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Published online before print May 11, 2005, doi:10.1212/01.WNL.0000164712.24389.BB)
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Volume 64, Number 11, June 14, 2005
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01.WNL.0000164712.24389.BBv1
64/11/1846    most recent
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NEUROLOGY 2005;64:1846-1852
© 2005 American Academy of Neurology

Ambulatory blood pressure and the brain

A 5-year follow-up

Iris B. Goldstein, PhD, George Bartzokis, MD, Donald Guthrie, PhD and David Shapiro, PhD

From the Departments of Psychiatry and Biobehavioral Sciences and Neurology, University of California, Los Angeles.

Address correspondence and reprint requests to Dr. Iris B. Goldstein, UCLA Department of Psychiatry, 760 Westwood Plaza, Los Angeles, CA 90095-1759; e-mail: irisg{at}ucla.edu

Objective: To determine if initial values of casual and ambulatory systolic blood pressure (SBP) predict white matter hyperintensities, insular subcortex hyperintensities, and brain atrophy 5 years later in a group of healthy elderly individuals.

Methods: The authors studied 155 healthy men and women, aged 55 to 79 years. Two 24-hour ambulatory blood pressure (BP) sessions assessed BP level and variability during waking and sleep. Hyperintensities and total brain volume were quantified by MRI. Procedures were repeated 5 years later in 78% (121) of subjects.

Results: Hyperintensities and brain atrophy increased over time, with greater increases among older subjects. The presence of increased BP level and variability initially and again 5 years later had negative consequences for the brain. Independent of age, the greater the initial SBP, the greater the likelihood that individuals would have severe white matter hyperintensities after 5 years. Also, elevated casual SBP was associated with severe insular subcortex hyperintensities and greater SBP sleep variability with increased brain atrophy.

Conclusions: Among healthy elderly individuals whose initial, average, casual blood pressure (BP) was relatively low (116.9/71.1 mm Hg), small increases in casual and 24-hour ambulatory BP measures were associated with greater brain atrophy and subcortical lesions after 5 years.


Editorial, see page 1832

Supported by Research Grant AG-11595 from the National Institute of Aging.

Received May 28, 2004. Accepted in final form March 15, 2005.




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