Cargando…
Lifespan neurodegeneration of the human brain in multiple sclerosis
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. We modeled the volumetric trajectories of brain structures across the entire l...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619394/ https://www.ncbi.nlm.nih.gov/pubmed/37615064 http://dx.doi.org/10.1002/hbm.26464 |
_version_ | 1785129979692974080 |
---|---|
author | Coupé, Pierrick Planche, Vincent Mansencal, Boris Kamroui, Reda A. Koubiyr, Ismail Manjòn, José V. Tourdias, Thomas |
author_facet | Coupé, Pierrick Planche, Vincent Mansencal, Boris Kamroui, Reda A. Koubiyr, Ismail Manjòn, José V. Tourdias, Thomas |
author_sort | Coupé, Pierrick |
collection | PubMed |
description | 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. We modeled the volumetric trajectories of brain structures across the entire lifespan using 40,944 subjects (38,295 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. Chronologically, the first affected structure was the thalamus, then the putamen and the pallidum (around 4 years later), followed by the ventral diencephalon (around 7 years after thalamus) and finally the brainstem (around 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. Subcortical atrophy was more pronounced than cortical atrophy. The thalamus was the most impacted structure with a very early divergence in life. Our experiments showed that lifespan models of most impacted structures could be an important tool for future preclinical/prodromal prognosis and monitoring of MS. |
format | Online Article Text |
id | pubmed-10619394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106193942023-11-02 Lifespan neurodegeneration of the human brain in multiple sclerosis Coupé, Pierrick Planche, Vincent Mansencal, Boris Kamroui, Reda A. Koubiyr, Ismail Manjòn, José V. Tourdias, Thomas Hum Brain Mapp Research Articles 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. We modeled the volumetric trajectories of brain structures across the entire lifespan using 40,944 subjects (38,295 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. Chronologically, the first affected structure was the thalamus, then the putamen and the pallidum (around 4 years later), followed by the ventral diencephalon (around 7 years after thalamus) and finally the brainstem (around 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. Subcortical atrophy was more pronounced than cortical atrophy. The thalamus was the most impacted structure with a very early divergence in life. Our experiments showed that lifespan models of most impacted structures could be an important tool for future preclinical/prodromal prognosis and monitoring of MS. John Wiley & Sons, Inc. 2023-08-24 /pmc/articles/PMC10619394/ /pubmed/37615064 http://dx.doi.org/10.1002/hbm.26464 Text en © 2023 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) 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 Articles Coupé, Pierrick Planche, Vincent Mansencal, Boris Kamroui, Reda A. Koubiyr, Ismail Manjòn, 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 | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619394/ https://www.ncbi.nlm.nih.gov/pubmed/37615064 http://dx.doi.org/10.1002/hbm.26464 |
work_keys_str_mv | AT coupepierrick lifespanneurodegenerationofthehumanbraininmultiplesclerosis AT planchevincent lifespanneurodegenerationofthehumanbraininmultiplesclerosis AT mansencalboris lifespanneurodegenerationofthehumanbraininmultiplesclerosis AT kamrouiredaa lifespanneurodegenerationofthehumanbraininmultiplesclerosis AT koubiyrismail lifespanneurodegenerationofthehumanbraininmultiplesclerosis AT manjonjosev lifespanneurodegenerationofthehumanbraininmultiplesclerosis AT tourdiasthomas lifespanneurodegenerationofthehumanbraininmultiplesclerosis |