Cargando…

Neural responsivity to social rewards in autistic female youth

Autism is hypothesized to be in part driven by a reduced sensitivity to the inherently rewarding nature of social stimuli. Previous neuroimaging studies have indicated that autistic males do indeed display reduced neural activity to social rewards, but it is unknown whether this finding extends to a...

Descripción completa

Detalles Bibliográficos
Autores principales: Lawrence, Katherine E., Hernandez, Leanna M., Eilbott, Jeffrey, Jack, Allison, Aylward, Elizabeth, Gaab, Nadine, Van Horn, John D., Bernier, Raphael A., Geschwind, Daniel H., McPartland, James C., Nelson, Charles A., Webb, Sara J., Pelphrey, Kevin A., Bookheimer, Susan Y., Dapretto, Mirella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7266816/
https://www.ncbi.nlm.nih.gov/pubmed/32488083
http://dx.doi.org/10.1038/s41398-020-0824-8
_version_ 1783541377969160192
author Lawrence, Katherine E.
Hernandez, Leanna M.
Eilbott, Jeffrey
Jack, Allison
Aylward, Elizabeth
Gaab, Nadine
Van Horn, John D.
Bernier, Raphael A.
Geschwind, Daniel H.
McPartland, James C.
Nelson, Charles A.
Webb, Sara J.
Pelphrey, Kevin A.
Bookheimer, Susan Y.
Dapretto, Mirella
author_facet Lawrence, Katherine E.
Hernandez, Leanna M.
Eilbott, Jeffrey
Jack, Allison
Aylward, Elizabeth
Gaab, Nadine
Van Horn, John D.
Bernier, Raphael A.
Geschwind, Daniel H.
McPartland, James C.
Nelson, Charles A.
Webb, Sara J.
Pelphrey, Kevin A.
Bookheimer, Susan Y.
Dapretto, Mirella
author_sort Lawrence, Katherine E.
collection PubMed
description Autism is hypothesized to be in part driven by a reduced sensitivity to the inherently rewarding nature of social stimuli. Previous neuroimaging studies have indicated that autistic males do indeed display reduced neural activity to social rewards, but it is unknown whether this finding extends to autistic females, particularly as behavioral evidence suggests that affected females may not exhibit the same reduction in social motivation as their male peers. We therefore used functional magnetic resonance imaging to examine social reward processing during an instrumental implicit learning task in 154 children and adolescents (ages 8–17): 39 autistic girls, 43 autistic boys, 33 typically developing girls, and 39 typically developing boys. We found that autistic girls displayed increased activity to socially rewarding stimuli, including greater activity in the nucleus accumbens relative to autistic boys, as well as greater activity in lateral frontal cortices and the anterior insula compared with typically developing girls. These results demonstrate for the first time that autistic girls do not exhibit the same reduction in activity within social reward systems as autistic boys. Instead, autistic girls display increased neural activation to such stimuli in areas related to reward processing and salience detection. Our findings indicate that a reduced sensitivity to social rewards, as assessed with a rewarded instrumental implicit learning task, does not generalize to affected female youth and highlight the importance of studying potential sex differences in autism to improve our understanding of the condition and its heterogeneity.
format Online
Article
Text
id pubmed-7266816
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-72668162020-06-16 Neural responsivity to social rewards in autistic female youth Lawrence, Katherine E. Hernandez, Leanna M. Eilbott, Jeffrey Jack, Allison Aylward, Elizabeth Gaab, Nadine Van Horn, John D. Bernier, Raphael A. Geschwind, Daniel H. McPartland, James C. Nelson, Charles A. Webb, Sara J. Pelphrey, Kevin A. Bookheimer, Susan Y. Dapretto, Mirella Transl Psychiatry Article Autism is hypothesized to be in part driven by a reduced sensitivity to the inherently rewarding nature of social stimuli. Previous neuroimaging studies have indicated that autistic males do indeed display reduced neural activity to social rewards, but it is unknown whether this finding extends to autistic females, particularly as behavioral evidence suggests that affected females may not exhibit the same reduction in social motivation as their male peers. We therefore used functional magnetic resonance imaging to examine social reward processing during an instrumental implicit learning task in 154 children and adolescents (ages 8–17): 39 autistic girls, 43 autistic boys, 33 typically developing girls, and 39 typically developing boys. We found that autistic girls displayed increased activity to socially rewarding stimuli, including greater activity in the nucleus accumbens relative to autistic boys, as well as greater activity in lateral frontal cortices and the anterior insula compared with typically developing girls. These results demonstrate for the first time that autistic girls do not exhibit the same reduction in activity within social reward systems as autistic boys. Instead, autistic girls display increased neural activation to such stimuli in areas related to reward processing and salience detection. Our findings indicate that a reduced sensitivity to social rewards, as assessed with a rewarded instrumental implicit learning task, does not generalize to affected female youth and highlight the importance of studying potential sex differences in autism to improve our understanding of the condition and its heterogeneity. Nature Publishing Group UK 2020-06-02 /pmc/articles/PMC7266816/ /pubmed/32488083 http://dx.doi.org/10.1038/s41398-020-0824-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lawrence, Katherine E.
Hernandez, Leanna M.
Eilbott, Jeffrey
Jack, Allison
Aylward, Elizabeth
Gaab, Nadine
Van Horn, John D.
Bernier, Raphael A.
Geschwind, Daniel H.
McPartland, James C.
Nelson, Charles A.
Webb, Sara J.
Pelphrey, Kevin A.
Bookheimer, Susan Y.
Dapretto, Mirella
Neural responsivity to social rewards in autistic female youth
title Neural responsivity to social rewards in autistic female youth
title_full Neural responsivity to social rewards in autistic female youth
title_fullStr Neural responsivity to social rewards in autistic female youth
title_full_unstemmed Neural responsivity to social rewards in autistic female youth
title_short Neural responsivity to social rewards in autistic female youth
title_sort neural responsivity to social rewards in autistic female youth
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7266816/
https://www.ncbi.nlm.nih.gov/pubmed/32488083
http://dx.doi.org/10.1038/s41398-020-0824-8
work_keys_str_mv AT lawrencekatherinee neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT hernandezleannam neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT eilbottjeffrey neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT jackallison neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT aylwardelizabeth neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT gaabnadine neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT vanhornjohnd neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT bernierraphaela neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT geschwinddanielh neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT mcpartlandjamesc neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT nelsoncharlesa neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT webbsaraj neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT pelphreykevina neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT bookheimersusany neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT daprettomirella neuralresponsivitytosocialrewardsinautisticfemaleyouth
AT neuralresponsivitytosocialrewardsinautisticfemaleyouth