Multi-modal imaging predicts memory performance in normal aging and cognitive decline

被引:114
作者
Walhovd, K. B. [1 ,2 ]
Fjell, A. M. [1 ,2 ]
Dale, A. M. [3 ,4 ]
McEvoy, L. K. [4 ]
Brewer, J. [3 ,4 ]
Karow, D. S. [4 ]
Salmon, D. P. [3 ]
Fennema-Notestine, C. [4 ,5 ]
机构
[1] Univ Oslo, Dept Psychol, Ctr Study Human Cognit, N-0317 Oslo, Norway
[2] Ullevaal Univ Hosp, Dept Neuropsychol, Oslo, Norway
[3] Univ Calif San Diego, Dept Neurosci, San Diego, CA 92103 USA
[4] Univ Calif San Diego, Dept Radiol, San Diego, CA 92103 USA
[5] Univ Calif San Diego, Dept Psychiat, San Diego, CA 92103 USA
基金
美国国家卫生研究院;
关键词
MCI; AD; PET; MR morphometry; APOE; Episodic memory; MILD ALZHEIMERS-DISEASE; APOLIPOPROTEIN-E EPSILON-4; POSITRON-EMISSION-TOMOGRAPHY; VOXEL-BASED MORPHOMETRY; SURFACE-BASED ANALYSIS; HUMAN CEREBRAL-CORTEX; EPISODIC MEMORY; HIPPOCAMPAL VOLUME; CORTICAL SURFACE; FDG-PET;
D O I
10.1016/j.neurobiolaging.2008.08.013
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
This study (n = 161) related morphometric MR imaging, EDG-PET and APOE genotype to memory scores in normal controls (NC), mild cognitive impairment (MCI) and Alzheimer's disease (AD). Stepwise regression analyses focused on morphometric and metabolic characteristics of the episodic memory network: hippocampus, entorhinal, parahippocampal, retrosplenial, posterior cingulate, precuneus, inferior parietal, and lateral orbitofrontal cortices. In NC, hippocampal metabolism predicted learning; entorhinal metabolism predicted recognition; and hippocampal metabolism predicted recall. In MCI, thickness of the entorhinal and precuneus cortices predicted learning, while parahippocampal metabolism predicted recognition. In AD, posterior cingulate cortical thickness predicted learning, while APOE genotype predicted recognition. In the total sample, hippocampal volume and metabolism, cortical thickness of the precuneus, and inferior parietal metabolism predicted learning; hippocampal volume and metabolism, parahippocampal thickness and APOE genotype predicted recognition. Imaging methods appear complementary and differentially sensitive to memory in health and disease. Medial temporal and parietal metabolism and morphometry best explained memory variance. Medial temporal characteristics were related to learning, recall and recognition, while parietal structures only predicted learning. (C) 2008 Published by Elsevier Inc.
引用
收藏
页码:1107 / 1121
页数:15
相关论文
共 84 条
[1]  
BARNES J, 2007, NEUROBIOL AGING
[2]   In vivo mapping of gray matter loss with voxel-based morphometry in mild Alzheimer's disease [J].
Baron, JC ;
Chételat, G ;
Desgranges, B ;
Perchey, G ;
Landeau, B ;
de la Sayette, V ;
Eustache, F .
NEUROIMAGE, 2001, 14 (02) :298-309
[3]   [18F]FDG-PET in patients with Alzheimer's disease:: Marker of disease spread [J].
Bittner, D ;
Grön, G ;
Schirrmeister, H ;
Reske, SN ;
Riepe, MW .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2005, 19 (01) :24-30
[4]   Patterns of brain activation in people at risk for Alzheimer's disease [J].
Bookheimer, SY ;
Strojwas, MH ;
Cohen, MS ;
Saunders, AM ;
Pericak-Vance, MA ;
Mazziotta, JC ;
Small, GW .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (07) :450-456
[5]   Self-projection and the brain [J].
Buckner, Randy L. ;
Carroll, Daniel C. .
TRENDS IN COGNITIVE SCIENCES, 2007, 11 (02) :49-57
[6]   Memory and executive function in aging and AD: Multiple factors that cause decline and reserve factors that compensate [J].
Buckner, RL .
NEURON, 2004, 44 (01) :195-208
[7]   Imaging cognition II: An empirical review of 275 PET and fMRI studies [J].
Cabeza, R ;
Nyberg, L .
JOURNAL OF COGNITIVE NEUROSCIENCE, 2000, 12 (01) :1-47
[8]   Functional neuroanatomy of recall and recognition: A PET study of episodic memory [J].
Cabeza, R ;
Kapur, S ;
Craik, FIM ;
McIntosh, AR ;
Houle, S ;
Tulving, E .
JOURNAL OF COGNITIVE NEUROSCIENCE, 1997, 9 (02) :254-265
[9]  
CABEZA R, 2006, CURR OPIN NEUROL, V13, P415
[10]   Neuroimaging and APOE genotype:: A systematic qualitative review [J].
Cherbuin, Nicolas ;
Leach, Liana S. ;
Christensen, Helen ;
Anstey, Kaarin J. .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2007, 24 (05) :348-362