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Published on: November 21, 2013
Hospital admission with infection during childhood and risk for psychotic illness--a population-based cohort study
Åsa Blomström1, Håkan Karlsson2, Anna Svensson3
1Department of Public Health Sciences, Karolinska Institutet, Stockholm, Sweden; asa.blomstrom@ki.se.
Insights
Childhood infections, especially bacterial and central nervous system infections during preadolescence, are linked to an increased risk of developing nonaffective psychosis later in life. This association highlights potential vulnerabilities during critical developmental periods.
Area of Science:
- Neuroscience
- Psychiatry
- Epidemiology
Background:
- Maternal infections during pregnancy are known risk factors for psychosis.
- The impact of childhood infections on psychosis risk requires further investigation.
- Brain development continues through childhood and adolescence, suggesting potential windows of vulnerability.
Purpose of the Study:
- To examine the association between childhood infections and the risk of developing nonaffective psychosis.
- To identify specific types of infections and age periods during childhood that may confer the highest risk.
Main Methods:
- A large population-based birth cohort in Sweden (N = 1,172,879) was followed from birth until 2006.
- Inclusion criteria involved individuals born between 1973 and 1985, with follow-up for nonaffective psychosis diagnoses from age 14.
- Statistical analyses adjusted for sex, socioeconomic status, family history of psychosis, and non-psychiatric hospital admissions.
Main Results:
- A significant association was found between general childhood infections (0-13 years) and later nonaffective psychosis diagnosis (HR = 1.10).
- Bacterial infections showed a stronger association (HR = 1.23), particularly during preadolescence (10-13 years) (HR = 1.57).
- Central nervous system infections in preadolescence conferred the highest risk (HR = 1.96).
Conclusions:
- Childhood infections, particularly bacterial and CNS infections during preadolescence, are associated with an increased risk of nonaffective psychosis.
- Preadolescence appears to be a critical developmental period for this association.
- Findings may also suggest increased susceptibility to infections in children predisposed to psychosis due to other factors.
Abstract:
A growing body of literature suggests that exposure to infections, particularly maternal infections, during pregnancy confers risk for later development of psychotic disorder. Though brain development proceeds throughout childhood and adolescence, the influence of infections during these ages on subsequent psychosis risk is insufficiently examined. The aim of this study was to investigate the potential association between infections during childhood and nonaffective psychoses in a large population-based birth cohort with follow up long enough to include peak incidence of nonaffective psychosis. We included all individuals born in Sweden between 1973 and 1985, (N = 1172879), with follow up on first time inpatient care with nonaffective psychosis from age 14 years until 2006, (N = 4638). Following adjustment for differences in sex, socioeconomic status, family history of psychosis, and hospital admissions involving noninfectious, nonpsychiatric care, we observed a small but statistically significant association between hospital admissions for infections, in general, throughout childhood (0-13 years) and a later diagnosis of nonaffective psychosis, hazard ratio (HR) = 1.10 (95% CI 1.03-1.18), and this association seemed to be driven by bacterial infection, HR = 1.23 (95% CI 1.08-1.40). Bacterial infections and central nervous system infections during preadolescence (10-13 years) conferred the strongest risk, HR 1.57 (95% CI 1.21-2.05) and HR 1.96 (95% CI 1.05-3.62), respectively. Although preadolescence appeared to be a vulnerable age period, and bacterial infection the most severe in relation to psychosis development, the present findings can also indicate an increased susceptibility to hospital admission for infections among children who will later develop nonaffective psychosis due to social or familial/genetic factors.
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