Autistic behavior in boys with fragile X syndrome: Social approach and HPA-axis dysfunction

Jane E. Roberts, Megan A. Clarke, Kaitlyn Alcorn, John C. Carter, Anna C J Long, Walter E. Kaufmann

    Research output: Contribution to journalArticle


    The primary goal of this study was to examine environmental and neuroendocrine factors that convey increased risk for elevated autistic behavior in boys with Fragile X syndrome (FXS). This study involves three related analyses: (1) examination of multiple dimensions of social approach behaviors and how they vary over time, (2) investigation of mean levels and modulation of salivary cortisol levels in response to social interaction, and (3) examination of the relationship of social approach and autistic behaviors to salivary cortisol. Poor social approach and elevated baseline and regulation cortisol are discernible traits that distinguish boys with FXS and ASD from boys with FXS only and from typically developing boys. In addition, blunted cortisol change is associated with increased severity of autistic behaviors only within the FXS and ASD group. Boys with FXS and ASD have distinct behavioral and neuroendocrine profiles that differentiate them from those with FXS alone and typically developing boys.

    Original languageEnglish (US)
    Pages (from-to)283-291
    Number of pages9
    JournalJournal of Neurodevelopmental Disorders
    Issue number4
    Publication statusPublished - 2009



    • Autism
    • Cortisol
    • Fragile X
    • Social anxiety
    • Social approach

    ASJC Scopus subject areas

    • Clinical Neurology
    • Pathology and Forensic Medicine
    • Cognitive Neuroscience
    • Pediatrics, Perinatology, and Child Health

    Cite this

    Roberts, J. E., Clarke, M. A., Alcorn, K., Carter, J. C., Long, A. C. J., & Kaufmann, W. E. (2009). Autistic behavior in boys with fragile X syndrome: Social approach and HPA-axis dysfunction. Journal of Neurodevelopmental Disorders, 1(4), 283-291.