Neuropathologic features of amnestic mild cognitive impairment

被引:455
作者
Petersen, Ronald C.
Parisi, Joseph E.
Dickson, Dennis W.
Johnson, Kris A.
Knopman, David S.
Boeve, Bradley F.
Jicha, Gregory A.
Ivnik, Robert J.
Smith, Glenn E.
Tangalos, Eric G.
Braak, Heiko
Kokmen, Emre
机构
[1] Mayo Clin & Mayo Fdn, Coll Med, Alzheimers Dis Res Ctr, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Coll Med, Dept Neurol, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Coll Med, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[4] Mayo Clin & Mayo Fdn, Coll Med, Dept Neurosci, Rochester, MN 55905 USA
[5] Mayo Clin & Mayo Fdn, Coll Med, Dept Psychiat & Psychol, Rochester, MN 55905 USA
[6] Mayo Clin & Mayo Fdn, Coll Med, Dept Internal Med, Rochester, MN 55905 USA
[7] Goethe Univ Frankfurt, Inst Clin Anat, D-6000 Frankfurt, Germany
关键词
D O I
10.1001/archneur.63.5.665
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The neuropathologic substrate of amnestic mild cognitive impairment (aMCI) is not known. Objective: To determine the neuropathologic features of patients who died while their clinical classification was aMCI. Design: Cohort study. Setting: Community based. Participants: Sixty-six individuals, including 15 who had memory impairment beyond that allowed for aging but who were not demented, were studied along with 28 clinically healthy individuals and 23 patients with probable Alzheimer disease (AD) for comparison. Main Outcome Measures: Standard neuropathologic techniques and classification according to Khachaturian, Consortium to Establish a Registry for Alzheimer Disease, and National Institute on Aging-Reagan criteria were used to analyze autopsy tissue from 15 individuals who died while their clinical diagnosis was aMCI. For comparison, autopsy data on age-matched groups of clinically healthy individuals and patients with probable AD were analyzed. Results: Most patients with aMCI did not meet the neuropathologic criteria for AD, but their pathologic findings suggest a transitional state of evolving AD. All the patients with aMCI had pathologic findings involving medial temporal lobe structures, likely accounting for their memory impairment. In addition, there were many concomitant pathologic abnormalities, including argyrophilic grain disease, hippocampal sclerosis, and vascular lesions. Conclusions: The neuropathologic features of aMCI matched the clinical features and seemed to be intermediate between the neurofibrillary changes of aging and the pathologic features of very early AD.
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页码:665 / 672
页数:8
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