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Predicting Brain Amyloid Positivity from T1 weighted brain MRI and MRI-derived Gray Matter, White Matter and CSF maps using Transfer Learning on 3D CNNs

Abnormal β-amyloid (Aβ) accumulation in the brain is an early indicator of Alzheimer’s disease and practical tests could help identify patients who could respond to treatment, now that promising anti-amyloid drugs are available. Even so, Aβ positivity (Aβ+) is assessed using PET or CSF assays, both...

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Autores principales: Chattopadhyay, Tamoghna, Ozarkar, Saket S., Buwa, Ketaki, Thomopoulos, Sophia I., Thompson, Paul M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949045/
https://www.ncbi.nlm.nih.gov/pubmed/36824826
http://dx.doi.org/10.1101/2023.02.15.528705
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author Chattopadhyay, Tamoghna
Ozarkar, Saket S.
Buwa, Ketaki
Thomopoulos, Sophia I.
Thompson, Paul M.
author_facet Chattopadhyay, Tamoghna
Ozarkar, Saket S.
Buwa, Ketaki
Thomopoulos, Sophia I.
Thompson, Paul M.
author_sort Chattopadhyay, Tamoghna
collection PubMed
description Abnormal β-amyloid (Aβ) accumulation in the brain is an early indicator of Alzheimer’s disease and practical tests could help identify patients who could respond to treatment, now that promising anti-amyloid drugs are available. Even so, Aβ positivity (Aβ+) is assessed using PET or CSF assays, both highly invasive procedures. Here, we investigate how well Aβ+ can be predicted from T1 weighted brain MRI and gray matter, white matter and cerebrospinal fluid segmentations from T1-weighted brain MRI (T1w), a less invasive alternative. We used 3D convolutional neural networks to predict Aβ+ based on 3D brain MRI data, from 762 elderly subjects (mean age: 75.1 yrs. ± 7.6SD; 394F/368M; 459 healthy controls, 67 with MCI and 236 with dementia) scanned as part of the Alzheimer’s Disease Neuroimaging Initiative. We also tested whether the accuracy increases when using transfer learning from the larger UK Biobank dataset. Overall, the 3D CNN predicted Aβ+ with 76% balanced accuracy from T1w scans. The closest performance to this was using white matter maps alone when the model was pre-trained on an age prediction in the UK Biobank. The performance of individual tissue maps was less than the T1w, but transfer learning helped increase the accuracy. Although tests on more diverse data are warranted, deep learned models from standard MRI show initial promise for Aβ+ estimation, before considering more invasive procedures.
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spelling pubmed-99490452023-02-24 Predicting Brain Amyloid Positivity from T1 weighted brain MRI and MRI-derived Gray Matter, White Matter and CSF maps using Transfer Learning on 3D CNNs Chattopadhyay, Tamoghna Ozarkar, Saket S. Buwa, Ketaki Thomopoulos, Sophia I. Thompson, Paul M. bioRxiv Article Abnormal β-amyloid (Aβ) accumulation in the brain is an early indicator of Alzheimer’s disease and practical tests could help identify patients who could respond to treatment, now that promising anti-amyloid drugs are available. Even so, Aβ positivity (Aβ+) is assessed using PET or CSF assays, both highly invasive procedures. Here, we investigate how well Aβ+ can be predicted from T1 weighted brain MRI and gray matter, white matter and cerebrospinal fluid segmentations from T1-weighted brain MRI (T1w), a less invasive alternative. We used 3D convolutional neural networks to predict Aβ+ based on 3D brain MRI data, from 762 elderly subjects (mean age: 75.1 yrs. ± 7.6SD; 394F/368M; 459 healthy controls, 67 with MCI and 236 with dementia) scanned as part of the Alzheimer’s Disease Neuroimaging Initiative. We also tested whether the accuracy increases when using transfer learning from the larger UK Biobank dataset. Overall, the 3D CNN predicted Aβ+ with 76% balanced accuracy from T1w scans. The closest performance to this was using white matter maps alone when the model was pre-trained on an age prediction in the UK Biobank. The performance of individual tissue maps was less than the T1w, but transfer learning helped increase the accuracy. Although tests on more diverse data are warranted, deep learned models from standard MRI show initial promise for Aβ+ estimation, before considering more invasive procedures. Cold Spring Harbor Laboratory 2023-02-16 /pmc/articles/PMC9949045/ /pubmed/36824826 http://dx.doi.org/10.1101/2023.02.15.528705 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Chattopadhyay, Tamoghna
Ozarkar, Saket S.
Buwa, Ketaki
Thomopoulos, Sophia I.
Thompson, Paul M.
Predicting Brain Amyloid Positivity from T1 weighted brain MRI and MRI-derived Gray Matter, White Matter and CSF maps using Transfer Learning on 3D CNNs
title Predicting Brain Amyloid Positivity from T1 weighted brain MRI and MRI-derived Gray Matter, White Matter and CSF maps using Transfer Learning on 3D CNNs
title_full Predicting Brain Amyloid Positivity from T1 weighted brain MRI and MRI-derived Gray Matter, White Matter and CSF maps using Transfer Learning on 3D CNNs
title_fullStr Predicting Brain Amyloid Positivity from T1 weighted brain MRI and MRI-derived Gray Matter, White Matter and CSF maps using Transfer Learning on 3D CNNs
title_full_unstemmed Predicting Brain Amyloid Positivity from T1 weighted brain MRI and MRI-derived Gray Matter, White Matter and CSF maps using Transfer Learning on 3D CNNs
title_short Predicting Brain Amyloid Positivity from T1 weighted brain MRI and MRI-derived Gray Matter, White Matter and CSF maps using Transfer Learning on 3D CNNs
title_sort predicting brain amyloid positivity from t1 weighted brain mri and mri-derived gray matter, white matter and csf maps using transfer learning on 3d cnns
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949045/
https://www.ncbi.nlm.nih.gov/pubmed/36824826
http://dx.doi.org/10.1101/2023.02.15.528705
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