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No association of cortical amyloid load and EEG connectivity in older people with subjective memory complaints

Changes in functional connectivity of cortical networks have been observed in resting-state EEG studies in healthy aging as well as preclinical and clinical stages of AD. Little information, however, exists on associations between EEG connectivity and cortical amyloid load in people with subjective...

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Autores principales: Teipel, Stefan, Bakardjian, Hovagim, Gonzalez-Escamilla, Gabriel, Cavedo, Enrica, Weschke, Sarah, Dyrba, Martin, Grothe, Michel J., Potier, Marie-Claude, Habert, Marie-Odile, Dubois, Bruno, Hampel, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684495/
https://www.ncbi.nlm.nih.gov/pubmed/29159056
http://dx.doi.org/10.1016/j.nicl.2017.10.031
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author Teipel, Stefan
Bakardjian, Hovagim
Gonzalez-Escamilla, Gabriel
Cavedo, Enrica
Weschke, Sarah
Dyrba, Martin
Grothe, Michel J.
Potier, Marie-Claude
Habert, Marie-Odile
Dubois, Bruno
Hampel, Harald
author_facet Teipel, Stefan
Bakardjian, Hovagim
Gonzalez-Escamilla, Gabriel
Cavedo, Enrica
Weschke, Sarah
Dyrba, Martin
Grothe, Michel J.
Potier, Marie-Claude
Habert, Marie-Odile
Dubois, Bruno
Hampel, Harald
author_sort Teipel, Stefan
collection PubMed
description Changes in functional connectivity of cortical networks have been observed in resting-state EEG studies in healthy aging as well as preclinical and clinical stages of AD. Little information, however, exists on associations between EEG connectivity and cortical amyloid load in people with subjective memory complaints. Here, we determined the association of global cortical amyloid load, as measured by florbetapir-PET, with functional connectivity based on the phase-lag index of resting state EEG data for alpha and beta frequency bands in 318 cognitively normal individuals aged 70–85 years with subjective memory complaints from the INSIGHT-preAD cohort. Within the entire group we did not find any significant associations between global amyloid load and phase-lag index in any frequency band. Assessing exclusively the subgroup of amyloid-positive participants, we found enhancement of functional connectivity with higher global amyloid load in the alpha and a reduction in the beta frequency bands. In the amyloid-negative participants, higher amyloid load was associated with lower connectivity in the low alpha band. However, these correlations failed to reach significance after controlling for multiple comparisons. The absence of a strong amyloid effect on functional connectivity may represent a selection effect, where individuals remain in the cognitively normal group only if amyloid accumulation does not impair cortical functional connectivity.
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spelling pubmed-56844952017-11-20 No association of cortical amyloid load and EEG connectivity in older people with subjective memory complaints Teipel, Stefan Bakardjian, Hovagim Gonzalez-Escamilla, Gabriel Cavedo, Enrica Weschke, Sarah Dyrba, Martin Grothe, Michel J. Potier, Marie-Claude Habert, Marie-Odile Dubois, Bruno Hampel, Harald Neuroimage Clin Regular Article Changes in functional connectivity of cortical networks have been observed in resting-state EEG studies in healthy aging as well as preclinical and clinical stages of AD. Little information, however, exists on associations between EEG connectivity and cortical amyloid load in people with subjective memory complaints. Here, we determined the association of global cortical amyloid load, as measured by florbetapir-PET, with functional connectivity based on the phase-lag index of resting state EEG data for alpha and beta frequency bands in 318 cognitively normal individuals aged 70–85 years with subjective memory complaints from the INSIGHT-preAD cohort. Within the entire group we did not find any significant associations between global amyloid load and phase-lag index in any frequency band. Assessing exclusively the subgroup of amyloid-positive participants, we found enhancement of functional connectivity with higher global amyloid load in the alpha and a reduction in the beta frequency bands. In the amyloid-negative participants, higher amyloid load was associated with lower connectivity in the low alpha band. However, these correlations failed to reach significance after controlling for multiple comparisons. The absence of a strong amyloid effect on functional connectivity may represent a selection effect, where individuals remain in the cognitively normal group only if amyloid accumulation does not impair cortical functional connectivity. Elsevier 2017-10-29 /pmc/articles/PMC5684495/ /pubmed/29159056 http://dx.doi.org/10.1016/j.nicl.2017.10.031 Text en © 2017 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Teipel, Stefan
Bakardjian, Hovagim
Gonzalez-Escamilla, Gabriel
Cavedo, Enrica
Weschke, Sarah
Dyrba, Martin
Grothe, Michel J.
Potier, Marie-Claude
Habert, Marie-Odile
Dubois, Bruno
Hampel, Harald
No association of cortical amyloid load and EEG connectivity in older people with subjective memory complaints
title No association of cortical amyloid load and EEG connectivity in older people with subjective memory complaints
title_full No association of cortical amyloid load and EEG connectivity in older people with subjective memory complaints
title_fullStr No association of cortical amyloid load and EEG connectivity in older people with subjective memory complaints
title_full_unstemmed No association of cortical amyloid load and EEG connectivity in older people with subjective memory complaints
title_short No association of cortical amyloid load and EEG connectivity in older people with subjective memory complaints
title_sort no association of cortical amyloid load and eeg connectivity in older people with subjective memory complaints
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684495/
https://www.ncbi.nlm.nih.gov/pubmed/29159056
http://dx.doi.org/10.1016/j.nicl.2017.10.031
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