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Prosocial behavior relates to the rate and timing of cortical thinning from adolescence to young adulthood

Prosocial behavior, or voluntary actions that intentionally benefit others, relate to desirable developmental outcomes such as peer acceptance, while lack of prosocial behavior has been associated with several neurodevelopmental disorders. Mapping the biological foundations of prosociality may thus...

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Autores principales: Ferschmann, Lia, Vijayakumar, Nandita, Grydeland, Håkon, Overbye, Knut, Sederevicius, Donatas, Due-Tønnessen, Paulina, Fjell, Anders M., Walhovd, Kristine B., Pfeifer, Jennifer H., Tamnes, Christian K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974908/
https://www.ncbi.nlm.nih.gov/pubmed/31739096
http://dx.doi.org/10.1016/j.dcn.2019.100734
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author Ferschmann, Lia
Vijayakumar, Nandita
Grydeland, Håkon
Overbye, Knut
Sederevicius, Donatas
Due-Tønnessen, Paulina
Fjell, Anders M.
Walhovd, Kristine B.
Pfeifer, Jennifer H.
Tamnes, Christian K.
author_facet Ferschmann, Lia
Vijayakumar, Nandita
Grydeland, Håkon
Overbye, Knut
Sederevicius, Donatas
Due-Tønnessen, Paulina
Fjell, Anders M.
Walhovd, Kristine B.
Pfeifer, Jennifer H.
Tamnes, Christian K.
author_sort Ferschmann, Lia
collection PubMed
description Prosocial behavior, or voluntary actions that intentionally benefit others, relate to desirable developmental outcomes such as peer acceptance, while lack of prosocial behavior has been associated with several neurodevelopmental disorders. Mapping the biological foundations of prosociality may thus aid our understanding of both normal and abnormal development, yet how prosociality relates to cortical development is largely unknown. Here, relations between prosociality, as measured by the Strengths and Difficulties Questionnaire (self-report), and changes in thickness across the cortical mantle were examined using mixed-effects models. The sample consisted of 169 healthy individuals (92 females) aged 12–26 with repeated MRI from up to 3 time points, at approximately 3-year intervals (301 scans). In regions associated with social cognition and behavioral control, higher prosociality was associated with greater cortical thinning during early-to-middle adolescence, followed by attenuation of this process during the transition to young adulthood. Comparatively, lower prosociality was related to initially slower thinning, followed by comparatively protracted thinning into the mid-twenties. This study showed that prosocial behavior is associated with regional development of cortical thickness in adolescence and young adulthood. The results suggest that the rate of thinning in these regions, as well as its timing, may be factors related to prosocial behavior.
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spelling pubmed-69749082020-01-27 Prosocial behavior relates to the rate and timing of cortical thinning from adolescence to young adulthood Ferschmann, Lia Vijayakumar, Nandita Grydeland, Håkon Overbye, Knut Sederevicius, Donatas Due-Tønnessen, Paulina Fjell, Anders M. Walhovd, Kristine B. Pfeifer, Jennifer H. Tamnes, Christian K. Dev Cogn Neurosci Flux 2018: Mechanisms of Learning & Plasticity Prosocial behavior, or voluntary actions that intentionally benefit others, relate to desirable developmental outcomes such as peer acceptance, while lack of prosocial behavior has been associated with several neurodevelopmental disorders. Mapping the biological foundations of prosociality may thus aid our understanding of both normal and abnormal development, yet how prosociality relates to cortical development is largely unknown. Here, relations between prosociality, as measured by the Strengths and Difficulties Questionnaire (self-report), and changes in thickness across the cortical mantle were examined using mixed-effects models. The sample consisted of 169 healthy individuals (92 females) aged 12–26 with repeated MRI from up to 3 time points, at approximately 3-year intervals (301 scans). In regions associated with social cognition and behavioral control, higher prosociality was associated with greater cortical thinning during early-to-middle adolescence, followed by attenuation of this process during the transition to young adulthood. Comparatively, lower prosociality was related to initially slower thinning, followed by comparatively protracted thinning into the mid-twenties. This study showed that prosocial behavior is associated with regional development of cortical thickness in adolescence and young adulthood. The results suggest that the rate of thinning in these regions, as well as its timing, may be factors related to prosocial behavior. Elsevier 2019-11-06 /pmc/articles/PMC6974908/ /pubmed/31739096 http://dx.doi.org/10.1016/j.dcn.2019.100734 Text en © 2019 The Authors. Published by Elsevier Ltd. 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 Flux 2018: Mechanisms of Learning & Plasticity
Ferschmann, Lia
Vijayakumar, Nandita
Grydeland, Håkon
Overbye, Knut
Sederevicius, Donatas
Due-Tønnessen, Paulina
Fjell, Anders M.
Walhovd, Kristine B.
Pfeifer, Jennifer H.
Tamnes, Christian K.
Prosocial behavior relates to the rate and timing of cortical thinning from adolescence to young adulthood
title Prosocial behavior relates to the rate and timing of cortical thinning from adolescence to young adulthood
title_full Prosocial behavior relates to the rate and timing of cortical thinning from adolescence to young adulthood
title_fullStr Prosocial behavior relates to the rate and timing of cortical thinning from adolescence to young adulthood
title_full_unstemmed Prosocial behavior relates to the rate and timing of cortical thinning from adolescence to young adulthood
title_short Prosocial behavior relates to the rate and timing of cortical thinning from adolescence to young adulthood
title_sort prosocial behavior relates to the rate and timing of cortical thinning from adolescence to young adulthood
topic Flux 2018: Mechanisms of Learning & Plasticity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974908/
https://www.ncbi.nlm.nih.gov/pubmed/31739096
http://dx.doi.org/10.1016/j.dcn.2019.100734
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