Cerebrovascular and brain morphologic correlates of mild cognitive impairment in the national heart, lung, and blood institute twin study

Citation
C. Decarli et al., Cerebrovascular and brain morphologic correlates of mild cognitive impairment in the national heart, lung, and blood institute twin study, ARCH NEUROL, 58(4), 2001, pp. 643-647
Citations number
51
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
ARCHIVES OF NEUROLOGY
ISSN journal
00039942 → ACNP
Volume
58
Issue
4
Year of publication
2001
Pages
643 - 647
Database
ISI
SICI code
0003-9942(200104)58:4<643:CABMCO>2.0.ZU;2-Y
Abstract
Objective: To evaluate the relative risk (RR) of mild cognitive impairment (MCI) associated with cerebrovascular risk factors and cerebrovascular-rela ted brain changes. Design: Mild cognitive impairment was determined for the subjects of the pr ospective National Heart, Lung, and Blood Institute Twin Study. Quantitativ e measures of brain, white matter hyperintensity, cerebral infarction, apol ipoprotein E genotype, and psychometric testing were obtained. Results: Subjects with MCI were older (73.5 +/-3.0 vs 72.1 +/-2.8 years), c onsumed less alcohol (3.7 +/-5.8 vs 7.0 +/- 10.7 drinks per week), had grea ter white matter hyperintensity volumes (0.56%+/-0.82% vs 0.25%+/-0.34% of cranial volume), and had an increased prevalence of apolipoprotein E4 genot ype (31.4% vs 19.2%) than normal subjects. White matter hyperintensity and the presence of the apolipoprotein E4 genotype were associated with a signi ficantly increased risk for MCI. When all subjects were included in the ana lysis, alcohol consumption was associated with a reduced risk for MCI (RR=0 .93, P<.05). When subjects with a history of symptomatic cerebrovascular di sease were excluded from the analysis, elevated midlife diastolic blood pre ssure was associated with an increased risk for MCI (RR=1.70, P<.05). Conclusions: Elevated midlife blood pressures, and the resulting increased white matter hyperintensities, increase the risk for MCI in a group of comm unity-dwelling older men to at least the same degree as apolipoprotein E4 g enotype. Given the common occurrence of elevations in midlife blood pressur e, early and effective treatment may be warranted to prevent late-life brai n abnormalities and MCI. Moreover, since many individuals with MCI progress to clinical dementia, longitudinal evaluations of this cohort will be impo rtant.