4.2 Article

The Association Between Somatic Health, Autism Spectrum Disorder, and Autistic Traits

期刊

BEHAVIOR GENETICS
卷 50, 期 4, 页码 233-246

出版社

SPRINGER
DOI: 10.1007/s10519-019-09986-3

关键词

Autism spectrum disorder; ASD; Neurodevelopmental disorders; Autistic traits; Twins; Comorbidity; Health; Neurology

资金

  1. Karolinska Institute
  2. Swedish Research Council
  3. Vinnova
  4. Formas
  5. FORTE
  6. Swedish Brain foundation (Hjarnfonden)
  7. Stockholm Brain Institute
  8. Autism and Asperger Association Stockholm
  9. Queen Silvia Jubilee Fund
  10. Solstickan Foundation
  11. PRIMA Child and Adult Psychiatry
  12. Pediatric Research Foundation at Astrid Lindgren Children's Hospital
  13. Sallskapet Barnavard
  14. Swedish Foundation for Strategic Research
  15. Jerring Foundation
  16. Swedish Order of Freemasons
  17. Kempe- Carlgrenska Foundation
  18. Sunnderdahls Handikappsfond
  19. Jeansson Foundation
  20. EU-AIMS (European Autism Intervention)
  21. Innovative Medicines Initiative Joint Undertaking [115300]
  22. European Union
  23. new IMI initiative-EU AIMS-2-TRIALS
  24. Autism Speaks

向作者/读者索取更多资源

This study used a twin cohort to investigate the association of autism spectrum disorder (ASD) and autistic traits with somatic health. A total of 344 twins (172 pairs; mean age 15.56 +/- 5.62 years) enriched for ASD and other neurodevelopmental conditions were examined. Medical history and current physical problems were collected with a validated questionnaire to determine twin's somatic health. The Social Responsiveness Scale (SRS-2) was used to measure the participant's severity of autistic traits. Identified somatic health issues with significant within-twin pair differences were tested in relation to both ASD diagnosis and autistic traits in a co-twin control model. Twins with ASD exhibited more neurological and immunological health problems compared to those without ASD (p = 0.005 and p = 0.004, respectively). The intra-pair differences of neurological conditions and SRS-2 score were significantly correlated in monozygotic twins differing for autism traits (r = 0.40, p = 0.001), while the correlation was not found for immunological problems. In addition, a conditional model for analysis of within-twin pair effects revealed an association between neurological problems and clinical ASD diagnosis (Odds ratio per neurological problem 3.15, p = 0.02), as well as autistic traits (beta = 10.44, p = 0.006), after adjusting for possible effects of co-existing attention deficit hyperactivity disorder and general intellectual abilities. Our findings suggest that neurological problems are associated with autism, and that non-shared environmental factors contribute to the overlap for both clinical ASD and autistic traits. Further population-based twin studies are warranted to validate our results and examine in detailed the shared genetic and environmental contributions of neurological problems and ASD.

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