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Bridging structural and functional biomarkers in functional movement disorder using network mapping
BACKGROUND: There are gaps in our neurobiological understanding of functional movement disorder (FMD). OBJECTIVES: We investigated gray matter volumetric profiles in FMD, and related findings to resting‐state functional connectivity (rsFC) profiles using Human Connectome Project data. METHODS: Volu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120728/ https://www.ncbi.nlm.nih.gov/pubmed/35429407 http://dx.doi.org/10.1002/brb3.2576 |
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author | Sojka, Petr Slovák, Matěj Věchetová, Gabriela Jech, Robert Perez, David L. Serranová, Tereza |
author_facet | Sojka, Petr Slovák, Matěj Věchetová, Gabriela Jech, Robert Perez, David L. Serranová, Tereza |
author_sort | Sojka, Petr |
collection | PubMed |
description | BACKGROUND: There are gaps in our neurobiological understanding of functional movement disorder (FMD). OBJECTIVES: We investigated gray matter volumetric profiles in FMD, and related findings to resting‐state functional connectivity (rsFC) profiles using Human Connectome Project data. METHODS: Volumetric differences between 53 FMD patients and 50 controls were examined, as well as relationships between individual differences in FMD symptom severity and volumetric profiles. Atrophy network mapping was also used to probe whether FMD‐related structural alterations preferentially impacted brain areas with dense rsFC. RESULTS: Compared to controls without neurological comorbidities (albeit with mild depression and anxiety as a group), the FMD cohort did not show any volumetric differences. Across patients with FMD, individual differences in symptom severity negatively correlated with right supramarginal and bilateral superior temporal gyri volumes. These findings remained significant adjusting for FMD subtype or antidepressant use, but did not remain statistically significant adjusting for depression and anxiety scores. Symptom severity‐related structural alterations mapped onto regions with dense rsFC—identifying several disease epicenters in default mode, ventral attention, and salience networks. CONCLUSIONS: This study supports that FMD is a multinetwork disorder with an important role for the temporoparietal junction and its related connectivity in the pathophysiology of this condition. More research is needed to explore the intersection of functional neurological symptoms and mood. |
format | Online Article Text |
id | pubmed-9120728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91207282022-05-21 Bridging structural and functional biomarkers in functional movement disorder using network mapping Sojka, Petr Slovák, Matěj Věchetová, Gabriela Jech, Robert Perez, David L. Serranová, Tereza Brain Behav Original Articles BACKGROUND: There are gaps in our neurobiological understanding of functional movement disorder (FMD). OBJECTIVES: We investigated gray matter volumetric profiles in FMD, and related findings to resting‐state functional connectivity (rsFC) profiles using Human Connectome Project data. METHODS: Volumetric differences between 53 FMD patients and 50 controls were examined, as well as relationships between individual differences in FMD symptom severity and volumetric profiles. Atrophy network mapping was also used to probe whether FMD‐related structural alterations preferentially impacted brain areas with dense rsFC. RESULTS: Compared to controls without neurological comorbidities (albeit with mild depression and anxiety as a group), the FMD cohort did not show any volumetric differences. Across patients with FMD, individual differences in symptom severity negatively correlated with right supramarginal and bilateral superior temporal gyri volumes. These findings remained significant adjusting for FMD subtype or antidepressant use, but did not remain statistically significant adjusting for depression and anxiety scores. Symptom severity‐related structural alterations mapped onto regions with dense rsFC—identifying several disease epicenters in default mode, ventral attention, and salience networks. CONCLUSIONS: This study supports that FMD is a multinetwork disorder with an important role for the temporoparietal junction and its related connectivity in the pathophysiology of this condition. More research is needed to explore the intersection of functional neurological symptoms and mood. John Wiley and Sons Inc. 2022-04-16 /pmc/articles/PMC9120728/ /pubmed/35429407 http://dx.doi.org/10.1002/brb3.2576 Text en © 2022 The Authors. Brain and Behavior published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Sojka, Petr Slovák, Matěj Věchetová, Gabriela Jech, Robert Perez, David L. Serranová, Tereza Bridging structural and functional biomarkers in functional movement disorder using network mapping |
title | Bridging structural and functional biomarkers in functional movement disorder using network mapping |
title_full | Bridging structural and functional biomarkers in functional movement disorder using network mapping |
title_fullStr | Bridging structural and functional biomarkers in functional movement disorder using network mapping |
title_full_unstemmed | Bridging structural and functional biomarkers in functional movement disorder using network mapping |
title_short | Bridging structural and functional biomarkers in functional movement disorder using network mapping |
title_sort | bridging structural and functional biomarkers in functional movement disorder using network mapping |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120728/ https://www.ncbi.nlm.nih.gov/pubmed/35429407 http://dx.doi.org/10.1002/brb3.2576 |
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