Staging Alzheimer's disease progression with multimodality neuroimaging

被引:66
作者
Ewers, Michael [1 ,2 ]
Frisoni, Giovanni B. [3 ,4 ,5 ]
Teipel, Stefan J. [6 ,7 ]
Grinberg, Lea T. [1 ,8 ]
Amaro, Edson, Jr. [9 ,10 ]
Heinsen, Helmut [11 ]
Thompson, Paul M. [12 ]
Hampel, Harald [13 ]
机构
[1] Univ Calif San Francisco, Dept Radiol, San Francisco, CA 94143 USA
[2] VA Med Ctr, Ctr Imaging Neurodegenerat Dis, San Francisco, CA USA
[3] IRCCS Ctr S Giovanni Dio FBF, LENITEM Lab Epidemiol Neuroimaging & Telemed, Brescia, Italy
[4] AFaR Associaz Fatebenefratelli Ric, Rome, Italy
[5] IRCCS Ctr S Giovanni Dio FBF, Psychogeriatr Ward, Brescia, Italy
[6] Univ Rostock, Dept Psychiat, Rostock, Germany
[7] DZNE, German Ctr Neurodegenerat Disorders, Rostock, Germany
[8] Univ Sao Paulo, Sch Med, Dept Pathol, Sao Paulo, Brazil
[9] Albert Einstein Hosp, Inst Brain, Sao Paulo, Brazil
[10] Univ Sao Paulo, Sch Med, Dept Radiol, Sao Paulo, Brazil
[11] Univ Wurzburg, Dept Psychiat, Morphol Brain Res Unit, D-8700 Wurzburg, Germany
[12] Univ Calif Los Angeles, Sch Med, Dept Neurol, Lab Neuro maging, Los Angeles, CA 90024 USA
[13] Goethe Univ Frankfurt, Dept Psychiat Psychosomat Med & Psychotherapy, Frankfurt, Germany
基金
爱尔兰科学基金会;
关键词
Alzheimer's disease; AD; Mild cognitive impairment; MCI; Pre-dementia; Pre-clinical; Pre-symptomatic; Biological markers; Neuroimaging; Multimodal; Neuropathology; Neuroanatomy; Computational; MRI; fMRI; DTI; VBM; DBM; Tractography; Drug development; Clinical trials; CSF; Staging; Diagnosis classification; Early detection; Prediction; Biological activity; ADNI; EADNI; Regulatory authorities; FDA; MILD COGNITIVE IMPAIRMENT; GRAY-MATTER LOSS; VOXEL-BASED MORPHOMETRY; FIBER TRACT INTEGRITY; MEDIAL TEMPORAL-LOBE; BETA-AMYLOID BURDEN; MINI-MENTAL-STATE; WHITE-MATTER; APOLIPOPROTEIN-E; HIPPOCAMPAL ATROPHY;
D O I
10.1016/j.pneurobio.2011.06.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Rapid developments in medical neuroimaging have made it possible to reconstruct the trajectory of Alzheimer's disease (AD) as it spreads through the living brain. The current review focuses on the progressive signature of brain changes throughout the different stages of AD. We integrate recent findings on changes in cortical gray matter volume, white matter fiber tracts, neuropathological alterations, and brain metabolism assessed with molecular positron emission tomography (PET). Neurofibrillary tangles accumulate first in transentorhinal and cholinergic brain areas, and 4-D maps of cortical volume changes show early progressive temporo-parietal cortical thinning. Findings from diffusion tensor imaging (DTI) for assessment fiber tract integrity show cortical disconnection in corresponding brain networks. Importantly, the developmental trajectory of brain changes is not uniform and may be modulated by several factors such as onset of disease mechanisms, risk-associated and protective genes, converging comorbidity, and individual brain reserve. There is a general agreement between in vivo brain maps of cortical atrophy and amyloid pathology assessed through PET, reminiscent of post mortem histopathology studies that paved the way in the staging of AD. The association between in vivo and post mortem findings will clarify the temporal dynamics of pathophysiological alterations in the development of preclinical AD. This will be important in designing effective treatments that target specific underlying disease AD mechanisms. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:535 / 546
页数:12
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