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Multimodal MRI ‐based imputation of the A β + in early mild cognitive impairment
Author(s) -
Tosun Duygu,
Joshi Sarang,
Weiner Michael W.
Publication year - 2014
Publication title -
annals of clinical and translational neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.824
H-Index - 42
ISSN - 2328-9503
DOI - 10.1002/acn3.40
Subject(s) - medicine , magnetic resonance imaging , neuroimaging , positron emission tomography , voxel , cerebral blood flow , alzheimer's disease neuroimaging initiative , pittsburgh compound b , nuclear medicine , cognitive impairment , radiology , pathology , disease , psychiatry
Objective The primary goal of this study was to identify brain atrophy from structural MRI (magnetic resonance imaging) and cerebral blood flow ( CBF ) patterns from arterial spin labeling perfusion MRI that are best predictors of the A β ‐burden, measured as composite 18 F‐AV45‐ PET (positron emission tomography) uptake, in individuals with early mild cognitive impairment ( MCI ). Furthermore, another objective was to assess the relative importance of imaging modalities in classification of A β +/A β − early MCI . Methods Sixty‐seven Alzheimer's Disease Neuroimaging Initiative ( ADNI )‐ GO /2 participants with early MCI were included. Voxel‐wise anatomical shape variation measures were computed by estimating the initial diffeomorphic mapping momenta from an unbiased control template. CBF measures normalized to average motor cortex CBF were mapped onto the template space. Using partial least squares regression, we identified the structural and CBF signatures of A β after accounting for normal cofounding effects of age, gender, and education. Results 18 F‐AV45‐positive early MCI s could be identified with 83% classification accuracy, 87% positive predictive value, and 84% negative predictive value by multidisciplinary classifiers combining demographics data, ApoE ε4‐genotype, and a multimodal MRI ‐based A β score. Interpretation Multimodal MRI can be used to predict the amyloid status of early‐ MCI individuals. MRI is a very attractive candidate for the identification of inexpensive and noninvasive surrogate biomarkers of A β deposition. Our approach is expected to have value for the identification of individuals likely to be A β + in circumstances where cost or logistical problems prevent A β detection using cerebrospinal fluid analysis or A β ‐ PET . This can also be used in clinical settings and clinical trials, aiding subject recruitment and evaluation of treatment efficacy. Imputation of the A β ‐positivity status could also complement A β ‐ PET by identifying individuals who would benefit the most from this assessment.

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