Cargando…

Standard multiscale entropy reflects neural dynamics at mismatched temporal scales: What’s signal irregularity got to do with it?

Multiscale Entropy (MSE) is used to characterize the temporal irregularity of neural time series patterns. Due to its’ presumed sensitivity to non-linear signal characteristics, MSE is typically considered a complementary measure of brain dynamics to signal variance and spectral power. However, the...

Descripción completa

Detalles Bibliográficos
Autores principales: Kosciessa, Julian Q., Kloosterman, Niels A., Garrett, Douglas D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241858/
https://www.ncbi.nlm.nih.gov/pubmed/32392250
http://dx.doi.org/10.1371/journal.pcbi.1007885
_version_ 1783537145940541440
author Kosciessa, Julian Q.
Kloosterman, Niels A.
Garrett, Douglas D.
author_facet Kosciessa, Julian Q.
Kloosterman, Niels A.
Garrett, Douglas D.
author_sort Kosciessa, Julian Q.
collection PubMed
description Multiscale Entropy (MSE) is used to characterize the temporal irregularity of neural time series patterns. Due to its’ presumed sensitivity to non-linear signal characteristics, MSE is typically considered a complementary measure of brain dynamics to signal variance and spectral power. However, the divergence between these measures is often unclear in application. Furthermore, it is commonly assumed (yet sparingly verified) that entropy estimated at specific time scales reflects signal irregularity at those precise time scales of brain function. We argue that such assumptions are not tenable. Using simulated and empirical electroencephalogram (EEG) data from 47 younger and 52 older adults, we indicate strong and previously underappreciated associations between MSE and spectral power, and highlight how these links preclude traditional interpretations of MSE time scales. Specifically, we show that the typical definition of temporal patterns via “similarity bounds” biases coarse MSE scales–that are thought to reflect slow dynamics–by high-frequency dynamics. Moreover, we demonstrate that entropy at fine time scales–presumed to indicate fast dynamics–is highly sensitive to broadband spectral power, a measure dominated by low-frequency contributions. Jointly, these issues produce counterintuitive reflections of frequency-specific content on MSE time scales. We emphasize the resulting inferential problems in a conceptual replication of cross-sectional age differences at rest, in which scale-specific entropy age effects could be explained by spectral power differences at mismatched temporal scales. Furthermore, we demonstrate how such problems may be alleviated, resulting in the indication of scale-specific age differences in rhythmic irregularity. By controlling for narrowband contributions, we indicate that spontaneous alpha rhythms during eyes open rest transiently reduce broadband signal irregularity. Finally, we recommend best practices that may better permit a valid estimation and interpretation of neural signal irregularity at time scales of interest.
format Online
Article
Text
id pubmed-7241858
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-72418582020-06-03 Standard multiscale entropy reflects neural dynamics at mismatched temporal scales: What’s signal irregularity got to do with it? Kosciessa, Julian Q. Kloosterman, Niels A. Garrett, Douglas D. PLoS Comput Biol Research Article Multiscale Entropy (MSE) is used to characterize the temporal irregularity of neural time series patterns. Due to its’ presumed sensitivity to non-linear signal characteristics, MSE is typically considered a complementary measure of brain dynamics to signal variance and spectral power. However, the divergence between these measures is often unclear in application. Furthermore, it is commonly assumed (yet sparingly verified) that entropy estimated at specific time scales reflects signal irregularity at those precise time scales of brain function. We argue that such assumptions are not tenable. Using simulated and empirical electroencephalogram (EEG) data from 47 younger and 52 older adults, we indicate strong and previously underappreciated associations between MSE and spectral power, and highlight how these links preclude traditional interpretations of MSE time scales. Specifically, we show that the typical definition of temporal patterns via “similarity bounds” biases coarse MSE scales–that are thought to reflect slow dynamics–by high-frequency dynamics. Moreover, we demonstrate that entropy at fine time scales–presumed to indicate fast dynamics–is highly sensitive to broadband spectral power, a measure dominated by low-frequency contributions. Jointly, these issues produce counterintuitive reflections of frequency-specific content on MSE time scales. We emphasize the resulting inferential problems in a conceptual replication of cross-sectional age differences at rest, in which scale-specific entropy age effects could be explained by spectral power differences at mismatched temporal scales. Furthermore, we demonstrate how such problems may be alleviated, resulting in the indication of scale-specific age differences in rhythmic irregularity. By controlling for narrowband contributions, we indicate that spontaneous alpha rhythms during eyes open rest transiently reduce broadband signal irregularity. Finally, we recommend best practices that may better permit a valid estimation and interpretation of neural signal irregularity at time scales of interest. Public Library of Science 2020-05-11 /pmc/articles/PMC7241858/ /pubmed/32392250 http://dx.doi.org/10.1371/journal.pcbi.1007885 Text en © 2020 Kosciessa et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kosciessa, Julian Q.
Kloosterman, Niels A.
Garrett, Douglas D.
Standard multiscale entropy reflects neural dynamics at mismatched temporal scales: What’s signal irregularity got to do with it?
title Standard multiscale entropy reflects neural dynamics at mismatched temporal scales: What’s signal irregularity got to do with it?
title_full Standard multiscale entropy reflects neural dynamics at mismatched temporal scales: What’s signal irregularity got to do with it?
title_fullStr Standard multiscale entropy reflects neural dynamics at mismatched temporal scales: What’s signal irregularity got to do with it?
title_full_unstemmed Standard multiscale entropy reflects neural dynamics at mismatched temporal scales: What’s signal irregularity got to do with it?
title_short Standard multiscale entropy reflects neural dynamics at mismatched temporal scales: What’s signal irregularity got to do with it?
title_sort standard multiscale entropy reflects neural dynamics at mismatched temporal scales: what’s signal irregularity got to do with it?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241858/
https://www.ncbi.nlm.nih.gov/pubmed/32392250
http://dx.doi.org/10.1371/journal.pcbi.1007885
work_keys_str_mv AT kosciessajulianq standardmultiscaleentropyreflectsneuraldynamicsatmismatchedtemporalscaleswhatssignalirregularitygottodowithit
AT kloostermannielsa standardmultiscaleentropyreflectsneuraldynamicsatmismatchedtemporalscaleswhatssignalirregularitygottodowithit
AT garrettdouglasd standardmultiscaleentropyreflectsneuraldynamicsatmismatchedtemporalscaleswhatssignalirregularitygottodowithit