Role of white matter lesions, cerebral atrophy, and APOE on cognition in older persons with and without dementia: The Cache County, Utah, Study of Memory and Aging

被引:31
|
作者
Bigler, ED
Lowry, CM
Kerr, B
Tate, DF
Hessel, CD
Earl, HD
Miller, MJ
Rice, SA
Smith, KH
Tschanz, JT
机构
[1] Brigham Young Univ, Dept Psychol, Provo, UT 84602 USA
[2] Brigham Young Univ, Dept Neurosci, Provo, UT 84602 USA
[3] Univ Utah, Dept Radiol, Salt Lake City, UT 84132 USA
[4] Univ Utah, Dept Psychiat, Salt Lake City, UT 84132 USA
[5] Brigham Young Univ, Dept Psychol, Provo, UT USA
[6] Utah State Univ, Dept Psychol, Logan, UT 84322 USA
[7] Duke Univ, Ctr Med, Dept Psychiat & Behav Sci, Durham, NC 27706 USA
[8] Univ So Calif, Dept Neurol, Los Angeles, CA 90089 USA
关键词
D O I
10.1037/0894-4105.17.3.339
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Neuropsychological, qualitative, and quantitative magnetic resonance imaging findings were examined in subjects with Alzheimer's disease (AD), non-AD dementia or mixed neuropsychiatric disorder, subjects characterized as mild/ambiguous, and controls, all with known apolipoprotein E (APOE) genotype. Neuropsychological tasks included an expanded Consortium to Establish a Registery for Alzheimer's Disease (J. T. Tschanz et al., 2000; K. A. Welsh, J. M. Hoffman, N. L. Earl, & M. W. Hanson 1994) battery and the Mini-Mental Status Examination (M. F. Folstein, S. E. Folstein, & P. R. McHugh, 1975). Periventricular white matter lesions were the most clinically salient, and generalized measures of cerebral atrophy were the most significant quantitative indicators. APOE genotype was unrelated to imaging or neuropsychological performance. Neuropsychological relationships with neuroimaging findings depend on the qualitative or quantitative method used.
引用
收藏
页码:339 / 352
页数:14
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