Autism is a devastating and common developmental disorder and a major public health concern. Early detection of autism in high risk infants is critical to these children, their families, and the systems that support them. Fragile X syndrome (FXS) is the leading genetic cause of autism, and both FXS and the FMR1 premutation (FXpm) are highly associated with autism. Despite the high association of autism and FMR1 gene mutations, no study has examined early indicators of autism in FXS or FXpm or examined specificity of early autism indicators in FX to idiopathic (non-FX) autism. This application """"""""Emergence and Stability of Autism in Fragile X Syndrome"""""""" proposes a longitudinal prospective study of the early autism features in infants with FXS and FXpm at 9, 12, and 24 in contrast to infants with an older sibling diagnosed with autism (hereafter referred to as """"""""ASIBS"""""""") and typical controls (TD). This application takes advantage of recent scientific advances in the identification of autism in the first 2 years of life, characterization of the FXS and FXpm-autism co-morbidity and findings from developmental neuroscience to identify underlying physiological mechanisms associated with early emerging autistic features (e.g., attention). This work will advance our understanding of the progression of autism features during the key risk transition period for two conditions of major health importance: FX and autism. In this project, we will use a combined behavioral, both standardized and laboratory measures, and biomarker approach focused on autistic behavior as a continuum rather than rigid diagnostic categories.
Autism is a Devastating and Common Developmental Disorder that is a Major Public Health Concern. With a prevalence of ~1:110 (1:70 males) and a cost of $35 billion per year, the early detection of autism in high risk infants is critical to these children, their families and the systems that support them.
|Roberts, Jane E; McCary, Lindsay M; Shinkareva, Svetlana V et al. (2016) Infant Development in Fragile X Syndrome: Cross-Syndrome Comparisons. J Autism Dev Disord 46:2088-99|
|Roberts, Jane E; Tonnsen, Bridgette L; McCary, Lindsay M et al. (2016) Trajectory and Predictors of Depression and Anxiety Disorders in Mothers With the FMR1 Premutation. Biol Psychiatry 79:850-7|
|Roberts, Jane E; Tonnsen, Bridgette L; McCary, Lindsay M et al. (2016) Brief Report: Autism Symptoms in Infants with Fragile X Syndrome. J Autism Dev Disord 46:3830-3837|
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|Scherr, Jessica F; Hahn, Laura J; Hooper, Stephen R et al. (2016) HPA axis function predicts development of working memory in boys with FXS. Brain Cogn 102:80-90|
|Robinson, Ashley N; Roberts, Jane E; Brady, Nancy C et al. (2016) Physiological Correlates of Maternal Responsivity in Mothers of Preschoolers With Fragile X Syndrome. Am J Intellect Dev Disabil 121:111-20|
|Klusek, Jessica; McGrath, Sara E; Abbeduto, Leonard et al. (2016) Pragmatic Language Features of Mothers With the FMR1 Premutation Are Associated With the Language Outcomes of Adolescents and Young Adults With Fragile X Syndrome. J Speech Lang Hear Res 59:49-61|
|Klusek, Jessica; Roberts, Jane E; Losh, Molly (2015) Cardiac autonomic regulation in autism and Fragile X syndrome: a review. Psychol Bull 141:141-75|
|Kover, Sara T; McCary, Lindsay M; Ingram, Alexandra M et al. (2015) Language development in infants and toddlers with fragile X syndrome: change over time and the role of attention. Am J Intellect Dev Disabil 120:125-44|
|Klusek, Jessica; Hunt, Anna W; Mirrett, Penny L et al. (2015) Reading and phonological skills in boys with fragile X syndrome. J Autism Dev Disord 45:1699-711|
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