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No transfer of arousal from other’s eyes in Williams syndrome

Typically developing humans automatically synchronize their arousal levels, resulting in pupillary contagion, or spontaneous adaptation of pupil size to that of others. This phenomenon emerges in infancy and is believed to facilitate social interaction. Williams syndrome (WS) is a genetic condition...

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Autores principales: Kleberg, Johan Lundin, Hallman, Astrid E. Z., Galazka, Martyna A., Riby, Deborah M., Bölte, Sven, Willfors, Charlotte, Fawcett, Christine, Nordgren, Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603144/
https://www.ncbi.nlm.nih.gov/pubmed/37884631
http://dx.doi.org/10.1038/s41598-023-45521-5
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author Kleberg, Johan Lundin
Hallman, Astrid E. Z.
Galazka, Martyna A.
Riby, Deborah M.
Bölte, Sven
Willfors, Charlotte
Fawcett, Christine
Nordgren, Ann
author_facet Kleberg, Johan Lundin
Hallman, Astrid E. Z.
Galazka, Martyna A.
Riby, Deborah M.
Bölte, Sven
Willfors, Charlotte
Fawcett, Christine
Nordgren, Ann
author_sort Kleberg, Johan Lundin
collection PubMed
description Typically developing humans automatically synchronize their arousal levels, resulting in pupillary contagion, or spontaneous adaptation of pupil size to that of others. This phenomenon emerges in infancy and is believed to facilitate social interaction. Williams syndrome (WS) is a genetic condition characterized by a hyper-social personality and social interaction challenges. Pupillary contagion was examined in individuals with WS (n = 44), age-parallel-matched typically developing children and adults (n = 65), and infants (n = 79). Bayesian statistics were used. As a group, people with WS did not show pupillary contagion (Bayes factors supporting the null: 25–50) whereas control groups did. This suggests a very early emerging atypical developmental trajectory. In WS, higher pupillary contagion was associated with lower autistic symptoms of social communication. Diminished synchronization of arousal may explain why individuals with WS have social challenges, whereas synchronization of arousal is not a necessary correlate of high social motivation.
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spelling pubmed-106031442023-10-28 No transfer of arousal from other’s eyes in Williams syndrome Kleberg, Johan Lundin Hallman, Astrid E. Z. Galazka, Martyna A. Riby, Deborah M. Bölte, Sven Willfors, Charlotte Fawcett, Christine Nordgren, Ann Sci Rep Article Typically developing humans automatically synchronize their arousal levels, resulting in pupillary contagion, or spontaneous adaptation of pupil size to that of others. This phenomenon emerges in infancy and is believed to facilitate social interaction. Williams syndrome (WS) is a genetic condition characterized by a hyper-social personality and social interaction challenges. Pupillary contagion was examined in individuals with WS (n = 44), age-parallel-matched typically developing children and adults (n = 65), and infants (n = 79). Bayesian statistics were used. As a group, people with WS did not show pupillary contagion (Bayes factors supporting the null: 25–50) whereas control groups did. This suggests a very early emerging atypical developmental trajectory. In WS, higher pupillary contagion was associated with lower autistic symptoms of social communication. Diminished synchronization of arousal may explain why individuals with WS have social challenges, whereas synchronization of arousal is not a necessary correlate of high social motivation. Nature Publishing Group UK 2023-10-26 /pmc/articles/PMC10603144/ /pubmed/37884631 http://dx.doi.org/10.1038/s41598-023-45521-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kleberg, Johan Lundin
Hallman, Astrid E. Z.
Galazka, Martyna A.
Riby, Deborah M.
Bölte, Sven
Willfors, Charlotte
Fawcett, Christine
Nordgren, Ann
No transfer of arousal from other’s eyes in Williams syndrome
title No transfer of arousal from other’s eyes in Williams syndrome
title_full No transfer of arousal from other’s eyes in Williams syndrome
title_fullStr No transfer of arousal from other’s eyes in Williams syndrome
title_full_unstemmed No transfer of arousal from other’s eyes in Williams syndrome
title_short No transfer of arousal from other’s eyes in Williams syndrome
title_sort no transfer of arousal from other’s eyes in williams syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603144/
https://www.ncbi.nlm.nih.gov/pubmed/37884631
http://dx.doi.org/10.1038/s41598-023-45521-5
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