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Published on: September 27, 2017
Atopic dermatitis and risk of major neuropsychiatric disorders in children: A population-based cohort study
Joy Wan1, Daniel B Shin2, Maha N Syed2
1Department of Dermatology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Insights
Paediatric atopic dermatitis (AD) showed no significant overall risk for most childhood neuropsychiatric conditions. However, AD severity and age may influence outcomes, warranting further research into this complex relationship.
Area of Science:
- Pediatric Dermatology
- Child and Adolescent Psychiatry
- Epidemiology
Background:
- Paediatric atopic dermatitis (AD) is associated with neuropsychiatric comorbidities like depression, anxiety, and ADHD.
- Limited longitudinal data exist, and the impact of AD severity on these outcomes needs further investigation.
Purpose of the Study:
- To investigate the risk of major neuropsychiatric conditions in children diagnosed with atopic dermatitis.
Main Methods:
- A UK population-based cohort study analyzed health records of children under 18 with AD.
- Patients with AD were matched to unaffected controls, with AD severity proxied by treatments.
- Outcomes included incident anxiety, depression, ADHD, autism, OCD, bipolar disorder, schizophrenia, and suicidal behaviors.
Main Results:
- No significant increased risk for anxiety, ADHD, autism, bipolar disorder, or suicidal ideation/attempt was found in children with AD.
- Children with AD showed a decreased risk of depression and schizophrenia but an increased risk of obsessive-compulsive disorder (OCD).
- Significant variations in risk and effect magnitude were observed based on AD severity and patient age.
Conclusions:
- Overall, paediatric atopic dermatitis does not substantially increase the risk for many neuropsychiatric conditions.
- Disease severity and age are potential key factors modifying the relationship between AD and neuropsychiatric comorbidities.
- Further research is essential to fully understand the intricate links between paediatric AD and neuropsychiatric conditions.
Background:
Paediatric atopic dermatitis (AD) has been linked to neuropsychiatric comorbidities such as depression, anxiety and attention-deficit/hyperactivity disorder (ADHD). However, longitudinal data are limited, and the effect of AD severity on neuropsychiatric outcomes requires further characterization.
Objectives:
To determine the risk of several major neuropsychiatric conditions in children with AD.
Methods:
We analysed UK health records data in a population-based cohort study. Each patient <18 years old with AD was matched to up to five unaffected patients on age, practice and index date. Treatments served as proxies for AD severity, which was analysed in a time-updated manner. Outcomes were incident anxiety, depression, bipolar disorder, schizophrenia, ADHD, autism, obsessive-compulsive disorder (OCD), suicidal ideation or attempt, and completed suicide.
Results:
A total of 409,431 children with AD (93.2% mild, 5.5% moderate, 1.3% severe) were compared to 1,809,029 children without AD. In Cox regression models adjusted for age, sex, socioeconomic status and other atopic comorbidities, no statistically significant relationships were observed between AD and incident anxiety (HR 1.01, 95% CI 0.99-1.03), ADHD (1.02, 0.97-1.06), autism (1.02, 0.98-1.06), bipolar disorder (1.08, 0.85-1.36), suicidal ideation/attempt (0.98, 0.95-1.01) or completed suicide (0.85, 0.64-1.14). Children with AD were less likely to develop depression (0.93, 0.91-0.95) or schizophrenia (0.72, 0.54-0.95) but more likely to develop OCD (1.26, 1.16-1.37). However, there was substantial variation by AD severity and age in both the direction and magnitude of effect for many of the neuropsychiatric conditions examined.
Conclusions:
The was no substantial impact of AD on the overall risk of many neuropsychiatric conditions in children, but disease severity and age may be important modifying factors. Additional research is needed to further dissect the complex relationship between paediatric AD and neuropsychiatric comorbidities.
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