Ma1, Alex Song2, Anand Viswanathan3
1From the Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA (Y.M., D.B., A.H., S.P.).
Insights
Increased blood pressure variability is linked to a higher risk of white matter hyperintensities, a marker of cerebral small vessel disease. Managing blood pressure variability may help prevent stroke and dementia.
Area of Science:
- Neurology
- Cardiovascular Medicine
- Radiology
Background:
- Blood pressure (BP) variability is a potential risk factor for stroke and dementia.
- Its association with cerebral small vessel disease (CSVD) remains unclear.
- CSVD is a significant contributor to stroke and dementia.
Purpose of the Study:
- To systematically review and meta-analyze studies on BP variability and CSVD.
- To investigate the link between BP variability and markers like white matter hyperintensities, lacunes, and microbleeds.
Main Methods:
- Systematic review and meta-analysis of prospective cohort studies.
- Searched MEDLINE, EMBASE, and Web of Science databases.
- Included 10 studies for qualitative synthesis and 7 for meta-analysis using random-effect models.
Main Results:
- Analyzed data from 2796 individuals (mean age 74 years).
- A one SD increase in systolic BP variability correlated with increased odds of white matter hyperintensities (OR, 1.26).
- No significant association found between systolic BP variability and lacunes or microbleeds.
Conclusions:
- Elevated BP variability may increase the risk of white matter hyperintensities.
- Reducing BP variability could potentially prevent CSVD, stroke, and dementia.
- Future research should address reverse causation and CSVD marker assessment heterogeneity.
Abstract:
Background and Purpose- Blood pressure (BP) variability may increase the risk of stroke and dementia. It remains inconclusive whether BP variability is associated with cerebral small vessel disease, a common and potentially devastating subclinical disease that contributes significantly to both stroke and dementia. Methods- A systematic review and meta-analysis of prospective cohort studies that examined the association between BP variability and the presence or progression of established markers of cerebral small vessel disease, including white matter hyperintensities, lacunes, and microbleeds on magnetic resonance imaging. We searched MEDLINE, EMBASE, and Web of Science. Ten studies met the criteria for qualitative synthesis and 7 could be included in the meta-analysis. Data were synthetized using random-effect models. Results- These studies included a total of 2796 individuals aged 74 (mean) ±4 (SD) years, with a median follow-up of 4.0 years. A one SD increase in systolic BP variability was associated with increased odds of the presence or progression of white matter hyperintensities (odds ratio, 1.26 [95% CI, 1.06-1.50]). The association of systolic BP variability with the presence of lacunes (odds ratio, 0.93 [95% CI, 0.74-1.16]) and the presence of microbleeds (odds ratio, 1.13 [95% CI, 0.89-1.44]) were not statistically significant. Conclusions- A larger BP variability may be associated with a higher risk of having a higher burden of white matter hyperintensities. Targeting large BP variability has the potential to prevent cerebral small vessel disease and thereby reducing the risk of stroke and dementia. The potential issue of reverse causation and the heterogeneity in the assessment of cerebral small vessel disease markers should be better addressed in future studies.
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