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Regional expression of the MAPT gene is associated with loss of hubs in brain networks and cognitive impairment in Parkinson disease and progressive supranuclear palsy

Abnormalities of tau protein are central to the pathogenesis of progressive supranuclear palsy, whereas haplotype variation of the tau gene MAPT influences the risk of Parkinson disease and Parkinson's disease dementia. We assessed whether regional MAPT expression might be associated with selec...

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Autores principales: Rittman, Timothy, Rubinov, Mikail, Vértes, Petra E., Patel, Ameera X., Ginestet, Cedric E., Ghosh, Boyd C.P., Barker, Roger A., Spillantini, Maria Grazia, Bullmore, Edward T., Rowe, James B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096886/
https://www.ncbi.nlm.nih.gov/pubmed/27697694
http://dx.doi.org/10.1016/j.neurobiolaging.2016.09.001
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author Rittman, Timothy
Rubinov, Mikail
Vértes, Petra E.
Patel, Ameera X.
Ginestet, Cedric E.
Ghosh, Boyd C.P.
Barker, Roger A.
Spillantini, Maria Grazia
Bullmore, Edward T.
Rowe, James B.
author_facet Rittman, Timothy
Rubinov, Mikail
Vértes, Petra E.
Patel, Ameera X.
Ginestet, Cedric E.
Ghosh, Boyd C.P.
Barker, Roger A.
Spillantini, Maria Grazia
Bullmore, Edward T.
Rowe, James B.
author_sort Rittman, Timothy
collection PubMed
description Abnormalities of tau protein are central to the pathogenesis of progressive supranuclear palsy, whereas haplotype variation of the tau gene MAPT influences the risk of Parkinson disease and Parkinson's disease dementia. We assessed whether regional MAPT expression might be associated with selective vulnerability of global brain networks to neurodegenerative pathology. Using task-free functional magnetic resonance imaging in progressive supranuclear palsy, Parkinson disease, and healthy subjects (n = 128), we examined functional brain networks and measured the connection strength between 471 gray matter regions. We obtained MAPT and SNCA microarray expression data in healthy subjects from the Allen brain atlas. Regional connectivity varied according to the normal expression of MAPT. The regional expression of MAPT correlated with the proportionate loss of regional connectivity in Parkinson's disease. Executive cognition was impaired in proportion to the loss of hub connectivity. These effects were not seen with SNCA, suggesting that alpha-synuclein pathology is not mediated through global network properties. The results establish a link between regional MAPT expression and selective vulnerability of functional brain networks to neurodegeneration.
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spelling pubmed-50968862016-12-01 Regional expression of the MAPT gene is associated with loss of hubs in brain networks and cognitive impairment in Parkinson disease and progressive supranuclear palsy Rittman, Timothy Rubinov, Mikail Vértes, Petra E. Patel, Ameera X. Ginestet, Cedric E. Ghosh, Boyd C.P. Barker, Roger A. Spillantini, Maria Grazia Bullmore, Edward T. Rowe, James B. Neurobiol Aging Regular Article Abnormalities of tau protein are central to the pathogenesis of progressive supranuclear palsy, whereas haplotype variation of the tau gene MAPT influences the risk of Parkinson disease and Parkinson's disease dementia. We assessed whether regional MAPT expression might be associated with selective vulnerability of global brain networks to neurodegenerative pathology. Using task-free functional magnetic resonance imaging in progressive supranuclear palsy, Parkinson disease, and healthy subjects (n = 128), we examined functional brain networks and measured the connection strength between 471 gray matter regions. We obtained MAPT and SNCA microarray expression data in healthy subjects from the Allen brain atlas. Regional connectivity varied according to the normal expression of MAPT. The regional expression of MAPT correlated with the proportionate loss of regional connectivity in Parkinson's disease. Executive cognition was impaired in proportion to the loss of hub connectivity. These effects were not seen with SNCA, suggesting that alpha-synuclein pathology is not mediated through global network properties. The results establish a link between regional MAPT expression and selective vulnerability of functional brain networks to neurodegeneration. Elsevier 2016-12 /pmc/articles/PMC5096886/ /pubmed/27697694 http://dx.doi.org/10.1016/j.neurobiolaging.2016.09.001 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Article
Rittman, Timothy
Rubinov, Mikail
Vértes, Petra E.
Patel, Ameera X.
Ginestet, Cedric E.
Ghosh, Boyd C.P.
Barker, Roger A.
Spillantini, Maria Grazia
Bullmore, Edward T.
Rowe, James B.
Regional expression of the MAPT gene is associated with loss of hubs in brain networks and cognitive impairment in Parkinson disease and progressive supranuclear palsy
title Regional expression of the MAPT gene is associated with loss of hubs in brain networks and cognitive impairment in Parkinson disease and progressive supranuclear palsy
title_full Regional expression of the MAPT gene is associated with loss of hubs in brain networks and cognitive impairment in Parkinson disease and progressive supranuclear palsy
title_fullStr Regional expression of the MAPT gene is associated with loss of hubs in brain networks and cognitive impairment in Parkinson disease and progressive supranuclear palsy
title_full_unstemmed Regional expression of the MAPT gene is associated with loss of hubs in brain networks and cognitive impairment in Parkinson disease and progressive supranuclear palsy
title_short Regional expression of the MAPT gene is associated with loss of hubs in brain networks and cognitive impairment in Parkinson disease and progressive supranuclear palsy
title_sort regional expression of the mapt gene is associated with loss of hubs in brain networks and cognitive impairment in parkinson disease and progressive supranuclear palsy
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096886/
https://www.ncbi.nlm.nih.gov/pubmed/27697694
http://dx.doi.org/10.1016/j.neurobiolaging.2016.09.001
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