Morphologic and neuropsychological patterns in patients suffering from Alzheimer's disease

被引:2
作者
Chapuis, Pierre [1 ,2 ]
Sauvee, Mathilde [3 ]
Medici, Maud [4 ]
Serra, Amelie [3 ]
Banciu, Eldda [1 ,2 ]
Moreau-Gaudry, Alexandre [4 ,5 ]
Moreaud, Olivier [3 ]
Krainik, Alexandre [1 ,2 ,6 ]
机构
[1] Univ Hosp Grenoble, Dept Neuroradiol, CS 10217, F-38043 Grenoble 9, France
[2] Univ Hosp Grenoble, MRI, CS 10217, F-38043 Grenoble 9, France
[3] Univ Hosp Grenoble, Dept Neurol, F-38043 Grenoble 9, France
[4] Univ Hosp Grenoble, CIT803, F-38043 Grenoble 9, France
[5] Univ Grenoble 1, Grenoble, France
[6] Grenoble Inst Neurosci, INSERM, U836, Grenoble, France
关键词
Alzheimer dementia; Magnetic resonance imaging; Lobar atrophy of brain; White matter; Neuropsychology; WHITE-MATTER HYPERINTENSITIES; MILD COGNITIVE IMPAIRMENT; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; STRUCTURAL MRI; NORMATIVE DATA; DEMENTIA; CRITERIA; DECLINE;
D O I
10.1007/s00234-016-1659-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction We conducted a retrospective study to identify morphological subgroups of patients referred for AD or aMCI and to seek for differences across neuropsychological performances. Methods One hundred forty-five patients (mean age=76.01, 88 women and 57 men) referred for AD, either at the stage of dementia or aMCI, were examined using structural MRI. Five observers reviewed blindly twice all examinations. We rated microangiopathy, hippocampal, parietal atrophies, including a gradient of fronto-parietal atrophy (GFPA). A multiple component analysis (MCA) followed by a hierarchical ascending classification was conducted to identify morphologically distinct subgroups. Among these, 76 patients completed all the neuropsychological tests. Univariate and multivariate analyses were further conducted on these data across morphological subgroups. The institutional review board approved the research protocol. Results Inter- and intra-raters' agreements were excellent and very good formicroangiopathy and hippocampal atrophy ratings. They were higher for GFPA than for the parietal atrophy scale. MCA without priors identified three groups: group 1 was characterized by no/discrete microangiopathy, severe hippocampal, and predominant parietal atrophy; group 2 had significant microangiopathy, severe hippocampal atrophy, and no predominant parietal atrophy; group 3 had a mild hippocampal atrophy and parietal atrophies. In group 1, working memory profile was less impaired than in group 2 (p = 0.01). Neuropsychological performances of group 3 were higher in most domains. Conclusion Combined characterization of microangiopathy, hippocampal, parietal, and GFPA allows identifying morphological subgroups among patients referred for AD and at risk. These groups have some neuropsychological differences, suggesting different pathophysiological mechanisms or coexisting conditions.
引用
收藏
页码:459 / 466
页数:8
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