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Blood Pressure Variability and Cerebral Perfusion Decline: A Post Hoc Analysis of the SPRINT MIND Trial
Isabel J Sible1, Daniel A Nation2,3
1Department of Psychology University of Southern California Los Angeles CA.
Insights
Elevated blood pressure variability (BPV) is linked to declining cerebral blood flow (CBF), particularly with standard hypertension treatment. Intensive treatment may mitigate this risk, especially in critical brain regions like the hippocampus.
Area of Science:
- Neurology
- Cardiovascular Medicine
- Medical Imaging
Background:
- Blood pressure variability (BPV) is a known risk factor for cerebrovascular disease and dementia, potentially mediated by cerebral hypoperfusion.
- Observational studies link higher BPV to reduced cerebral blood flow (CBF), but evidence from strictly controlled blood pressure settings is limited.
Purpose of the Study:
- To investigate the relationship between BPV and changes in CBF within the SPRINT MIND trial, comparing intensive versus standard antihypertensive treatment.
- To determine if BPV impacts CBF decline in specific brain regions, including the whole brain, gray matter, white matter, hippocampus, parahippocampal gyrus, and entorhinal cortex.
Main Methods:
- Post hoc analysis of the SPRINT MIND trial involving 289 participants.
- BPV calculated from 4 blood pressure measurements over 9 months post-randomization.
- Cerebral blood flow (CBF) assessed using pseudo-continuous arterial spin labeling MRI at baseline and 4-year follow-up.
Main Results:
- Higher BPV was associated with CBF decline in all measured regions under standard antihypertensive treatment (P=0.03).
- This association was particularly strong in medial temporal regions.
- In the intensive treatment group, elevated BPV was linked to CBF decline only in the hippocampus (P=0.03).
Conclusions:
- Elevated BPV is associated with CBF decline, especially under standard blood pressure-lowering strategies.
- The findings suggest BPV may pose a risk for CBF decline even with tightly controlled mean blood pressure.
- Medial temporal regions showed a robust relationship between BPV and CBF decline, consistent with previous research.
Abstract:
Background Blood pressure variability (BPV) is predictive of cerebrovascular disease and dementia, possibly though cerebral hypoperfusion. Higher BPV is associated with cerebral blood flow (CBF) decline in observational cohorts, but relationships in samples with strictly controlled blood pressure remain understudied. We investigated whether BPV relates to change in CBF in the context of intensive versus standard antihypertensive treatment. Methods and Results In this post hoc analysis of the SPRINT MIND (Systolic Blood Pressure Intervention Trial-Memory and Cognition in Decreased Hypertension) trial, 289 participants (mean, 67.6 [7.6 SD] years, 38.8% women) underwent 4 blood pressure measurements over a 9-month period after treatment randomization (intensive versus standard) and pseudo-continuous arterial spin labeling magnetic resonance imaging at baseline and ≈4-year follow-up. BPV was calculated as tertiles of variability independent of mean. CBF was determined for whole brain, gray matter, white matter, hippocampus, parahippocampal gyrus, and entorhinal cortex. Linear mixed models examined relationships between BPV and change in CBF under intensive versus standard antihypertensive treatment. Higher BPV in the standard treatment group was associated with CBF decline in all regions (ß comparing the first versus third tertiles of BPV in whole brain: -0.09 [95% CI, -0.17 to -0.01]; P=0.03), especially in medial temporal regions. In the intensive treatment group, elevated BPV was related to CBF decline only in the hippocampus (ß, -0.10 [95% CI, -0.18, -0.01]; P=0.03). Conclusions Elevated BPV is associated with CBF decline, especially under standard blood pressure-lowering strategies. Relationships were particularly robust in medial temporal regions, consistent with prior work using observational cohorts. Findings highlight the possibility that BPV remains a risk for CBF decline even in individuals with strictly controlled mean blood pressure levels. Registration URL: http://clinicaltrials.gov. Identifier: NCT01206062.
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