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State-dependent signatures of anti-N-methyl-d-aspartate receptor encephalitis
Traditional static functional connectivity analyses have shown distinct functional network alterations in patients with anti-N-methyl-d-aspartate receptor encephalitis. Here, we use a dynamic functional connectivity approach that increases the temporal resolution of connectivity analyses from minute...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833311/ https://www.ncbi.nlm.nih.gov/pubmed/35169701 http://dx.doi.org/10.1093/braincomms/fcab298 |
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author | von Schwanenflug, Nina Krohn, Stephan Heine, Josephine Paul, Friedemann Prüss, Harald Finke, Carsten |
author_facet | von Schwanenflug, Nina Krohn, Stephan Heine, Josephine Paul, Friedemann Prüss, Harald Finke, Carsten |
author_sort | von Schwanenflug, Nina |
collection | PubMed |
description | Traditional static functional connectivity analyses have shown distinct functional network alterations in patients with anti-N-methyl-d-aspartate receptor encephalitis. Here, we use a dynamic functional connectivity approach that increases the temporal resolution of connectivity analyses from minutes to seconds. We hereby explore the spatiotemporal variability of large-scale brain network activity in anti-N-methyl-d-aspartate receptor encephalitis and assess the discriminatory power of functional brain states in a supervised classification approach. We included resting-state functional magnetic resonance imaging data from 57 patients and 61 controls to extract four discrete connectivity states and assess state-wise group differences in functional connectivity, dwell time, transition frequency, fraction time and occurrence rate. Additionally, for each state, logistic regression models with embedded feature selection were trained to predict group status in a leave-one-out cross-validation scheme. Compared to controls, patients exhibited diverging dynamic functional connectivity patterns in three out of four states mainly encompassing the default-mode network and frontal areas. This was accompanied by a characteristic shift in the dwell time pattern and higher volatility of state transitions in patients. Moreover, dynamic functional connectivity measures were associated with disease severity and positive and negative schizophrenia-like symptoms. Predictive power was highest in dynamic functional connectivity models and outperformed static analyses, reaching up to 78.6% classification accuracy. By applying time-resolved analyses, we disentangle state-specific functional connectivity impairments and characteristic changes in temporal dynamics not detected in static analyses, offering new perspectives on the functional reorganization underlying anti-N-methyl-d-aspartate receptor encephalitis. Finally, the correlation of dynamic functional connectivity measures with disease symptoms and severity demonstrates a clinical relevance of spatiotemporal connectivity dynamics in anti-N-methyl-d-aspartate receptor encephalitis. |
format | Online Article Text |
id | pubmed-8833311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-88333112022-02-14 State-dependent signatures of anti-N-methyl-d-aspartate receptor encephalitis von Schwanenflug, Nina Krohn, Stephan Heine, Josephine Paul, Friedemann Prüss, Harald Finke, Carsten Brain Commun Original Article Traditional static functional connectivity analyses have shown distinct functional network alterations in patients with anti-N-methyl-d-aspartate receptor encephalitis. Here, we use a dynamic functional connectivity approach that increases the temporal resolution of connectivity analyses from minutes to seconds. We hereby explore the spatiotemporal variability of large-scale brain network activity in anti-N-methyl-d-aspartate receptor encephalitis and assess the discriminatory power of functional brain states in a supervised classification approach. We included resting-state functional magnetic resonance imaging data from 57 patients and 61 controls to extract four discrete connectivity states and assess state-wise group differences in functional connectivity, dwell time, transition frequency, fraction time and occurrence rate. Additionally, for each state, logistic regression models with embedded feature selection were trained to predict group status in a leave-one-out cross-validation scheme. Compared to controls, patients exhibited diverging dynamic functional connectivity patterns in three out of four states mainly encompassing the default-mode network and frontal areas. This was accompanied by a characteristic shift in the dwell time pattern and higher volatility of state transitions in patients. Moreover, dynamic functional connectivity measures were associated with disease severity and positive and negative schizophrenia-like symptoms. Predictive power was highest in dynamic functional connectivity models and outperformed static analyses, reaching up to 78.6% classification accuracy. By applying time-resolved analyses, we disentangle state-specific functional connectivity impairments and characteristic changes in temporal dynamics not detected in static analyses, offering new perspectives on the functional reorganization underlying anti-N-methyl-d-aspartate receptor encephalitis. Finally, the correlation of dynamic functional connectivity measures with disease symptoms and severity demonstrates a clinical relevance of spatiotemporal connectivity dynamics in anti-N-methyl-d-aspartate receptor encephalitis. Oxford University Press 2022-02-01 /pmc/articles/PMC8833311/ /pubmed/35169701 http://dx.doi.org/10.1093/braincomms/fcab298 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article von Schwanenflug, Nina Krohn, Stephan Heine, Josephine Paul, Friedemann Prüss, Harald Finke, Carsten State-dependent signatures of anti-N-methyl-d-aspartate receptor encephalitis |
title | State-dependent signatures of anti-N-methyl-d-aspartate receptor encephalitis |
title_full | State-dependent signatures of anti-N-methyl-d-aspartate receptor encephalitis |
title_fullStr | State-dependent signatures of anti-N-methyl-d-aspartate receptor encephalitis |
title_full_unstemmed | State-dependent signatures of anti-N-methyl-d-aspartate receptor encephalitis |
title_short | State-dependent signatures of anti-N-methyl-d-aspartate receptor encephalitis |
title_sort | state-dependent signatures of anti-n-methyl-d-aspartate receptor encephalitis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8833311/ https://www.ncbi.nlm.nih.gov/pubmed/35169701 http://dx.doi.org/10.1093/braincomms/fcab298 |
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