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Spatial migration of human reward processing with functional development: Evidence from quantitative meta‐analyses

Functional magnetic resonance imaging (fMRI) studies have shown notable age‐dependent differences in reward processing. We analyzed data from a total of 554 children, 1,059 adolescents, and 1,831 adults from 70 articles. Quantitative meta‐analyses results show that adults engage an extended set of r...

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Detalles Bibliográficos
Autores principales: Yaple, Zachary A, Yu, Rongjun, Arsalidou, Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469823/
https://www.ncbi.nlm.nih.gov/pubmed/32638450
http://dx.doi.org/10.1002/hbm.25103
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author Yaple, Zachary A
Yu, Rongjun
Arsalidou, Marie
author_facet Yaple, Zachary A
Yu, Rongjun
Arsalidou, Marie
author_sort Yaple, Zachary A
collection PubMed
description Functional magnetic resonance imaging (fMRI) studies have shown notable age‐dependent differences in reward processing. We analyzed data from a total of 554 children, 1,059 adolescents, and 1,831 adults from 70 articles. Quantitative meta‐analyses results show that adults engage an extended set of regions that include anterior and posterior cingulate gyri, insula, basal ganglia, and thalamus. Adolescents engage the posterior cingulate and middle frontal gyri as well as the insula and amygdala, whereas children show concordance in right insula and striatal regions almost exclusively. Our data support the notion of reorganization of function over childhood and adolescence and may inform current hypotheses relating to decision‐making across age.
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spelling pubmed-74698232020-09-09 Spatial migration of human reward processing with functional development: Evidence from quantitative meta‐analyses Yaple, Zachary A Yu, Rongjun Arsalidou, Marie Hum Brain Mapp Research Articles Functional magnetic resonance imaging (fMRI) studies have shown notable age‐dependent differences in reward processing. We analyzed data from a total of 554 children, 1,059 adolescents, and 1,831 adults from 70 articles. Quantitative meta‐analyses results show that adults engage an extended set of regions that include anterior and posterior cingulate gyri, insula, basal ganglia, and thalamus. Adolescents engage the posterior cingulate and middle frontal gyri as well as the insula and amygdala, whereas children show concordance in right insula and striatal regions almost exclusively. Our data support the notion of reorganization of function over childhood and adolescence and may inform current hypotheses relating to decision‐making across age. John Wiley & Sons, Inc. 2020-07-07 /pmc/articles/PMC7469823/ /pubmed/32638450 http://dx.doi.org/10.1002/hbm.25103 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Yaple, Zachary A
Yu, Rongjun
Arsalidou, Marie
Spatial migration of human reward processing with functional development: Evidence from quantitative meta‐analyses
title Spatial migration of human reward processing with functional development: Evidence from quantitative meta‐analyses
title_full Spatial migration of human reward processing with functional development: Evidence from quantitative meta‐analyses
title_fullStr Spatial migration of human reward processing with functional development: Evidence from quantitative meta‐analyses
title_full_unstemmed Spatial migration of human reward processing with functional development: Evidence from quantitative meta‐analyses
title_short Spatial migration of human reward processing with functional development: Evidence from quantitative meta‐analyses
title_sort spatial migration of human reward processing with functional development: evidence from quantitative meta‐analyses
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7469823/
https://www.ncbi.nlm.nih.gov/pubmed/32638450
http://dx.doi.org/10.1002/hbm.25103
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