4.5 Article

Autism Spectrum Symptoms in a Tourette's Disorder Sample

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jaac.2017.05.002

Keywords

Tourette's disorder; autism; obsessive-compulsive disorder; attention-deficit/hyperactivity disorder; heritability

Funding

  1. NIH
  2. International OCD-(Obsessive-Compulsive Disorder) Foundation (IOCDF)
  3. Tourette Association of America (TAA)
  4. Purdue
  5. National Institute of Mental Health [R25 MH060482]
  6. Neurocrine Pharmaceuticals
  7. Psyadon Pharmaceuticals
  8. Otsuka Pharmaceuticals
  9. Synchroneuron Pharmaceuticals
  10. Teva Pharmaceuticals
  11. Auspex Pharmaceuticals
  12. ZONMW
  13. Fonds Psychische Gezondheid
  14. Hersenstichting
  15. Fonds Nuts Ohra
  16. Tourette Syndrome Association USA
  17. Marie Curie Initial Training Networks (ITN)
  18. TAA
  19. TLC Foundation for BFRBs
  20. Nuvelution
  21. Pharma
  22. Abide Pharmaceuticals
  23. Scientific Advisory Board of the Tourette Association of America (TAA)
  24. IOCDF

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Objective: Tourette's disorder (TD) and autism spectrum disorder (ASD) share clinical features and possibly an overlapping etiology. The aims of this study were to examine ASD symptom rates in participants with TD, and to characterize the relationships between ASD symptom patterns and TD, obsessive-compulsive disorder (OCD), and attention-deficit/hyperactivity disorder (ADHD). Method: Participants with TD (n = 535) and their family members (n =234) recruited for genetic studies reported TD, OCD, and ADHD symptoms and completed the Social Responsiveness Scale Second Edition (SRS), which was used to characterize ASD symptoms. Results: SRS scores in participants with TD were similar to those observed in other clinical samples but lower than in ASD samples (mean SRS total raw score = 51; SD = 32.4). More children with TD met cut-off criteria for ASD (22.8%) than adults with TD (8.7%). The elevated rate in children was primarily due to high scores on the SRS Repetitive and Restricted Behaviors (RRB) subscale. Total SRS scores were correlated with TD) (r = 0.27), OCD (r = 0.37), and ADHD (r = 0.44) and were higher among individuals with OCD symptom-based phenotypes than for those with tics alone. Conclusion: Higher observed rates of ASD among children affected by ID may in part be due to difficulty in discriminating complex tics and OCD symptoms from ASD symptoms. Careful examination of ASD-specific symptom patterns (social communication vs. repetitive behaviors) is essential. Independent of ASD, the SRS may be a useful tool for identifying patients with TD with impairments in social communication that potentially place them at risk for bullying and other negative sequelae.

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