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Early negative affect in males and females with fragile X syndrome: implications for anxiety and autism
BACKGROUND: Fragile X syndrome (FXS) is a genetic disorder that is highly comorbid with anxiety and autism spectrum disorder (ASD). Elevated negative affect in young children has been associated with increased risk for both anxiety and ASD; however, these relations remain poorly understood in FXS. M...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744625/ https://www.ncbi.nlm.nih.gov/pubmed/31519170 http://dx.doi.org/10.1186/s11689-019-9284-y |
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author | Wall, Carla A. Hogan, Abigail L. Will, Elizabeth A. McQuillin, Samuel Kelleher, Bridgette L. Roberts, Jane E. |
author_facet | Wall, Carla A. Hogan, Abigail L. Will, Elizabeth A. McQuillin, Samuel Kelleher, Bridgette L. Roberts, Jane E. |
author_sort | Wall, Carla A. |
collection | PubMed |
description | BACKGROUND: Fragile X syndrome (FXS) is a genetic disorder that is highly comorbid with anxiety and autism spectrum disorder (ASD). Elevated negative affect in young children has been associated with increased risk for both anxiety and ASD; however, these relations remain poorly understood in FXS. METHODS: The present prospective longitudinal study examined the trajectory of negative affect from infancy through preschool in males and females with FXS and typical development and its relation to anxiety and ASD. RESULTS: Results indicate a complex association reflecting group, developmental, and sex effects. Specifically, the group with FXS displayed a trajectory of increasing negative affect across age that was distinct from the typical controls. This atypical trajectory of negative affect in FXS was driven by sex effects in that males showed lower negative affect during infancy followed by steep increases across the toddler and preschool years whereas the females displayed a flatter trajectory. Finally, elevated negative affect predicted anxiety symptoms in males, but not females, with no relationship to ASD in males or females with FXS. CONCLUSIONS: The current work addresses the importance of studying the development of psychopathology in a specific neurogenetic population. Temperamental negative affect was shown to be an important early marker for anxiety in young children with FXS, with subtle differences observed between males and females. |
format | Online Article Text |
id | pubmed-6744625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67446252019-09-18 Early negative affect in males and females with fragile X syndrome: implications for anxiety and autism Wall, Carla A. Hogan, Abigail L. Will, Elizabeth A. McQuillin, Samuel Kelleher, Bridgette L. Roberts, Jane E. J Neurodev Disord Research BACKGROUND: Fragile X syndrome (FXS) is a genetic disorder that is highly comorbid with anxiety and autism spectrum disorder (ASD). Elevated negative affect in young children has been associated with increased risk for both anxiety and ASD; however, these relations remain poorly understood in FXS. METHODS: The present prospective longitudinal study examined the trajectory of negative affect from infancy through preschool in males and females with FXS and typical development and its relation to anxiety and ASD. RESULTS: Results indicate a complex association reflecting group, developmental, and sex effects. Specifically, the group with FXS displayed a trajectory of increasing negative affect across age that was distinct from the typical controls. This atypical trajectory of negative affect in FXS was driven by sex effects in that males showed lower negative affect during infancy followed by steep increases across the toddler and preschool years whereas the females displayed a flatter trajectory. Finally, elevated negative affect predicted anxiety symptoms in males, but not females, with no relationship to ASD in males or females with FXS. CONCLUSIONS: The current work addresses the importance of studying the development of psychopathology in a specific neurogenetic population. Temperamental negative affect was shown to be an important early marker for anxiety in young children with FXS, with subtle differences observed between males and females. BioMed Central 2019-09-13 /pmc/articles/PMC6744625/ /pubmed/31519170 http://dx.doi.org/10.1186/s11689-019-9284-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Wall, Carla A. Hogan, Abigail L. Will, Elizabeth A. McQuillin, Samuel Kelleher, Bridgette L. Roberts, Jane E. Early negative affect in males and females with fragile X syndrome: implications for anxiety and autism |
title | Early negative affect in males and females with fragile X syndrome: implications for anxiety and autism |
title_full | Early negative affect in males and females with fragile X syndrome: implications for anxiety and autism |
title_fullStr | Early negative affect in males and females with fragile X syndrome: implications for anxiety and autism |
title_full_unstemmed | Early negative affect in males and females with fragile X syndrome: implications for anxiety and autism |
title_short | Early negative affect in males and females with fragile X syndrome: implications for anxiety and autism |
title_sort | early negative affect in males and females with fragile x syndrome: implications for anxiety and autism |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744625/ https://www.ncbi.nlm.nih.gov/pubmed/31519170 http://dx.doi.org/10.1186/s11689-019-9284-y |
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