How early can we predict Alzheimer's disease using computational anatomy?

被引:73
作者
Adaszewski, Stanislaw [1 ,2 ]
Dukart, Juergen [1 ]
Kherif, Ferath [1 ]
Frackowiak, Richard [1 ]
Draganski, Bogdan [1 ,3 ]
机构
[1] Univ Lausanne, CHUV, LREN, Dept Neurosci Clin, CH-1011 Lausanne, Switzerland
[2] Warsaw Univ Technol, Dept Neurol, Fac Elect & Informat Technol, Warsaw, Poland
[3] Max Planck Inst Human Cognit & Brain Sci, Leipzig, Germany
基金
瑞士国家科学基金会; 美国国家卫生研究院;
关键词
Structural magnetic resonance imaging; Alzheimer's disease; Mild cognitive impairment; Biomarker; MILD COGNITIVE IMPAIRMENT; PATTERN-CLASSIFICATION; HIPPOCAMPAL ATROPHY; BRAIN ATROPHY; MRI; AD; DIAGNOSIS; CONVERSION; ACCURACY; DEMENTIA;
D O I
10.1016/j.neurobiolaging.2013.06.015
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
Computational anatomy with magnetic resonance imaging (MRI) is well established as a noninvasive biomarker of Alzheimer's disease (AD); however, there is less certainty about its dependency on the staging of AD. We use classical group analyses and automated machine learning classification of standard structural MRI scans to investigate AD diagnostic accuracy from the preclinical phase to clinical dementia. Longitudinal data from the Alzheimer's Disease Neuroimaging Initiative were stratified into 4 groups according to the clinical status-(1) AD patients; (2) mild cognitive impairment (MCI) converters; (3) MCI nonconverters; and (4) healthy controls-and submitted to a support vector machine. The obtained classifier was significantly above the chance level (62%) for detecting AD already 4 years before conversion from MCI. Voxel-based univariate tests confirmed the plausibility of our findings detecting a distributed network of hippocampal-temporoparietal atrophy in AD patients. We also identified a subgroup of control subjects with brain structure and cognitive changes highly similar to those observed in AD. Our results indicate that computational anatomy can detect AD substantially earlier than suggested by current models. The demonstrated differential spatial pattern of atrophy between correctly and incorrectly classified AD patients challenges the assumption of a uniform pathophysiological process underlying clinically identified AD. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:2815 / 2826
页数:12
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