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Cortical lesions causing loss of consciousness are anticorrelated with the dorsal brainstem

Brain lesions can provide unique insight into the neuroanatomical substrate of human consciousness. For example, brainstem lesions causing coma map to a specific region of the tegmentum. Whether specific lesion locations outside the brainstem are associated with loss of consciousness (LOC) remains u...

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Autores principales: Snider, Samuel B., Hsu, Joey, Darby, R. Ryan, Cooke, Danielle, Fischer, David, Cohen, Alexander L., Grafman, Jordan H., Fox, Michael D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268053/
https://www.ncbi.nlm.nih.gov/pubmed/31904898
http://dx.doi.org/10.1002/hbm.24892
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author Snider, Samuel B.
Hsu, Joey
Darby, R. Ryan
Cooke, Danielle
Fischer, David
Cohen, Alexander L.
Grafman, Jordan H.
Fox, Michael D.
author_facet Snider, Samuel B.
Hsu, Joey
Darby, R. Ryan
Cooke, Danielle
Fischer, David
Cohen, Alexander L.
Grafman, Jordan H.
Fox, Michael D.
author_sort Snider, Samuel B.
collection PubMed
description Brain lesions can provide unique insight into the neuroanatomical substrate of human consciousness. For example, brainstem lesions causing coma map to a specific region of the tegmentum. Whether specific lesion locations outside the brainstem are associated with loss of consciousness (LOC) remains unclear. Here, we investigate the topography of cortical lesions causing prolonged LOC (N = 16), transient LOC (N = 91), or no LOC (N = 64). Using standard voxel lesion symptom mapping, no focus of brain damage was associated with LOC. Next, we computed the network of brain regions functionally connected to each lesion location using a large normative connectome dataset (N = 1,000). This technique, termed lesion network mapping, can test whether lesions causing LOC map to a connected brain circuit rather than one brain region. Connectivity between cortical lesion locations and an a priori coma‐specific region of brainstem tegmentum was an independent predictor of LOC (B = 1.2, p = .004). Connectivity to the dorsal brainstem was the only predictor of LOC in a whole‐brain voxel‐wise analysis. This relationship was driven by anticorrelation (negative correlation) between lesion locations and the dorsal brainstem. The map of regions anticorrelated to the dorsal brainstem thus defines a distributed brain circuit that, when damaged, is most likely to cause LOC. This circuit showed a slight posterior predominance and had peaks in the bilateral claustrum. Our results suggest that cortical lesions causing LOC map to a connected brain circuit, linking cortical lesions that disrupt consciousness to brainstem sites that maintain arousal.
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spelling pubmed-72680532020-06-12 Cortical lesions causing loss of consciousness are anticorrelated with the dorsal brainstem Snider, Samuel B. Hsu, Joey Darby, R. Ryan Cooke, Danielle Fischer, David Cohen, Alexander L. Grafman, Jordan H. Fox, Michael D. Hum Brain Mapp Research Articles Brain lesions can provide unique insight into the neuroanatomical substrate of human consciousness. For example, brainstem lesions causing coma map to a specific region of the tegmentum. Whether specific lesion locations outside the brainstem are associated with loss of consciousness (LOC) remains unclear. Here, we investigate the topography of cortical lesions causing prolonged LOC (N = 16), transient LOC (N = 91), or no LOC (N = 64). Using standard voxel lesion symptom mapping, no focus of brain damage was associated with LOC. Next, we computed the network of brain regions functionally connected to each lesion location using a large normative connectome dataset (N = 1,000). This technique, termed lesion network mapping, can test whether lesions causing LOC map to a connected brain circuit rather than one brain region. Connectivity between cortical lesion locations and an a priori coma‐specific region of brainstem tegmentum was an independent predictor of LOC (B = 1.2, p = .004). Connectivity to the dorsal brainstem was the only predictor of LOC in a whole‐brain voxel‐wise analysis. This relationship was driven by anticorrelation (negative correlation) between lesion locations and the dorsal brainstem. The map of regions anticorrelated to the dorsal brainstem thus defines a distributed brain circuit that, when damaged, is most likely to cause LOC. This circuit showed a slight posterior predominance and had peaks in the bilateral claustrum. Our results suggest that cortical lesions causing LOC map to a connected brain circuit, linking cortical lesions that disrupt consciousness to brainstem sites that maintain arousal. John Wiley & Sons, Inc. 2020-01-06 /pmc/articles/PMC7268053/ /pubmed/31904898 http://dx.doi.org/10.1002/hbm.24892 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Snider, Samuel B.
Hsu, Joey
Darby, R. Ryan
Cooke, Danielle
Fischer, David
Cohen, Alexander L.
Grafman, Jordan H.
Fox, Michael D.
Cortical lesions causing loss of consciousness are anticorrelated with the dorsal brainstem
title Cortical lesions causing loss of consciousness are anticorrelated with the dorsal brainstem
title_full Cortical lesions causing loss of consciousness are anticorrelated with the dorsal brainstem
title_fullStr Cortical lesions causing loss of consciousness are anticorrelated with the dorsal brainstem
title_full_unstemmed Cortical lesions causing loss of consciousness are anticorrelated with the dorsal brainstem
title_short Cortical lesions causing loss of consciousness are anticorrelated with the dorsal brainstem
title_sort cortical lesions causing loss of consciousness are anticorrelated with the dorsal brainstem
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7268053/
https://www.ncbi.nlm.nih.gov/pubmed/31904898
http://dx.doi.org/10.1002/hbm.24892
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