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Structural brain abnormalities in postural tachycardia syndrome: A VBM-DARTEL study

Postural tachycardia syndrome (PoTS), a form of dysautonomia, is characterized by orthostatic intolerance, and is frequently accompanied by a range of symptoms including palpitations, lightheadedness, clouding of thought, blurred vision, fatigue, anxiety, and depression. Although the estimated preva...

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Autores principales: Umeda, Satoshi, Harrison, Neil A., Gray, Marcus A., Mathias, Christopher J., Critchley, Hugo D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362313/
https://www.ncbi.nlm.nih.gov/pubmed/25852449
http://dx.doi.org/10.3389/fnins.2015.00034
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author Umeda, Satoshi
Harrison, Neil A.
Gray, Marcus A.
Mathias, Christopher J.
Critchley, Hugo D.
author_facet Umeda, Satoshi
Harrison, Neil A.
Gray, Marcus A.
Mathias, Christopher J.
Critchley, Hugo D.
author_sort Umeda, Satoshi
collection PubMed
description Postural tachycardia syndrome (PoTS), a form of dysautonomia, is characterized by orthostatic intolerance, and is frequently accompanied by a range of symptoms including palpitations, lightheadedness, clouding of thought, blurred vision, fatigue, anxiety, and depression. Although the estimated prevalence of PoTS is approximately 5–10 times as common as the better-known condition orthostatic hypotension, the neural substrates of the syndrome are poorly characterized. In the present study, we used magnetic resonance imaging (MRI) with voxel-based morphometry (VBM) applying the diffeomorphic anatomical registration through exponentiated lie algebra (DARTEL) procedure to examine variation in regional brain structure associated with PoTS. We recruited 11 patients with established PoTS and 23 age-matched normal controls. Group comparison of gray matter volume revealed diminished gray matter volume within the left anterior insula, right middle frontal gyrus and right cingulate gyrus in the PoTS group. We also observed lower white matter volume beneath the precentral gyrus and paracentral lobule, right pre- and post-central gyrus, paracentral lobule and superior frontal gyrus in PoTS patients. Subsequent ROI analyses revealed significant negative correlations between left insula volume and trait anxiety and depression scores. Together, these findings of structural differences, particularly within insular and cingulate components of the salience network, suggest a link between dysregulated physiological reactions arising from compromised central autonomic control (and interoceptive representation) and increased vulnerability to psychiatric symptoms in PoTS patients.
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spelling pubmed-43623132015-04-07 Structural brain abnormalities in postural tachycardia syndrome: A VBM-DARTEL study Umeda, Satoshi Harrison, Neil A. Gray, Marcus A. Mathias, Christopher J. Critchley, Hugo D. Front Neurosci Neurology Postural tachycardia syndrome (PoTS), a form of dysautonomia, is characterized by orthostatic intolerance, and is frequently accompanied by a range of symptoms including palpitations, lightheadedness, clouding of thought, blurred vision, fatigue, anxiety, and depression. Although the estimated prevalence of PoTS is approximately 5–10 times as common as the better-known condition orthostatic hypotension, the neural substrates of the syndrome are poorly characterized. In the present study, we used magnetic resonance imaging (MRI) with voxel-based morphometry (VBM) applying the diffeomorphic anatomical registration through exponentiated lie algebra (DARTEL) procedure to examine variation in regional brain structure associated with PoTS. We recruited 11 patients with established PoTS and 23 age-matched normal controls. Group comparison of gray matter volume revealed diminished gray matter volume within the left anterior insula, right middle frontal gyrus and right cingulate gyrus in the PoTS group. We also observed lower white matter volume beneath the precentral gyrus and paracentral lobule, right pre- and post-central gyrus, paracentral lobule and superior frontal gyrus in PoTS patients. Subsequent ROI analyses revealed significant negative correlations between left insula volume and trait anxiety and depression scores. Together, these findings of structural differences, particularly within insular and cingulate components of the salience network, suggest a link between dysregulated physiological reactions arising from compromised central autonomic control (and interoceptive representation) and increased vulnerability to psychiatric symptoms in PoTS patients. Frontiers Media S.A. 2015-03-17 /pmc/articles/PMC4362313/ /pubmed/25852449 http://dx.doi.org/10.3389/fnins.2015.00034 Text en Copyright © 2015 Umeda, Harrison, Gray, Mathias and Critchley. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Umeda, Satoshi
Harrison, Neil A.
Gray, Marcus A.
Mathias, Christopher J.
Critchley, Hugo D.
Structural brain abnormalities in postural tachycardia syndrome: A VBM-DARTEL study
title Structural brain abnormalities in postural tachycardia syndrome: A VBM-DARTEL study
title_full Structural brain abnormalities in postural tachycardia syndrome: A VBM-DARTEL study
title_fullStr Structural brain abnormalities in postural tachycardia syndrome: A VBM-DARTEL study
title_full_unstemmed Structural brain abnormalities in postural tachycardia syndrome: A VBM-DARTEL study
title_short Structural brain abnormalities in postural tachycardia syndrome: A VBM-DARTEL study
title_sort structural brain abnormalities in postural tachycardia syndrome: a vbm-dartel study
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4362313/
https://www.ncbi.nlm.nih.gov/pubmed/25852449
http://dx.doi.org/10.3389/fnins.2015.00034
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