Risk factors for cerebral hypoperfusion, mild cognitive impairment, and dementia

被引:162
作者
Meyer, JS
Rauch, G
Rauch, RA
Haque, A
机构
[1] Vet Affairs Med Ctr, Cerebral Blood Flow Lab, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Neurol, Houston, TX 77030 USA
[3] Vet Affairs Med Ctr, Serv Radiol, Houston, TX 77030 USA
关键词
aging; dementia; cognitive decline; risk factors; cerebral hypoperfusion; Xe-CT CBF; neuroimaging;
D O I
10.1016/S0197-4580(00)00136-6
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Putative risk factors accelerating mild cognitive decline and dementia were correlated with repeated measures of cerebral atrophy, CT, densitometry, perfusions, and cognitive testing among neurologically and cognitively normative aging volunteers. A total of 224 normative subjects at increased risk for cognitive decline were admitted to the study. Mean entry age was 59.5 +/- 15.8 years. Mean follow-up is 5.8 +/- 3.3 years. At follow-up, 22 developed mild cognitive impairment (41 CCSE greater than or equal to -3), 19 became demented-8 with Vascular type (VAD), 11 with Alzheimer's type (DAT)-and 183 remain cognitively unchanged. Cerebral atrophy, tissue densities, and perfusions were measured by Xe-CT. After age 60, cerebral atrophy, ventricular enlargement, and polio- and leuko-araiosis geometrically increased as perfusions declined. Risk factors accelerating perfusional decline, cerebral atrophy, polio-araiosis, and leuko-araiosis were: transient ischemic attacks (TIAs), hypertension, smoking, hyperlipidemia, and male gender. At age 71.5 +/- 11.9, mild cognitive impairment began accelerated by TIAs, hypertension and heart disease. Leuko-araiosis began before cognitive decline. TIAs, hypertension, and hyperlipidemia correlated with VAD. Excessive cortical perfusional decrease, gray and white matter hypodensities, and cerebral atrophy correlate with cognitive decline. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:161 / 169
页数:9
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