4.7 Article

Recurrence Risk for Autism Spectrum Disorders: A Baby Siblings Research Consortium Study

期刊

PEDIATRICS
卷 128, 期 3, 页码 E488-E495

出版社

AMER ACAD PEDIATRICS
DOI: 10.1542/peds.2010-2825

关键词

autism; recurrence; sibling risk

资金

  1. National Institutes of Health (NIH) [R01 MH068398, R01 DC10290, R01 HD047417, R01HD057284, R01 HD042541, R01 HD052804-01, R01 HD54979, U54 MH066417, R01 MH059630, U54 MH068172, R01 HD043292]
  2. United States-Israel Binational Science Foundation [94-66/3, 97-00073]
  3. Canadian Institute for Health Research [62924, 102665]
  4. Autism Speaks

向作者/读者索取更多资源

OBJECTIVE: The recurrence risk of autism spectrum disorders (ASD) is estimated to be between 3% and 10%, but previous research was limited by small sample sizes and biases related to ascertainment, reporting, and stoppage factors. This study used prospective methods to obtain an updated estimate of sibling recurrence risk for ASD. METHODS: A prospective longitudinal study of infants at risk for ASD was conducted by a multisite international network, the Baby Siblings Research Consortium. Infants (n = 664) with an older biological sibling with ASD were followed from early in life to 36 months, when they were classified as having or not having ASD. An ASD classification required surpassing the cutoff of the Autism Diagnostic Observation Schedule and receiving a clinical diagnosis from an expert clinician. RESULTS: A total of 18.7% of the infants developed ASD. Infant gender and the presence of >1 older affected sibling were significant predictors of ASD outcome, and there was an almost threefold increase in risk for male subjects and an additional twofold increase in risk if there was >1 older affected sibling. The age of the infant at study enrollment, the gender and functioning level of the infant's older sibling, and other demographic factors did not predict ASD outcome. CONCLUSIONS: The sibling recurrence rate of ASD is higher than suggested by previous estimates. The size of the current sample and prospective nature of data collection minimized many limitations of previous studies of sibling recurrence. Clinical implications, including genetic counseling, are discussed. Pediatrics 2011; 128: e488-e495

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