Prosocial behavior relates to the rate and timing of cortical thinning from adolescence to young adulthood.
Adolescence
Cortical thickness
Development
Longitudinal
Prosocial behavior
Structural MRI
Journal
Developmental cognitive neuroscience
ISSN: 1878-9307
Titre abrégé: Dev Cogn Neurosci
Pays: Netherlands
ID NLM: 101541838
Informations de publication
Date de publication:
12 2019
12 2019
Historique:
received:
01
04
2019
revised:
21
10
2019
accepted:
04
11
2019
pubmed:
19
11
2019
medline:
13
3
2020
entrez:
19
11
2019
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 31739096
pii: S1878-9293(19)30321-4
doi: 10.1016/j.dcn.2019.100734
pmc: PMC6974908
pii:
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
100734Subventions
Organisme : NIMH NIH HHS
ID : R01 MH107418
Pays : United States
Informations de copyright
Copyright © 2019. Published by Elsevier Ltd.
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