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Sensitive and reproducible MEG resting-state metrics of functional connectivity in Alzheimer’s disease
BACKGROUND: Analysis of functional brain networks in Alzheimer’s disease (AD) has been hampered by a lack of reproducible, yet valid metrics of functional connectivity (FC). This study aimed to assess both the sensitivity and reproducibility of the corrected amplitude envelope correlation (AEC-c) an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881826/ https://www.ncbi.nlm.nih.gov/pubmed/35219327 http://dx.doi.org/10.1186/s13195-022-00970-4 |
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author | Schoonhoven, Deborah N. Briels, Casper T. Hillebrand, Arjan Scheltens, Philip Stam, Cornelis J. Gouw, Alida A. |
author_facet | Schoonhoven, Deborah N. Briels, Casper T. Hillebrand, Arjan Scheltens, Philip Stam, Cornelis J. Gouw, Alida A. |
author_sort | Schoonhoven, Deborah N. |
collection | PubMed |
description | BACKGROUND: Analysis of functional brain networks in Alzheimer’s disease (AD) has been hampered by a lack of reproducible, yet valid metrics of functional connectivity (FC). This study aimed to assess both the sensitivity and reproducibility of the corrected amplitude envelope correlation (AEC-c) and phase lag index (PLI), two metrics of FC that are insensitive to the effects of volume conduction and field spread, in two separate cohorts of patients with dementia due to AD versus healthy elderly controls. METHODS: Subjects with a clinical diagnosis of AD dementia with biomarker proof, and a control group of subjective cognitive decline (SCD), underwent two 5-min resting-state MEG recordings. Data consisted of a test (AD = 28; SCD = 29) and validation (AD = 29; SCD = 27) cohort. Time-series were estimated for 90 regions of interest (ROIs) in the automated anatomical labelling (AAL) atlas. For each of five canonical frequency bands, the AEC-c and PLI were calculated between all 90 ROIs, and connections were averaged per ROI. General linear models were constructed to compare the global FC differences between the groups, assess the reproducibility, and evaluate the effects of age and relative power. Reproducibility of the regional FC differences was assessed using the Mann-Whitney U tests, with correction for multiple testing using the false discovery rate (FDR). RESULTS: The AEC-c showed significantly and reproducibly lower global FC for the AD group compared to SCD, in the alpha (8–13 Hz) and beta (13–30 Hz) bands, while the PLI revealed reproducibly lower FC for the AD group in the delta (0.5–4 Hz) band and higher FC for the theta (4–8 Hz) band. Regionally, the beta band AEC-c showed reproducibility for almost all ROIs (except for 13 ROIs in the frontal and temporal lobes). For the other bands, the AEC-c and PLI did not show regional reproducibility after FDR correction. The theta band PLI was susceptible to the effect of relative power. CONCLUSION: For MEG, the AEC-c is a sensitive and reproducible metric, able to distinguish FC differences between patients with AD dementia and cognitively healthy controls. These two measures likely reflect different aspects of neural activity and show differential sensitivity to changes in neural dynamics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13195-022-00970-4. |
format | Online Article Text |
id | pubmed-8881826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88818262022-02-28 Sensitive and reproducible MEG resting-state metrics of functional connectivity in Alzheimer’s disease Schoonhoven, Deborah N. Briels, Casper T. Hillebrand, Arjan Scheltens, Philip Stam, Cornelis J. Gouw, Alida A. Alzheimers Res Ther Research BACKGROUND: Analysis of functional brain networks in Alzheimer’s disease (AD) has been hampered by a lack of reproducible, yet valid metrics of functional connectivity (FC). This study aimed to assess both the sensitivity and reproducibility of the corrected amplitude envelope correlation (AEC-c) and phase lag index (PLI), two metrics of FC that are insensitive to the effects of volume conduction and field spread, in two separate cohorts of patients with dementia due to AD versus healthy elderly controls. METHODS: Subjects with a clinical diagnosis of AD dementia with biomarker proof, and a control group of subjective cognitive decline (SCD), underwent two 5-min resting-state MEG recordings. Data consisted of a test (AD = 28; SCD = 29) and validation (AD = 29; SCD = 27) cohort. Time-series were estimated for 90 regions of interest (ROIs) in the automated anatomical labelling (AAL) atlas. For each of five canonical frequency bands, the AEC-c and PLI were calculated between all 90 ROIs, and connections were averaged per ROI. General linear models were constructed to compare the global FC differences between the groups, assess the reproducibility, and evaluate the effects of age and relative power. Reproducibility of the regional FC differences was assessed using the Mann-Whitney U tests, with correction for multiple testing using the false discovery rate (FDR). RESULTS: The AEC-c showed significantly and reproducibly lower global FC for the AD group compared to SCD, in the alpha (8–13 Hz) and beta (13–30 Hz) bands, while the PLI revealed reproducibly lower FC for the AD group in the delta (0.5–4 Hz) band and higher FC for the theta (4–8 Hz) band. Regionally, the beta band AEC-c showed reproducibility for almost all ROIs (except for 13 ROIs in the frontal and temporal lobes). For the other bands, the AEC-c and PLI did not show regional reproducibility after FDR correction. The theta band PLI was susceptible to the effect of relative power. CONCLUSION: For MEG, the AEC-c is a sensitive and reproducible metric, able to distinguish FC differences between patients with AD dementia and cognitively healthy controls. These two measures likely reflect different aspects of neural activity and show differential sensitivity to changes in neural dynamics. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13195-022-00970-4. BioMed Central 2022-02-26 /pmc/articles/PMC8881826/ /pubmed/35219327 http://dx.doi.org/10.1186/s13195-022-00970-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Schoonhoven, Deborah N. Briels, Casper T. Hillebrand, Arjan Scheltens, Philip Stam, Cornelis J. Gouw, Alida A. Sensitive and reproducible MEG resting-state metrics of functional connectivity in Alzheimer’s disease |
title | Sensitive and reproducible MEG resting-state metrics of functional connectivity in Alzheimer’s disease |
title_full | Sensitive and reproducible MEG resting-state metrics of functional connectivity in Alzheimer’s disease |
title_fullStr | Sensitive and reproducible MEG resting-state metrics of functional connectivity in Alzheimer’s disease |
title_full_unstemmed | Sensitive and reproducible MEG resting-state metrics of functional connectivity in Alzheimer’s disease |
title_short | Sensitive and reproducible MEG resting-state metrics of functional connectivity in Alzheimer’s disease |
title_sort | sensitive and reproducible meg resting-state metrics of functional connectivity in alzheimer’s disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881826/ https://www.ncbi.nlm.nih.gov/pubmed/35219327 http://dx.doi.org/10.1186/s13195-022-00970-4 |
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