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Midlife blood pressure, plasma beta-amyloid, and the risk for Alzheimer disease: the Honolulu Asia Aging Study

TitleMidlife blood pressure, plasma beta-amyloid, and the risk for Alzheimer disease: the Honolulu Asia Aging Study
Publication TypeJournal Article
Year of Publication2012
AuthorsShah, NS, Vidal, JS, Masaki, K, Petrovitch, H, Ross, GW, Tilley, C, DeMattos, RB, Tracy, RP, White, LR, Launer, LJ
JournalHypertensionHypertension
Volume59
Pagination780-6
Date PublishedApr
ISBN Number1524-4563 (Electronic)<br/>0194-911X (Linking)
Accession Number22392902
KeywordsAged, Aged, 80 and Over, Alzheimer Disease/blood/ epidemiology/ physiopathology, Amyloid beta-Peptides/ blood, Autopsy, Biological Markers/blood, Blood Pressure/ physiology, Brain/pathology, Dementia/blood/ epidemiology/ physiopathology, Hawaii, Humans, Hypertension/complications/physiopathology, Longitudinal Studies, Male, Middle Aged, Neurofibrillary Tangles/pathology, Plaque, Amyloid/pathology, Prospective Studies, Retrospective Studies, Risk Factors
Abstractbeta-Amyloid (Abeta), a vasoactive protein, and elevated blood pressure (BP) levels are associated with Alzheimer disease (AD) and possibly vascular dementia. We investigated the joint association of midlife BP and Abeta peptide levels with the risk for late-life AD and vascular dementia. Subjects were 667 Japanese-American men (including 73 with a brain autopsy), from the prospective Honolulu Heart Program/Honolulu Asia Aging Study (1965-2000). Midlife BP was measured starting in 1971 in participants with a mean age of 58 years; Abeta was measured in specimens collected in 1980-1982, and assessment of dementia and autopsy collection started in 1991-1993. The outcome measures were prevalent (present in 1991-1993) and incident AD (n=53, including 38 with no contributing cardiovascular disease) and vascular dementia (n=24). Cerebral amyloid angiopathy, beta-amyloid neuritic plaques, and neurofibrillary tangles were evaluated in postmortem tissue. The risk for AD significantly increased with lower levels of plasma Abeta (Abeta1-40 hazard ratio: 2.1 [95% CI: 1.4 to 3.1]; Abeta1-42 hazard ratio: 1.6 [95% CI: 1.1 to 2.3]). Evidence of interaction between diastolic BP and plasma Abeta (1-40 P(interaction)/=15 years before AD is diagnosed, and the association of Abeta to AD is modulated by midlife diastolic BP. Elevated BP may compromise vascular integrity leading to cerebral amyloid angiopathy and impaired Abeta clearance from the brain.
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