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In vivo structural connectome of arousal and motor brainstem nuclei by 7 Tesla and 3 Tesla MRI

Brainstem nuclei are key participants in the generation and maintenance of arousal, which is a basic function that modulates wakefulness/sleep, autonomic responses, affect, attention, and consciousness. Their mechanism is based on diffuse pathways ascending from the brainstem to the thalamus, hypoth...

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Autores principales: García‐Gomar, María Guadalupe, Singh, Kavita, Cauzzo, Simone, Bianciardi, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9435015/
https://www.ncbi.nlm.nih.gov/pubmed/35633277
http://dx.doi.org/10.1002/hbm.25962
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author García‐Gomar, María Guadalupe
Singh, Kavita
Cauzzo, Simone
Bianciardi, Marta
author_facet García‐Gomar, María Guadalupe
Singh, Kavita
Cauzzo, Simone
Bianciardi, Marta
author_sort García‐Gomar, María Guadalupe
collection PubMed
description Brainstem nuclei are key participants in the generation and maintenance of arousal, which is a basic function that modulates wakefulness/sleep, autonomic responses, affect, attention, and consciousness. Their mechanism is based on diffuse pathways ascending from the brainstem to the thalamus, hypothalamus, basal forebrain and cortex. Several arousal brainstem nuclei also participate in motor functions that allow humans to respond and interact with the surrounding through a multipathway motor network. Yet, little is known about the structural connectivity of arousal and motor brainstem nuclei in living humans. This is due to the lack of appropriate tools able to accurately visualize brainstem nuclei in conventional imaging. Using a recently developed in vivo probabilistic brainstem nuclei atlas and 7 Tesla diffusion‐weighted images (DWI), we built the structural connectome of 18 arousal and motor brainstem nuclei in living humans (n = 19). Furthermore, to investigate the translatability of our findings to standard clinical MRI, we acquired 3 Tesla DWI on the same subjects, and measured the association of the connectome across scanners. For both arousal and motor circuits, our results showed high connectivity within brainstem nuclei, and with expected subcortical and cortical structures based on animal studies. The association between 3 Tesla and 7 Tesla connectivity values was good, especially within the brainstem. The resulting structural connectome might be used as a baseline to better understand arousal and motor functions in health and disease in humans.
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spelling pubmed-94350152022-09-08 In vivo structural connectome of arousal and motor brainstem nuclei by 7 Tesla and 3 Tesla MRI García‐Gomar, María Guadalupe Singh, Kavita Cauzzo, Simone Bianciardi, Marta Hum Brain Mapp Research Articles Brainstem nuclei are key participants in the generation and maintenance of arousal, which is a basic function that modulates wakefulness/sleep, autonomic responses, affect, attention, and consciousness. Their mechanism is based on diffuse pathways ascending from the brainstem to the thalamus, hypothalamus, basal forebrain and cortex. Several arousal brainstem nuclei also participate in motor functions that allow humans to respond and interact with the surrounding through a multipathway motor network. Yet, little is known about the structural connectivity of arousal and motor brainstem nuclei in living humans. This is due to the lack of appropriate tools able to accurately visualize brainstem nuclei in conventional imaging. Using a recently developed in vivo probabilistic brainstem nuclei atlas and 7 Tesla diffusion‐weighted images (DWI), we built the structural connectome of 18 arousal and motor brainstem nuclei in living humans (n = 19). Furthermore, to investigate the translatability of our findings to standard clinical MRI, we acquired 3 Tesla DWI on the same subjects, and measured the association of the connectome across scanners. For both arousal and motor circuits, our results showed high connectivity within brainstem nuclei, and with expected subcortical and cortical structures based on animal studies. The association between 3 Tesla and 7 Tesla connectivity values was good, especially within the brainstem. The resulting structural connectome might be used as a baseline to better understand arousal and motor functions in health and disease in humans. John Wiley & Sons, Inc. 2022-05-28 /pmc/articles/PMC9435015/ /pubmed/35633277 http://dx.doi.org/10.1002/hbm.25962 Text en © 2022 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
García‐Gomar, María Guadalupe
Singh, Kavita
Cauzzo, Simone
Bianciardi, Marta
In vivo structural connectome of arousal and motor brainstem nuclei by 7 Tesla and 3 Tesla MRI
title In vivo structural connectome of arousal and motor brainstem nuclei by 7 Tesla and 3 Tesla MRI
title_full In vivo structural connectome of arousal and motor brainstem nuclei by 7 Tesla and 3 Tesla MRI
title_fullStr In vivo structural connectome of arousal and motor brainstem nuclei by 7 Tesla and 3 Tesla MRI
title_full_unstemmed In vivo structural connectome of arousal and motor brainstem nuclei by 7 Tesla and 3 Tesla MRI
title_short In vivo structural connectome of arousal and motor brainstem nuclei by 7 Tesla and 3 Tesla MRI
title_sort in vivo structural connectome of arousal and motor brainstem nuclei by 7 tesla and 3 tesla mri
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9435015/
https://www.ncbi.nlm.nih.gov/pubmed/35633277
http://dx.doi.org/10.1002/hbm.25962
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