24-Hour Blood Pressure Variability Via Ambulatory Monitoring and Risk for Probable Dementia in the SPRINT Trial - 21/11/24

Doi : 10.14283/jpad.2024.35 
I.J. Sible 1, Daniel A. Nation 2, 3,
1 Department of Psychology, University of Southern California, 90089, Los Angeles, CA, USA 
2 Leonard Davis School of Gerontology, University of Southern California, 3715 McClintock Ave, 90089, Los Angeles, CA, USA 
3 Zilkha Neurogenetic Institute, Department of Physiology and Neuroscience, University of Southern California, 90089, Los Angeles, CA, USA 

b danation@usc.edu danation@usc.edu

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Abstract

Background

Blood pressure variability is an emerging risk factor for dementia, independent and oftentimes beyond mean blood pressure levels. Recent evidence from interventional cohorts with rigorously controlled mean blood pressure levels suggest blood pressure variability over months to years remains a risk for dementia, but no prior studies have investigated relationships with blood pressure variability over shorter time periods.

Objectives

To investigate the potential effect of ambulatory blood pressure variability on the rate of cognitive outcomes under intensive vs standard blood pressure lowering.

Design

Post hoc analysis of the randomized, controlled, open-label Systolic Blood Pressure Intervention Trial clinical trial.

Setting

Multisite Systolic Blood Pressure Intervention Trial.

Participants

793 participants at increased risk for cardiovascular disease and without history of dementia at study randomization.

Intervention

Standard (<140 mmHg systolic blood pressure target) vs intensive (<120 mmHg systolic blood pressure target) lowering of mean blood pressure.

Measurements

24-hour ambulatory blood pressure monitoring 27 months after treatment randomization (standard vs intensive) and follow-up cognitive testing. Intraindividual blood pressure variability was calculated as the average real variability over 24-hour, daytime, and nighttime periods. Participants were categorized into 3 adjudicated clinical outcomes: no cognitive impairment, mild cognitive impairment, probable dementia. Cox proportional hazards models examined the potential effect of ambulatory blood pressure variability on the rate of cognitive outcomes under intensive vs standard blood pressure lowering. Associations with mean blood pressure were also explored.

Results

Higher systolic 24-hour blood pressure variability was associated with increased risk for probable dementia in the standard group (adjusted hazard ratio [HR]: 2.56 [95% CI 1.16, 5.62], p = 0.019) but not in the intensive group (HR: 0.54 [95% CI 0.24, 1.23], p = 0.141). Similar findings were observed with daytime systolic blood pressure variability but not nighttime blood pressure variability. Mean blood pressure was not associated with cognitive outcomes.

Conclusions

Higher systolic 24-hour and daytime blood pressure variability via ambulatory monitoring is associated with risk for dementia under standard blood pressure treatment. Findings support prior evidence that blood pressure variability remains a risk for dementia despite strict control of mean blood pressure levels.

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Key words : Blood pressure variability, dementia, antihypertensives, ambulatory blood pressure monitoring


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 Clinical trial information: ClinicalTrials.gov; NCT01206062.
Disclosures: None.


© 2024  THE AUTHORS. Published by Elsevier Masson SAS on behalf of SERDI Publisher.. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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Vol 11 - N° 3

P. 684-692 - Maggio 2024 Ritorno al numero
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