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A deep neural network estimation of brain age is sensitive to cognitive impairment and decline

The greatest known risk factor for Alzheimer’s disease (AD) is age. While both normal aging and AD pathology involve structural changes in the brain, their trajectories of atrophy are not the same. Recent developments in artificial intelligence have encouraged studies to leverage neuroimaging-derive...

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Autores principales: Yang, Yisu, Sathe, Aditi, Schilling, Kurt, Shashikumar, Niranjana, Moore, Elizabeth, Dumitrescu, Logan, Pechman, Kimberly R., Landman, Bennett A., Gifford, Katherine A., Hohman, Timothy J., Jefferson, Angela L., Archer, Derek B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10461919/
https://www.ncbi.nlm.nih.gov/pubmed/37645837
http://dx.doi.org/10.1101/2023.08.10.552494
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author Yang, Yisu
Sathe, Aditi
Schilling, Kurt
Shashikumar, Niranjana
Moore, Elizabeth
Dumitrescu, Logan
Pechman, Kimberly R.
Landman, Bennett A.
Gifford, Katherine A.
Hohman, Timothy J.
Jefferson, Angela L.
Archer, Derek B.
author_facet Yang, Yisu
Sathe, Aditi
Schilling, Kurt
Shashikumar, Niranjana
Moore, Elizabeth
Dumitrescu, Logan
Pechman, Kimberly R.
Landman, Bennett A.
Gifford, Katherine A.
Hohman, Timothy J.
Jefferson, Angela L.
Archer, Derek B.
author_sort Yang, Yisu
collection PubMed
description The greatest known risk factor for Alzheimer’s disease (AD) is age. While both normal aging and AD pathology involve structural changes in the brain, their trajectories of atrophy are not the same. Recent developments in artificial intelligence have encouraged studies to leverage neuroimaging-derived measures and deep learning approaches to predict brain age, which has shown promise as a sensitive biomarker in diagnosing and monitoring AD. However, prior efforts primarily involved structural magnetic resonance imaging and conventional diffusion MRI (dMRI) metrics without accounting for partial volume effects. To address this issue, we post-processed our dMRI scans with an advanced free-water (FW) correction technique to compute distinct FW-corrected fractional anisotropy (FA(FWcorr)) and FW maps that allow for the separation of tissue from fluid in a scan. We built 3 densely connected neural networks from FW-corrected dMRI, T1-weighted MRI, and combined FW+T1 features, respectively, to predict brain age. We then investigated the relationship of actual age and predicted brain ages with cognition. We found that all models accurately predicted actual age in cognitively unimpaired (CU) controls (FW: r=0.66, p=1.62×10(−32); T1: r=0.61, p=1.45×10(−26), FW+T1: r=0.77, p=6.48×10(−50)) and distinguished between CU and mild cognitive impairment participants (FW: p=0.006; T1: p=0.048; FW+T1: p=0.003), with FW+T1-derived age showing best performance. Additionally, all predicted brain age models were significantly associated with cross-sectional cognition (memory, FW: β=−1.094, p=6.32×10(−7); T1: β=−1.331, p=6.52×10(−7); FW+T1: β=−1.476, p=2.53×10(−10); executive function, FW: β=−1.276, p=1.46×10(−9); T1: β=−1.337, p=2.52×10(−7); FW+T1: β=−1.850, p=3.85×10(−17)) and longitudinal cognition (memory, FW: β=−0.091, p=4.62×10(−11); T1: β=−0.097, p=1.40×10(−8); FW+T1: β=−0.101, p=1.35×10(−11); executive function, FW: β=−0.125, p=1.20×10(−10); T1: β=−0.163, p=4.25×10(−12); FW+T1: β=−0.158, p=1.65×10(−14)). Our findings provide evidence that both T1-weighted MRI and dMRI measures improve brain age prediction and support predicted brain age as a sensitive biomarker of cognition and cognitive decline.
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spelling pubmed-104619192023-08-29 A deep neural network estimation of brain age is sensitive to cognitive impairment and decline Yang, Yisu Sathe, Aditi Schilling, Kurt Shashikumar, Niranjana Moore, Elizabeth Dumitrescu, Logan Pechman, Kimberly R. Landman, Bennett A. Gifford, Katherine A. Hohman, Timothy J. Jefferson, Angela L. Archer, Derek B. bioRxiv Article The greatest known risk factor for Alzheimer’s disease (AD) is age. While both normal aging and AD pathology involve structural changes in the brain, their trajectories of atrophy are not the same. Recent developments in artificial intelligence have encouraged studies to leverage neuroimaging-derived measures and deep learning approaches to predict brain age, which has shown promise as a sensitive biomarker in diagnosing and monitoring AD. However, prior efforts primarily involved structural magnetic resonance imaging and conventional diffusion MRI (dMRI) metrics without accounting for partial volume effects. To address this issue, we post-processed our dMRI scans with an advanced free-water (FW) correction technique to compute distinct FW-corrected fractional anisotropy (FA(FWcorr)) and FW maps that allow for the separation of tissue from fluid in a scan. We built 3 densely connected neural networks from FW-corrected dMRI, T1-weighted MRI, and combined FW+T1 features, respectively, to predict brain age. We then investigated the relationship of actual age and predicted brain ages with cognition. We found that all models accurately predicted actual age in cognitively unimpaired (CU) controls (FW: r=0.66, p=1.62×10(−32); T1: r=0.61, p=1.45×10(−26), FW+T1: r=0.77, p=6.48×10(−50)) and distinguished between CU and mild cognitive impairment participants (FW: p=0.006; T1: p=0.048; FW+T1: p=0.003), with FW+T1-derived age showing best performance. Additionally, all predicted brain age models were significantly associated with cross-sectional cognition (memory, FW: β=−1.094, p=6.32×10(−7); T1: β=−1.331, p=6.52×10(−7); FW+T1: β=−1.476, p=2.53×10(−10); executive function, FW: β=−1.276, p=1.46×10(−9); T1: β=−1.337, p=2.52×10(−7); FW+T1: β=−1.850, p=3.85×10(−17)) and longitudinal cognition (memory, FW: β=−0.091, p=4.62×10(−11); T1: β=−0.097, p=1.40×10(−8); FW+T1: β=−0.101, p=1.35×10(−11); executive function, FW: β=−0.125, p=1.20×10(−10); T1: β=−0.163, p=4.25×10(−12); FW+T1: β=−0.158, p=1.65×10(−14)). Our findings provide evidence that both T1-weighted MRI and dMRI measures improve brain age prediction and support predicted brain age as a sensitive biomarker of cognition and cognitive decline. Cold Spring Harbor Laboratory 2023-10-11 /pmc/articles/PMC10461919/ /pubmed/37645837 http://dx.doi.org/10.1101/2023.08.10.552494 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
Yang, Yisu
Sathe, Aditi
Schilling, Kurt
Shashikumar, Niranjana
Moore, Elizabeth
Dumitrescu, Logan
Pechman, Kimberly R.
Landman, Bennett A.
Gifford, Katherine A.
Hohman, Timothy J.
Jefferson, Angela L.
Archer, Derek B.
A deep neural network estimation of brain age is sensitive to cognitive impairment and decline
title A deep neural network estimation of brain age is sensitive to cognitive impairment and decline
title_full A deep neural network estimation of brain age is sensitive to cognitive impairment and decline
title_fullStr A deep neural network estimation of brain age is sensitive to cognitive impairment and decline
title_full_unstemmed A deep neural network estimation of brain age is sensitive to cognitive impairment and decline
title_short A deep neural network estimation of brain age is sensitive to cognitive impairment and decline
title_sort deep neural network estimation of brain age is sensitive to cognitive impairment and decline
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10461919/
https://www.ncbi.nlm.nih.gov/pubmed/37645837
http://dx.doi.org/10.1101/2023.08.10.552494
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