Brain mechanisms of successful compensation during learning in Alzheimer disease

被引:99
作者
Gould, R. L.
Arroyo, B.
Brown, R. G.
Owen, A. M.
Bullmore, E. T.
Howard, R. J.
机构
[1] Kings Coll London, Old Age Psychiat Sect, Inst Psychiat, MRC Ctr Neurodegenerat Res, London SE5 8AF, England
[2] Kings Coll London, Maudsley Hosp, London WC2R 2LS, England
[3] Kings Coll London, Inst Psychiat, Dept Psychol, London WC2R 2LS, England
[4] MRC Cognit & Brain Sci Unit, Cambridge, England
[5] Univ Cambridge, Dept Psychiat, Cambridge, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1212/01.wnl.0000237534.31734.1b
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To determine whether patients with Alzheimer disease (AD) compensate for neuropathologic changes when performing a mnemonic task by recruiting 1) the same brain regions as age-matched, healthy controls, but to a greater extent; 2) additional brain regions not activated by controls; or 3) both. Methods: Twelve patients with mild probable AD and 12 healthy age-and education-matched controls participated in an fMRI study of successful encoding and retrieval of visuospatial paired associates. To ensure successful performance in both groups, participants were given multiple attempts to learn associations between two and three object locations. Results: The pattern of brain activity in patients with AD performing an easy version of the task was indistinguishable from that of controls performing a harder version of the task. Increased activation in left medial and right lateral prefrontal cortices was found in patients with AD compared to controls during encoding of two object locations, but not when this level of encoding in patients was compared with encoding of three object locations in controls. Conclusions: There was no evidence of neural plasticity in the form of recruitment of novel brain regions in patients with Alzheimer disease. Data supported greater recruitment of the same brain regions as age-matched controls as a means of compensating for neuropathology and associated cognitive impairment in Alzheimer disease.
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收藏
页码:1011 / 1017
页数:7
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