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Multimodal Brain Signal Complexity Predicts Human Intelligence

Spontaneous brain activity builds the foundation for human cognitive processing during external demands. Neuroimaging studies based on functional magnetic resonance imaging (fMRI) identified specific characteristics of spontaneous (intrinsic) brain dynamics to be associated with individual differenc...

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Autores principales: Thiele, Jonas A., Richter, Aylin, Hilger, Kirsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910576/
https://www.ncbi.nlm.nih.gov/pubmed/36657966
http://dx.doi.org/10.1523/ENEURO.0345-22.2022
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author Thiele, Jonas A.
Richter, Aylin
Hilger, Kirsten
author_facet Thiele, Jonas A.
Richter, Aylin
Hilger, Kirsten
author_sort Thiele, Jonas A.
collection PubMed
description Spontaneous brain activity builds the foundation for human cognitive processing during external demands. Neuroimaging studies based on functional magnetic resonance imaging (fMRI) identified specific characteristics of spontaneous (intrinsic) brain dynamics to be associated with individual differences in general cognitive ability, i.e., intelligence. However, fMRI research is inherently limited by low temporal resolution, thus, preventing conclusions about neural fluctuations within the range of milliseconds. Here, we used resting-state electroencephalographical (EEG) recordings from 144 healthy adults to test whether individual differences in intelligence (Raven’s Advanced Progressive Matrices scores) can be predicted from the complexity of temporally highly resolved intrinsic brain signals. We compared different operationalizations of brain signal complexity (multiscale entropy, Shannon entropy, Fuzzy entropy, and specific characteristics of microstates) regarding their relation to intelligence. The results indicate that associations between brain signal complexity measures and intelligence are of small effect sizes (r ∼ 0.20) and vary across different spatial and temporal scales. Specifically, higher intelligence scores were associated with lower complexity in local aspects of neural processing, and less activity in task-negative brain regions belonging to the default-mode network. Finally, we combined multiple measures of brain signal complexity to show that individual intelligence scores can be significantly predicted with a multimodal model within the sample (10-fold cross-validation) as well as in an independent sample (external replication, N = 57). In sum, our results highlight the temporal and spatial dependency of associations between intelligence and intrinsic brain dynamics, proposing multimodal approaches as promising means for future neuroscientific research on complex human traits.
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spelling pubmed-99105762023-02-10 Multimodal Brain Signal Complexity Predicts Human Intelligence Thiele, Jonas A. Richter, Aylin Hilger, Kirsten eNeuro Research Article: New Research Spontaneous brain activity builds the foundation for human cognitive processing during external demands. Neuroimaging studies based on functional magnetic resonance imaging (fMRI) identified specific characteristics of spontaneous (intrinsic) brain dynamics to be associated with individual differences in general cognitive ability, i.e., intelligence. However, fMRI research is inherently limited by low temporal resolution, thus, preventing conclusions about neural fluctuations within the range of milliseconds. Here, we used resting-state electroencephalographical (EEG) recordings from 144 healthy adults to test whether individual differences in intelligence (Raven’s Advanced Progressive Matrices scores) can be predicted from the complexity of temporally highly resolved intrinsic brain signals. We compared different operationalizations of brain signal complexity (multiscale entropy, Shannon entropy, Fuzzy entropy, and specific characteristics of microstates) regarding their relation to intelligence. The results indicate that associations between brain signal complexity measures and intelligence are of small effect sizes (r ∼ 0.20) and vary across different spatial and temporal scales. Specifically, higher intelligence scores were associated with lower complexity in local aspects of neural processing, and less activity in task-negative brain regions belonging to the default-mode network. Finally, we combined multiple measures of brain signal complexity to show that individual intelligence scores can be significantly predicted with a multimodal model within the sample (10-fold cross-validation) as well as in an independent sample (external replication, N = 57). In sum, our results highlight the temporal and spatial dependency of associations between intelligence and intrinsic brain dynamics, proposing multimodal approaches as promising means for future neuroscientific research on complex human traits. Society for Neuroscience 2023-02-02 /pmc/articles/PMC9910576/ /pubmed/36657966 http://dx.doi.org/10.1523/ENEURO.0345-22.2022 Text en Copyright © 2023 Thiele et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article: New Research
Thiele, Jonas A.
Richter, Aylin
Hilger, Kirsten
Multimodal Brain Signal Complexity Predicts Human Intelligence
title Multimodal Brain Signal Complexity Predicts Human Intelligence
title_full Multimodal Brain Signal Complexity Predicts Human Intelligence
title_fullStr Multimodal Brain Signal Complexity Predicts Human Intelligence
title_full_unstemmed Multimodal Brain Signal Complexity Predicts Human Intelligence
title_short Multimodal Brain Signal Complexity Predicts Human Intelligence
title_sort multimodal brain signal complexity predicts human intelligence
topic Research Article: New Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910576/
https://www.ncbi.nlm.nih.gov/pubmed/36657966
http://dx.doi.org/10.1523/ENEURO.0345-22.2022
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