Cargando…
Juvenile myoclonic epilepsy shows increased posterior theta, and reduced sensorimotor beta resting connectivity
BACKGROUND: Widespread structural and functional brain network changes have been shown in Juvenile Myoclonic Epilepsy (JME) despite normal clinical neuroimaging. We sought to better define these changes using magnetoencephalography (MEG) and source space connectivity analysis for optimal neurophysio...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Publishers
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7684644/ https://www.ncbi.nlm.nih.gov/pubmed/32335503 http://dx.doi.org/10.1016/j.eplepsyres.2020.106324 |
_version_ | 1783613044221280256 |
---|---|
author | Routley, Bethany Shaw, Alexander Muthukumaraswamy, Suresh D Singh, Krish D Hamandi, Khalid |
author_facet | Routley, Bethany Shaw, Alexander Muthukumaraswamy, Suresh D Singh, Krish D Hamandi, Khalid |
author_sort | Routley, Bethany |
collection | PubMed |
description | BACKGROUND: Widespread structural and functional brain network changes have been shown in Juvenile Myoclonic Epilepsy (JME) despite normal clinical neuroimaging. We sought to better define these changes using magnetoencephalography (MEG) and source space connectivity analysis for optimal neurophysiological and anatomical localisation. METHODS: We consecutively recruited 26 patients with JME who underwent resting state MEG recording, along with 26 age-and-sex matched controls. Whole brain connectivity was determined through correlation of Automated Anatomical Labelling (AAL) atlas source space MEG timeseries in conventional frequency bands of interest delta (1−4 Hz), theta (4−8 Hz), alpha (8−13 Hz), beta (13−30 Hz) and gamma (40−60 Hz). We used a Linearly Constrained Minimum Variance (LCMV) beamformer to extract voxel wise time series of ‘virtual sensors’ for the desired frequency bands, followed by connectivity analysis using correlation between frequency- and node-specific power fluctuations, for the voxel maxima in each AAL atlas label, correcting for noise, potentially spurious connections and multiple comparisons. RESULTS: We found increased connectivity in the theta band in posterior brain regions, surviving statistical correction for multiple comparisons (corrected p < 0.05), and decreased connectivity in the beta band in sensorimotor cortex, between right pre- and post- central gyrus (p < 0.05) in JME compared to controls. CONCLUSIONS: Altered resting-state MEG connectivity in JME comprised increased connectivity in posterior theta – the frequency band associated with long range connections affecting attention and arousal - and decreased beta-band sensorimotor connectivity. These findings likely relate to altered regulation of the sensorimotor network and seizure prone states in JME. |
format | Online Article Text |
id | pubmed-7684644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-76846442020-12-07 Juvenile myoclonic epilepsy shows increased posterior theta, and reduced sensorimotor beta resting connectivity Routley, Bethany Shaw, Alexander Muthukumaraswamy, Suresh D Singh, Krish D Hamandi, Khalid Epilepsy Res Article BACKGROUND: Widespread structural and functional brain network changes have been shown in Juvenile Myoclonic Epilepsy (JME) despite normal clinical neuroimaging. We sought to better define these changes using magnetoencephalography (MEG) and source space connectivity analysis for optimal neurophysiological and anatomical localisation. METHODS: We consecutively recruited 26 patients with JME who underwent resting state MEG recording, along with 26 age-and-sex matched controls. Whole brain connectivity was determined through correlation of Automated Anatomical Labelling (AAL) atlas source space MEG timeseries in conventional frequency bands of interest delta (1−4 Hz), theta (4−8 Hz), alpha (8−13 Hz), beta (13−30 Hz) and gamma (40−60 Hz). We used a Linearly Constrained Minimum Variance (LCMV) beamformer to extract voxel wise time series of ‘virtual sensors’ for the desired frequency bands, followed by connectivity analysis using correlation between frequency- and node-specific power fluctuations, for the voxel maxima in each AAL atlas label, correcting for noise, potentially spurious connections and multiple comparisons. RESULTS: We found increased connectivity in the theta band in posterior brain regions, surviving statistical correction for multiple comparisons (corrected p < 0.05), and decreased connectivity in the beta band in sensorimotor cortex, between right pre- and post- central gyrus (p < 0.05) in JME compared to controls. CONCLUSIONS: Altered resting-state MEG connectivity in JME comprised increased connectivity in posterior theta – the frequency band associated with long range connections affecting attention and arousal - and decreased beta-band sensorimotor connectivity. These findings likely relate to altered regulation of the sensorimotor network and seizure prone states in JME. Elsevier Science Publishers 2020-07 /pmc/articles/PMC7684644/ /pubmed/32335503 http://dx.doi.org/10.1016/j.eplepsyres.2020.106324 Text en © 2020 The Authors. Published by Elsevier B.V. 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 | Article Routley, Bethany Shaw, Alexander Muthukumaraswamy, Suresh D Singh, Krish D Hamandi, Khalid Juvenile myoclonic epilepsy shows increased posterior theta, and reduced sensorimotor beta resting connectivity |
title | Juvenile myoclonic epilepsy shows increased posterior theta, and reduced sensorimotor beta resting connectivity |
title_full | Juvenile myoclonic epilepsy shows increased posterior theta, and reduced sensorimotor beta resting connectivity |
title_fullStr | Juvenile myoclonic epilepsy shows increased posterior theta, and reduced sensorimotor beta resting connectivity |
title_full_unstemmed | Juvenile myoclonic epilepsy shows increased posterior theta, and reduced sensorimotor beta resting connectivity |
title_short | Juvenile myoclonic epilepsy shows increased posterior theta, and reduced sensorimotor beta resting connectivity |
title_sort | juvenile myoclonic epilepsy shows increased posterior theta, and reduced sensorimotor beta resting connectivity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7684644/ https://www.ncbi.nlm.nih.gov/pubmed/32335503 http://dx.doi.org/10.1016/j.eplepsyres.2020.106324 |
work_keys_str_mv | AT routleybethany juvenilemyoclonicepilepsyshowsincreasedposteriorthetaandreducedsensorimotorbetarestingconnectivity AT shawalexander juvenilemyoclonicepilepsyshowsincreasedposteriorthetaandreducedsensorimotorbetarestingconnectivity AT muthukumaraswamysureshd juvenilemyoclonicepilepsyshowsincreasedposteriorthetaandreducedsensorimotorbetarestingconnectivity AT singhkrishd juvenilemyoclonicepilepsyshowsincreasedposteriorthetaandreducedsensorimotorbetarestingconnectivity AT hamandikhalid juvenilemyoclonicepilepsyshowsincreasedposteriorthetaandreducedsensorimotorbetarestingconnectivity |