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Autism following a history of newborn encephalopathy: more than a coincidence?
Nadia Badawi1, Glenys Dixon, Janine F Felix
1Department of Neonatology, The Children's Hospital at Westmead, University of Sydney, Australia.
Insights
Newborn infants with encephalopathy (NE) face a significantly higher risk of developing autism spectrum disorders (ASDs) by age five. This population-based study highlights a crucial link between birth complications and neurodevelopmental outcomes.
Area of Science:
- Neuroscience
- Developmental Pediatrics
- Public Health
Background:
- Term newborn infants experiencing encephalopathy (NE) may have long-term neurodevelopmental consequences.
- Autism spectrum disorders (ASDs) are complex neurodevelopmental conditions with varied etiologies.
- Population-based studies are essential for understanding the incidence and risk factors of NE and associated conditions.
Purpose of the Study:
- To investigate the association between term newborn encephalopathy (NE) and the later development of autism spectrum disorders (ASDs).
- To quantify the risk of ASD diagnosis in survivors of NE compared to controls.
- To identify potential long-term neurodevelopmental outcomes following moderate to severe NE.
Main Methods:
- A population-based cohort study in Western Australia involving term newborn infants with NE and randomly selected controls.
- Neurobehavioural and cognitive follow-up assessments at 3 and 5 years of age.
- Diagnosis of ASDs based on DSM-IV criteria, with record linkage to disability services to ensure comprehensive ascertainment.
Main Results:
- Among NE survivors, 5% were diagnosed with an ASD by age 5, compared to 0.8% of controls.
- Children with a history of NE were 5.9 times more likely to be diagnosed with an ASD than controls.
- Mortality rates by age 5 were higher in the NE group (13.4%) compared to controls (0.2%).
Conclusions:
- Term newborn encephalopathy is associated with a significantly increased risk of developing autism spectrum disorders.
- Early identification and intervention for children with NE may be crucial for addressing potential neurodevelopmental challenges, including ASDs.
- Further research into the underlying mechanisms linking NE and ASDs is warranted.
Abstract:
Between June 1993 and December 1996, 276 term newborn infants with encephalopathy and 564 randomly selected term controls were enrolled in a population-based study of moderate and severe term newborn encephalopathy (NE) in Western Australia. During comprehensive neurobehavioural and cognitive follow-up of all patients and controls at 3 years and again at 5 years of age we found an unexpected but strong association between NE and autism spectrum disorders (ASDs). A diagnosis of ASD by age 5 years was reached using criteria according of the Diagnostic Statistical Manual, 4th edition. Linking records to the Western Australian Disability Services Commission Register ensured that no child in the study with ASD was missed. By age 5 years, 37 (13.4%) infants with NE and one (0.2%) control had died. Among the 239 survivors of NE, 12 (5%) were diagnosed with an ASD. Of these, 10 (4.2%) met the full criteria for autism, one had pervasive developmental disorder-not otherwise specified, and one had Asperger syndrome. Among the 563 surviving controls, five (0.8%) were diagnosed with an ASD: three with autism, one with autism/possible Asperger syndrome, and one with Asperger syndrome. Compared with the controls, the children who had experienced NE were 5.9 times (95% confidence interval 2.0-16.9) more likely to have been diagnosed with an ASD.
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