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A population-based study of atopic disorders and inflammatory markers in childhood before psychotic experiences in
Golam M Khandaker1, Stanley Zammit2, Glyn Lewis3
1Department of Psychiatry, University of Cambridge, UK; Cambridgeshire and Peterborough NHS Foundation Trust, Cambridge, UK; Centre for Mental Health, Addiction and Suicide Research, School of Social and Community Medicine, University of Bristol, UK.
Insights
Childhood atopic disorders like asthma and eczema are linked to a higher risk of adolescent psychotic experiences. However, inflammatory markers did not mediate this association, suggesting other pathways may be involved.
Area of Science:
- Psychiatry
- Immunology
- Developmental Psychology
Background:
- Schizophrenia is linked to atopy and elevated inflammatory markers.
- Childhood atopic disorders may influence later mental health outcomes.
- Understanding early risk factors for psychotic experiences is crucial.
Purpose of the Study:
- To investigate the association between childhood atopic disorders and subsequent psychotic experiences (PEs).
- To examine the role of serum inflammatory markers, interleukin 6 (IL-6) and C-reactive protein (CRP), in this relationship.
- To determine if inflammatory markers mediate the link between atopy and PEs.
Main Methods:
- Population-based longitudinal study design.
- Assessment of PEs at age 13 in 6785 children.
- Determination of childhood atopic disorders (asthma, eczema) at age 10 in 7814 children.
- Measurement of serum IL-6 and CRP at age 9 in 5076 children.
- Logistic and linear regression analyses controlling for confounders.
Main Results:
- Approximately 14% had asthma, 12% eczema, and 7% both at age 10.
- Children with atopic disorders had an increased risk of PEs at age 13 (ORs ranging from 1.33 to 1.44).
- Atopy was associated with higher IL-6 and CRP, but these markers did not mediate the atopy-PEs association.
- Inflammatory markers were not directly associated with later PEs.
Conclusions:
- Childhood atopic disorders are associated with an increased risk of adolescent psychotic experiences.
- The inflammatory pathway (IL-6, CRP) does not appear to mediate this association.
- Further research is needed to explore other mechanisms linking atopy to PEs and their developmental trajectories.
Objective:
Schizophrenia is associated with atopy and increased inflammatory markers. We report a population-based longitudinal study of the associations between childhood atopic disorders, subsequent serum inflammatory markers, interleukin 6 (IL-6) and C-reactive protein (CRP), and the risk of psychotic experiences (PEs).
Method:
PEs were assessed at age 13 years (n=6785). Presence of clinician-diagnosed atopic disorders (asthma and eczema) was determined from parent-completed questionnaires at age 10 years (n=7814). Serum IL-6 and CRP were measured at age 9 years (n=5076). Logistic regression examined the association between (1) atopy and PEs, (2) inflammatory markers and PEs, and (3) mediating effects of inflammatory markers on the atopy-PEs association. Linear regression examined the association between atopy and inflammatory markers. Age, gender, social class, ethnicity and body mass index were included as potential confounders.
Results:
At age 10 years, about 14% of the sample was reported to have asthma, 12% eczema, and 7% both asthma and eczema. Compared with children with no atopy, risk of PEs at age 13 years was increased for all of these groups; adjusted odds ratios (95% CI) were, respectively, 1.39 (1.10-1.77), 1.33 (1.04-1.69), and 1.44 (1.06-1.94). Atopy was associated with increased serum IL-6 and CRP; however, this did not mediate association between atopy and PEs. Inflammatory markers were not associated with later PEs.
Conclusion:
Childhood atopic disorders increase the risk of psychotic experiences in adolescence. Follow-up of these individuals will be useful to determine the effect of atopy and inflammation on different trajectories of early-life PEs.
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