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LIFESPAN NEURODEGENERATION OF THE HUMAN BRAIN IN MULTIPLE SCLEROSIS
BACKGROUND: Atrophy related to Multiple Sclerosis (MS) has been found at the early stages of the disease. However, the archetype dynamic trajectories of the neurodegenerative process, even prior to clinical diagnosis, remain unknown. METHODS: We modeled the volumetric trajectories of brain structure...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055083/ https://www.ncbi.nlm.nih.gov/pubmed/36993352 http://dx.doi.org/10.1101/2023.03.14.532535 |
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author | Coupé, Pierrick Planche, Vincent Mansencal, Boris Kamroui, Reda A. Koubiyr, Ismail Manjon, José V. Tourdias, Thomas |
author_facet | Coupé, Pierrick Planche, Vincent Mansencal, Boris Kamroui, Reda A. Koubiyr, Ismail Manjon, José V. Tourdias, Thomas |
author_sort | Coupé, Pierrick |
collection | PubMed |
description | BACKGROUND: Atrophy related to Multiple Sclerosis (MS) has been found at the early stages of the disease. However, the archetype dynamic trajectories of the neurodegenerative process, even prior to clinical diagnosis, remain unknown. METHODS: We modeled the volumetric trajectories of brain structures across the entire lifespan using 40944 subjects (38295 healthy controls and 2649 MS patients). Then, we estimated the chronological progression of MS by assessing the divergence of lifespan trajectories between normal brain charts and MS brain charts. RESULTS: Chronologically, the first affected structure was the thalamus, then the putamen and the pallidum (3 years later), followed by the ventral diencephalon (7 years after thalamus) and finally the brainstem (9 years after thalamus). To a lesser extent, the anterior cingulate gyrus, insular cortex, occipital pole, caudate and hippocampus were impacted. Finally, the precuneus and accumbens nuclei exhibited a limited atrophy pattern. CONCLUSION: Subcortical atrophy was more pronounced than cortical atrophy. The thalamus was the most impacted structure with a very early divergence in life. It paves the way toward utilization of these lifespan models for future preclinical/prodromal prognosis and monitoring of MS. |
format | Online Article Text |
id | pubmed-10055083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-100550832023-03-30 LIFESPAN NEURODEGENERATION OF THE HUMAN BRAIN IN MULTIPLE SCLEROSIS Coupé, Pierrick Planche, Vincent Mansencal, Boris Kamroui, Reda A. Koubiyr, Ismail Manjon, José V. Tourdias, Thomas bioRxiv Article BACKGROUND: Atrophy related to Multiple Sclerosis (MS) has been found at the early stages of the disease. However, the archetype dynamic trajectories of the neurodegenerative process, even prior to clinical diagnosis, remain unknown. METHODS: We modeled the volumetric trajectories of brain structures across the entire lifespan using 40944 subjects (38295 healthy controls and 2649 MS patients). Then, we estimated the chronological progression of MS by assessing the divergence of lifespan trajectories between normal brain charts and MS brain charts. RESULTS: Chronologically, the first affected structure was the thalamus, then the putamen and the pallidum (3 years later), followed by the ventral diencephalon (7 years after thalamus) and finally the brainstem (9 years after thalamus). To a lesser extent, the anterior cingulate gyrus, insular cortex, occipital pole, caudate and hippocampus were impacted. Finally, the precuneus and accumbens nuclei exhibited a limited atrophy pattern. CONCLUSION: Subcortical atrophy was more pronounced than cortical atrophy. The thalamus was the most impacted structure with a very early divergence in life. It paves the way toward utilization of these lifespan models for future preclinical/prodromal prognosis and monitoring of MS. Cold Spring Harbor Laboratory 2023-03-14 /pmc/articles/PMC10055083/ /pubmed/36993352 http://dx.doi.org/10.1101/2023.03.14.532535 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 Coupé, Pierrick Planche, Vincent Mansencal, Boris Kamroui, Reda A. Koubiyr, Ismail Manjon, José V. Tourdias, Thomas LIFESPAN NEURODEGENERATION OF THE HUMAN BRAIN IN MULTIPLE SCLEROSIS |
title | LIFESPAN NEURODEGENERATION OF THE HUMAN BRAIN IN MULTIPLE SCLEROSIS |
title_full | LIFESPAN NEURODEGENERATION OF THE HUMAN BRAIN IN MULTIPLE SCLEROSIS |
title_fullStr | LIFESPAN NEURODEGENERATION OF THE HUMAN BRAIN IN MULTIPLE SCLEROSIS |
title_full_unstemmed | LIFESPAN NEURODEGENERATION OF THE HUMAN BRAIN IN MULTIPLE SCLEROSIS |
title_short | LIFESPAN NEURODEGENERATION OF THE HUMAN BRAIN IN MULTIPLE SCLEROSIS |
title_sort | lifespan neurodegeneration of the human brain in multiple sclerosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055083/ https://www.ncbi.nlm.nih.gov/pubmed/36993352 http://dx.doi.org/10.1101/2023.03.14.532535 |
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