ASSOCIATION OF MIDLIFE BLOOD-PRESSURE TO LATE-LIFE COGNITIVE DECLINE AND BRAIN MORPHOLOGY

Citation
Ge. Swan et al., ASSOCIATION OF MIDLIFE BLOOD-PRESSURE TO LATE-LIFE COGNITIVE DECLINE AND BRAIN MORPHOLOGY, Neurology, 51(4), 1998, pp. 986-993
Citations number
41
Categorie Soggetti
Clinical Neurology
Journal title
ISSN journal
00283878
Volume
51
Issue
4
Year of publication
1998
Pages
986 - 993
Database
ISI
SICI code
0028-3878(1998)51:4<986:AOMBTL>2.0.ZU;2-E
Abstract
Objective: To investigate the association between midlife systolic blo od pressure (SBP) and late-life cognitive decline and brain morphology in a sample of community-dwelling elderly men 68 to 79 years of age. Methods: Subjects are surviving members from the prospective National Heart, Lung, and Blood Institute Twin Study (intake, 1969 to 1972) who , when examined for a fourth time in 1995 through 1997, underwent brai n MRI and repeated assessment of neurobehavioral functioning. Quantifi cation of the MR images determined cerebral volume and total volume of white matter hyperintensities (WMHIs) for 392 subjects. Midlife SEP l evels measured in 1970, 1980, and 1985 were used to classify subjects into low, medium, and high midlife SEP categories. A 10-year change in performance on the Mini-Mental State Examination, Digit Symbol Substi tution Test, Benton Visual Retention Test, and Verbal Fluency Test was also calculated for these subjects. For all reported analyses, patien ts were treated as genetically unrelated individuals. Results: Subject s with high midlife SEP experienced a greater decline in cognitive per formance and had larger WMHI volumes at follow-up in late life than di d those with low midlife SEP. Decreased brain parenchyma and increased WMHI volumes were associated with decline in neurobehavioral function ing as measured in late life independent of age, education, and baseli ne levels of cognition. Conclusions: Midlife SEP is a significant pred ictor of both decline in cognitive function and MR volumetric measures of brain atrophy in late life. Because decline in neurobehavioral fun ctioning was associated with decreased brain volume and increased WMHI volume, we conclude that the long-term impact of elevated SEP on decl ine in late-life neurobehavioral functioning is Likely to be mediated through its chronic, negative effect on structural characteristics of the brain.