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Multimodal MRI-based imputation of the Aβ+ in early mild cognitive impairment

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 Aβ-burden, measured as composite (18)F-AV45-PET (positron emission...

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Autores principales: Tosun, Duygu, Joshi, Sarang, Weiner, Michael W, for the Alzheimer's Disease Neuroimaging Initiative
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981105/
https://www.ncbi.nlm.nih.gov/pubmed/24729983
http://dx.doi.org/10.1002/acn3.40
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author Tosun, Duygu
Joshi, Sarang
Weiner, Michael W
for the Alzheimer's Disease Neuroimaging Initiative,
author_facet Tosun, Duygu
Joshi, Sarang
Weiner, Michael W
for the Alzheimer's Disease Neuroimaging Initiative,
author_sort Tosun, Duygu
collection PubMed
description 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 Aβ-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 Aβ+/Aβ− 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 Aβ after accounting for normal cofounding effects of age, gender, and education. RESULTS: (18)F-AV45-positive early MCIs 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 Aβ 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 Aβ deposition. Our approach is expected to have value for the identification of individuals likely to be Aβ+ in circumstances where cost or logistical problems prevent Aβ detection using cerebrospinal fluid analysis or Aβ-PET. This can also be used in clinical settings and clinical trials, aiding subject recruitment and evaluation of treatment efficacy. Imputation of the Aβ-positivity status could also complement Aβ-PET by identifying individuals who would benefit the most from this assessment.
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spelling pubmed-39811052014-10-29 Multimodal MRI-based imputation of the Aβ+ in early mild cognitive impairment Tosun, Duygu Joshi, Sarang Weiner, Michael W for the Alzheimer's Disease Neuroimaging Initiative, Ann Clin Transl Neurol Research Papers 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 Aβ-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 Aβ+/Aβ− 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 Aβ after accounting for normal cofounding effects of age, gender, and education. RESULTS: (18)F-AV45-positive early MCIs 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 Aβ 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 Aβ deposition. Our approach is expected to have value for the identification of individuals likely to be Aβ+ in circumstances where cost or logistical problems prevent Aβ detection using cerebrospinal fluid analysis or Aβ-PET. This can also be used in clinical settings and clinical trials, aiding subject recruitment and evaluation of treatment efficacy. Imputation of the Aβ-positivity status could also complement Aβ-PET by identifying individuals who would benefit the most from this assessment. BlackWell Publishing Ltd 2014-03 2014-02-20 /pmc/articles/PMC3981105/ /pubmed/24729983 http://dx.doi.org/10.1002/acn3.40 Text en © 2014 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Research Papers
Tosun, Duygu
Joshi, Sarang
Weiner, Michael W
for the Alzheimer's Disease Neuroimaging Initiative,
Multimodal MRI-based imputation of the Aβ+ in early mild cognitive impairment
title Multimodal MRI-based imputation of the Aβ+ in early mild cognitive impairment
title_full Multimodal MRI-based imputation of the Aβ+ in early mild cognitive impairment
title_fullStr Multimodal MRI-based imputation of the Aβ+ in early mild cognitive impairment
title_full_unstemmed Multimodal MRI-based imputation of the Aβ+ in early mild cognitive impairment
title_short Multimodal MRI-based imputation of the Aβ+ in early mild cognitive impairment
title_sort multimodal mri-based imputation of the aβ+ in early mild cognitive impairment
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981105/
https://www.ncbi.nlm.nih.gov/pubmed/24729983
http://dx.doi.org/10.1002/acn3.40
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