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Point process temporal structure characterizes electrodermal activity
Electrodermal activity (EDA) is a direct readout of the body’s sympathetic nervous system measured as sweat-induced changes in the skin’s electrical conductance. There is growing interest in using EDA to track physiological conditions such as stress levels, sleep quality, and emotional states. Stand...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584910/ https://www.ncbi.nlm.nih.gov/pubmed/33008878 http://dx.doi.org/10.1073/pnas.2004403117 |
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author | Subramanian, Sandya Barbieri, Riccardo Brown, Emery N. |
author_facet | Subramanian, Sandya Barbieri, Riccardo Brown, Emery N. |
author_sort | Subramanian, Sandya |
collection | PubMed |
description | Electrodermal activity (EDA) is a direct readout of the body’s sympathetic nervous system measured as sweat-induced changes in the skin’s electrical conductance. There is growing interest in using EDA to track physiological conditions such as stress levels, sleep quality, and emotional states. Standardized EDA data analysis methods are readily available. However, none considers an established physiological feature of EDA. The sympathetically mediated pulsatile changes in skin sweat measured as EDA resemble an integrate-and-fire process. An integrate-and-fire process modeled as a Gaussian random walk with drift diffusion yields an inverse Gaussian model as the interpulse interval distribution. Therefore, we chose an inverse Gaussian model as our principal probability model to characterize EDA interpulse interval distributions. To analyze deviations from the inverse Gaussian model, we considered a broader model set: the generalized inverse Gaussian distribution, which includes the inverse Gaussian and other diffusion and nondiffusion models; the lognormal distribution which has heavier tails (lower settling rates) than the inverse Gaussian; and the gamma and exponential probability distributions which have lighter tails (higher settling rates) than the inverse Gaussian. To assess the validity of these probability models we recorded and analyzed EDA measurements in 11 healthy volunteers during 1 h of quiet wakefulness. Each of the 11 time series was accurately described by an inverse Gaussian model measured by Kolmogorov–Smirnov measures. Our broader model set offered a useful framework to enhance further statistical descriptions of EDA. Our findings establish that a physiologically based inverse Gaussian probability model provides a parsimonious and accurate description of EDA. |
format | Online Article Text |
id | pubmed-7584910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-75849102020-10-30 Point process temporal structure characterizes electrodermal activity Subramanian, Sandya Barbieri, Riccardo Brown, Emery N. Proc Natl Acad Sci U S A Biological Sciences Electrodermal activity (EDA) is a direct readout of the body’s sympathetic nervous system measured as sweat-induced changes in the skin’s electrical conductance. There is growing interest in using EDA to track physiological conditions such as stress levels, sleep quality, and emotional states. Standardized EDA data analysis methods are readily available. However, none considers an established physiological feature of EDA. The sympathetically mediated pulsatile changes in skin sweat measured as EDA resemble an integrate-and-fire process. An integrate-and-fire process modeled as a Gaussian random walk with drift diffusion yields an inverse Gaussian model as the interpulse interval distribution. Therefore, we chose an inverse Gaussian model as our principal probability model to characterize EDA interpulse interval distributions. To analyze deviations from the inverse Gaussian model, we considered a broader model set: the generalized inverse Gaussian distribution, which includes the inverse Gaussian and other diffusion and nondiffusion models; the lognormal distribution which has heavier tails (lower settling rates) than the inverse Gaussian; and the gamma and exponential probability distributions which have lighter tails (higher settling rates) than the inverse Gaussian. To assess the validity of these probability models we recorded and analyzed EDA measurements in 11 healthy volunteers during 1 h of quiet wakefulness. Each of the 11 time series was accurately described by an inverse Gaussian model measured by Kolmogorov–Smirnov measures. Our broader model set offered a useful framework to enhance further statistical descriptions of EDA. Our findings establish that a physiologically based inverse Gaussian probability model provides a parsimonious and accurate description of EDA. National Academy of Sciences 2020-10-20 2020-10-02 /pmc/articles/PMC7584910/ /pubmed/33008878 http://dx.doi.org/10.1073/pnas.2004403117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Subramanian, Sandya Barbieri, Riccardo Brown, Emery N. Point process temporal structure characterizes electrodermal activity |
title | Point process temporal structure characterizes electrodermal activity |
title_full | Point process temporal structure characterizes electrodermal activity |
title_fullStr | Point process temporal structure characterizes electrodermal activity |
title_full_unstemmed | Point process temporal structure characterizes electrodermal activity |
title_short | Point process temporal structure characterizes electrodermal activity |
title_sort | point process temporal structure characterizes electrodermal activity |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584910/ https://www.ncbi.nlm.nih.gov/pubmed/33008878 http://dx.doi.org/10.1073/pnas.2004403117 |
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