Baseline and longitudinal patterns of brain atrophy in MCI patients, and their use in prediction of short-term conversion to AD: Results from ADNI

被引:433
作者
Misra, Chandan [1 ]
Fan, Yong [1 ]
Davatzikos, Christos [1 ]
机构
[1] Univ Penn, Sch Med, Dept Radiol, Sect Biomed Image Anal, Philadelphia, PA 19104 USA
关键词
Alzheimer's disease; AD; Early detection; Mild cognitive impairment; MCI; Pattern classification; Structural MRI; Imaging biomarker; MILD COGNITIVE IMPAIRMENT; AMYLOID PRECURSOR PROTEIN; PROGRESSIVE PARENCHYMAL DEPOSITION; PRODROMAL ALZHEIMERS-DISEASE; VOXEL-BASED MORPHOMETRY; GRAY-MATTER LOSS; WHITE-MATTER; CEREBRAL INFARCTIONS; HIPPOCAMPAL VOLUME; TEMPORAL-LOBE;
D O I
10.1016/j.neuroimage.2008.10.031
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
High-dimensional pattern classification was applied to baseline and multiple follow-up MRI scans of the Alzheimer's Disease Neuroimaging Initiative (ADNI) participants with mild cognitive impairment (MCI), in order to investigate the potential of predicting short-term conversion to Alzheimer's Disease (AD) on an individual basis. MCI participants that converted to AD (average follow-up 15 months) displayed significantly lower volumes in a number of grey matter (GM) regions, as well as in the white matter (WM). They also displayed more pronounced periventricular small-vessel pathology, as well as an increased rate of increase of such pathology. Individual person analysis was performed using a pattern classifier previously constructed from AD patients and cognitively normal (CN) individuals to yield an abnormality score that is positive for AD-like brains and negative otherwise. The abnormality scores measured from MCI non-converters (MCI-NC) followed a bimodal distribution, reflecting the heterogeneity of this group, whereas they were positive in almost all MCI converters (MCI-C), indicating extensive patterns of AD-like brain atrophy in almost all MCI-C. Both MCI subgroups had similar MMSE scores at baseline. A more specialized classifier constructed to differentiate converters from non-converters based on their baseline scans provided good classification accuracy reaching 81.5%, evaluated via cross-validation. These pattern classification schemes, which distill spatial patterns of atrophy to a single abnormality score, offer promise as biomarkers of AD and as predictors of subsequent clinical progression, on an individual patient basis. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1415 / 1422
页数:8
相关论文
共 77 条
[1]  
Adeli H, 2005, J ALZHEIMERS DIS, V7, P187
[2]  
[Anonymous], BRAIN
[3]   Cleavage of amyloid precursor protein elicited by chronic cerebral hypoperfusion [J].
Bennett, SAL ;
Pappas, BA ;
Stevens, WD ;
Davidson, CM ;
Fortin, T ;
Chen, J .
NEUROBIOLOGY OF AGING, 2000, 21 (02) :207-214
[4]   Hippocampus volume loss due to chronic heavy drinking [J].
Beresford, Thomas P. ;
Arciniegas, David B. ;
Alfers, Julie ;
Clapp, Lori ;
Martin, Brandon ;
Liu, Yiping Du Dengfeng ;
Shen, Dinggang ;
Davatzikos, Christos .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2006, 30 (11) :1866-1870
[5]   Hypercortisolism in alcohol dependence and its relation to hippocampal volume loss [J].
Beresford, Thomas P. ;
Arciniegas, David B. ;
Alfers, Julie ;
Clapp, Lori ;
Martin, Brandon ;
Beresford, Henry F. ;
Du, Yiping ;
Liu, Dengfeng ;
Shen, Dinggang ;
Davatzikos, Christos ;
Laudenslager, Mark L. .
JOURNAL OF STUDIES ON ALCOHOL, 2006, 67 (06) :861-867
[6]   White matter damage in Alzheimer's disease assessed in vivo using diffusion tensor magnetic resonance imaging [J].
Bozzali, M ;
Falini, A ;
Franceschi, M ;
Cercignani, M ;
Zuffi, M ;
Scotti, G ;
Comi, G ;
Filippi, M .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2002, 72 (06) :742-746
[7]  
Braak H, 1998, J NEURAL TRANSM-SUPP, P97
[8]   Early diagnosis of Alzheimer's disease: contribution of structural neuroimaging [J].
Chetelat, G ;
Baron, JC .
NEUROIMAGE, 2003, 18 (02) :525-541
[9]   Mild cognitive impairment -: Can FDG-PET predict who is to rapidly convert to Alzheimer's disease? [J].
Chételat, G ;
Desgranges, B ;
de la Sayette, V ;
Viader, F ;
Eustache, F ;
Baron, JC .
NEUROLOGY, 2003, 60 (08) :1374-1377
[10]  
Chételat G, 2002, NEUROREPORT, V13, P1939