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Intrinsic brain activity patterns across large‐scale networks predict reciprocity propensity

Reciprocity is prevalent across human societies, but individuals are heterogeneous regarding their reciprocity propensity. Although a large body of task‐based brain imaging measures has shed light on the neural underpinnings of reciprocity at group level, the neural basis underlying the individual d...

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Autores principales: Li, Ting, Pei, Zhaodi, Zhu, Zhiyuan, Wu, Xia, Feng, Chunliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9704792/
https://www.ncbi.nlm.nih.gov/pubmed/36054523
http://dx.doi.org/10.1002/hbm.26038
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author Li, Ting
Pei, Zhaodi
Zhu, Zhiyuan
Wu, Xia
Feng, Chunliang
author_facet Li, Ting
Pei, Zhaodi
Zhu, Zhiyuan
Wu, Xia
Feng, Chunliang
author_sort Li, Ting
collection PubMed
description Reciprocity is prevalent across human societies, but individuals are heterogeneous regarding their reciprocity propensity. Although a large body of task‐based brain imaging measures has shed light on the neural underpinnings of reciprocity at group level, the neural basis underlying the individual differences in reciprocity propensity remains largely unclear. Here, we combined brain imaging and machine learning techniques to individually predict reciprocity propensity from resting‐state brain activity measured by fractional amplitude of low‐frequency fluctuation. The brain regions contributing to the prediction were then analyzed for functional connectivity and decoding analyses, allowing for a data‐driven quantitative inference on psychophysiological functions. Our results indicated that patterns of resting‐state brain activity across multiple brain systems were capable of predicting individual reciprocity propensity, with the contributing regions distributed across the salience (e.g., ventrolateral prefrontal cortex), fronto‐parietal (e.g., dorsolateral prefrontal cortex), default mode (e.g., ventromedial prefrontal cortex), and sensorimotor (e.g., supplementary motor area) networks. Those contributing brain networks are implicated in emotion and cognitive control, mentalizing, and motor‐based processes, respectively. Collectively, these findings provide novel evidence on the neural signatures underlying the individual differences in reciprocity, and lend support the assertion that reciprocity emerges from interactions among regions embodied in multiple large‐scale brain networks.
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spelling pubmed-97047922022-11-29 Intrinsic brain activity patterns across large‐scale networks predict reciprocity propensity Li, Ting Pei, Zhaodi Zhu, Zhiyuan Wu, Xia Feng, Chunliang Hum Brain Mapp Research Articles Reciprocity is prevalent across human societies, but individuals are heterogeneous regarding their reciprocity propensity. Although a large body of task‐based brain imaging measures has shed light on the neural underpinnings of reciprocity at group level, the neural basis underlying the individual differences in reciprocity propensity remains largely unclear. Here, we combined brain imaging and machine learning techniques to individually predict reciprocity propensity from resting‐state brain activity measured by fractional amplitude of low‐frequency fluctuation. The brain regions contributing to the prediction were then analyzed for functional connectivity and decoding analyses, allowing for a data‐driven quantitative inference on psychophysiological functions. Our results indicated that patterns of resting‐state brain activity across multiple brain systems were capable of predicting individual reciprocity propensity, with the contributing regions distributed across the salience (e.g., ventrolateral prefrontal cortex), fronto‐parietal (e.g., dorsolateral prefrontal cortex), default mode (e.g., ventromedial prefrontal cortex), and sensorimotor (e.g., supplementary motor area) networks. Those contributing brain networks are implicated in emotion and cognitive control, mentalizing, and motor‐based processes, respectively. Collectively, these findings provide novel evidence on the neural signatures underlying the individual differences in reciprocity, and lend support the assertion that reciprocity emerges from interactions among regions embodied in multiple large‐scale brain networks. John Wiley & Sons, Inc. 2022-08-22 /pmc/articles/PMC9704792/ /pubmed/36054523 http://dx.doi.org/10.1002/hbm.26038 Text en © 2022 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Li, Ting
Pei, Zhaodi
Zhu, Zhiyuan
Wu, Xia
Feng, Chunliang
Intrinsic brain activity patterns across large‐scale networks predict reciprocity propensity
title Intrinsic brain activity patterns across large‐scale networks predict reciprocity propensity
title_full Intrinsic brain activity patterns across large‐scale networks predict reciprocity propensity
title_fullStr Intrinsic brain activity patterns across large‐scale networks predict reciprocity propensity
title_full_unstemmed Intrinsic brain activity patterns across large‐scale networks predict reciprocity propensity
title_short Intrinsic brain activity patterns across large‐scale networks predict reciprocity propensity
title_sort intrinsic brain activity patterns across large‐scale networks predict reciprocity propensity
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9704792/
https://www.ncbi.nlm.nih.gov/pubmed/36054523
http://dx.doi.org/10.1002/hbm.26038
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