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Using multiple short epochs optimises the stability of infant EEG connectivity parameters
Atypicalities in connectivity between brain regions have been implicated in a range of neurocognitive disorders. We require metrics to assess stable individual differences in connectivity in the developing brain, while facing the challenge of limited data quality and quantity. Here, we examine how v...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391718/ https://www.ncbi.nlm.nih.gov/pubmed/32728099 http://dx.doi.org/10.1038/s41598-020-68981-5 |
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author | Haartsen, Rianne van der Velde, Bauke Jones, Emily J. H. Johnson, Mark H. Kemner, Chantal |
author_facet | Haartsen, Rianne van der Velde, Bauke Jones, Emily J. H. Johnson, Mark H. Kemner, Chantal |
author_sort | Haartsen, Rianne |
collection | PubMed |
description | Atypicalities in connectivity between brain regions have been implicated in a range of neurocognitive disorders. We require metrics to assess stable individual differences in connectivity in the developing brain, while facing the challenge of limited data quality and quantity. Here, we examine how varying core processing parameters can optimise the test–retest reliability of EEG connectivity measures in infants. EEG was recorded twice with a 1-week interval between sessions in 10-month-olds. EEG alpha connectivity was measured across different epoch lengths and numbers, with the phase lag index (PLI) and debiased weighted PLI (dbWPLI), for both whole-head connectivity and graph theory metrics. We calculated intra-class correlations between sessions for infants with sufficient data for both sessions (N’s = 19–41, depending on the segmentation method). Reliability for the whole brain dbWPLI was higher across many short epochs, whereas reliability for the whole brain PLI was higher across fewer long epochs. However, the PLI is confounded by the number of available segments. Reliability was higher for whole brain connectivity than graph theory metrics. Thus, segmenting available data into a high number of short epochs and calculating the dbWPLI is most appropriate for characterising connectivity in populations with limited availability of EEG data. |
format | Online Article Text |
id | pubmed-7391718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73917182020-07-31 Using multiple short epochs optimises the stability of infant EEG connectivity parameters Haartsen, Rianne van der Velde, Bauke Jones, Emily J. H. Johnson, Mark H. Kemner, Chantal Sci Rep Article Atypicalities in connectivity between brain regions have been implicated in a range of neurocognitive disorders. We require metrics to assess stable individual differences in connectivity in the developing brain, while facing the challenge of limited data quality and quantity. Here, we examine how varying core processing parameters can optimise the test–retest reliability of EEG connectivity measures in infants. EEG was recorded twice with a 1-week interval between sessions in 10-month-olds. EEG alpha connectivity was measured across different epoch lengths and numbers, with the phase lag index (PLI) and debiased weighted PLI (dbWPLI), for both whole-head connectivity and graph theory metrics. We calculated intra-class correlations between sessions for infants with sufficient data for both sessions (N’s = 19–41, depending on the segmentation method). Reliability for the whole brain dbWPLI was higher across many short epochs, whereas reliability for the whole brain PLI was higher across fewer long epochs. However, the PLI is confounded by the number of available segments. Reliability was higher for whole brain connectivity than graph theory metrics. Thus, segmenting available data into a high number of short epochs and calculating the dbWPLI is most appropriate for characterising connectivity in populations with limited availability of EEG data. Nature Publishing Group UK 2020-07-29 /pmc/articles/PMC7391718/ /pubmed/32728099 http://dx.doi.org/10.1038/s41598-020-68981-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Haartsen, Rianne van der Velde, Bauke Jones, Emily J. H. Johnson, Mark H. Kemner, Chantal Using multiple short epochs optimises the stability of infant EEG connectivity parameters |
title | Using multiple short epochs optimises the stability of infant EEG connectivity parameters |
title_full | Using multiple short epochs optimises the stability of infant EEG connectivity parameters |
title_fullStr | Using multiple short epochs optimises the stability of infant EEG connectivity parameters |
title_full_unstemmed | Using multiple short epochs optimises the stability of infant EEG connectivity parameters |
title_short | Using multiple short epochs optimises the stability of infant EEG connectivity parameters |
title_sort | using multiple short epochs optimises the stability of infant eeg connectivity parameters |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391718/ https://www.ncbi.nlm.nih.gov/pubmed/32728099 http://dx.doi.org/10.1038/s41598-020-68981-5 |
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