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Cited by 253

The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.

Midlife Blood Pressure and the Risk of Hippocampal Atrophy: The Honolulu Asia Aging Study

Open access
Korf, Esther S.C., White, Lon R., Scheltens, Philip, Launer, Lenore J.·2004·Hypertension

Abstract

Hippocampal atrophy (HA) is usually attributed to the neurofibrillary tangles and neuritic plaques of Alzheimer disease. However, the hippocampus is vulnerable to global ischemia, which may lead to atrophy. We investigated the association of midlife blood pressure (BP) and late-life HA in a sample of Japanese-American men born between 1900 and 1919. BP was measured on 3 occasions between 1965 and 1971. In 1994 to 1996 a subsample underwent magnetic resonance imaging (MRI) of the brain. Hippocampal volume was estimated by manually drawing regions of interest on relevant scan slices; HA was defined as the lowest quartile of hippocampal volume. Also assessed on the MRI were cortical and subcortical infarcts, lacunes, and white matter hyperintensities. The risk (OR, 95% CI) was estimated for HA associated with systolic (<140 versus ≥140 mm Hg) and diastolic (<90 versus ≥90 mm Hg) BP and with antihypertensive treatment. Analyses were adjusted for sociodemographic factors, other cardiovascular risk factors, apolipoprotein E allele, and correlated brain pathology. Those never treated with antihypertensive medication had a significantly increased risk for HA (OR 1.7; CI=1.12; 2.65). The nontreated subjects with high systolic BP had an increased risk (OR=1.98; CI=0.89; 4.39) for HA. Results were similar for untreated men with high diastolic BP (OR=3.51; CI=1.26; 9.74). In conclusion, treatment with antihypertensive treatment modifies the association of BP and HA, such that high levels of BP adversely affect the hippocampus in persons never treated with antihypertensives.

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Metadata

Authors
Korf, E. S. C., White, L. R., Scheltens, P., & Launer, L. J.
Venue
Hypertension
Published
2004-07
Volume
44
Issue
1
Pages
29-34
ISSN
  • 0194-911X (ISSN-L)
  • 1524-4563
OpenAlex
W2140174213
Cited by
253
References
11
FWCI
6.95
Type
journal article
Language
en
Open access
bronze

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