Abstract

Childhood infections are associated with adult psychosis and depression, but studies of psychotic experiences (PEs) and depressive symptoms in childhood, adolescence, and early-adulthood are scarce. Previous studies have typically examined severe infections, but studies of common infections are also scarce. Using data from the Avon Longitudinal Study of Parents and Children (ALSPAC) birth cohort, we examined associations of the number of infections in childhood from age 1.5 to 7.5 years with depressive symptom scores at age 10, 13, 14, 17, 18, and 19 years, and with PEs at 12 and 18 years. We performed additional analysis using infection burden ('low' = 0-4 infections, 'medium' = 5-6, 'high' = 7-9, or 'very high' = 10-22 infections) as the exposure. The risk set comprised 11 786 individuals with childhood infection data. Number of childhood infections was associated with depressive symptoms from age 10 (adjusted beta = 0.14; standard error (s.e.) = 0.04; p = <0.01) to 17 years (adjusted beta = 0.17; s.e. = 0.08; p = 0.04), and with PEs at age 12 (suspected/definite PEs: adjusted odds ratio (OR) = 1.18; 95% confidence interval (CI) = 1.09-1.27). These effect sizes were larger when the exposure was defined as very high infection burden (depressive symptoms age 17: adjusted beta = 0.79; s.e. = 0.29; p = 0.01; suspected/definite PEs at age 12: adjusted OR = 1.60; 95% CI = 1.25-2.05). Childhood infections were not associated with depressive/psychotic outcomes at age 18 or 19. Common early-childhood infections are associated with depressive symptoms up to mid-adolescence and with PEs subsequently in childhood, but not with these outcomes in early-adulthood. These findings require replication including larger samples with outcomes in adulthood.

Highlights

  • Early-life infections are associated with an increased risk of serious mental health disorders in adulthood

  • There is an extensive literature linking prenatal maternal and childhood infections with schizophrenia and related psychotic disorders, which are associated with both central nervous system (CNS) and non-CNS infections (Benros et al, 2011; Brown & Derkits, 2010; Dalman et al, 2008; Khandaker et al, 2018; Khandaker, Zimbron, Dalman, Lewis, & Jones, 2012; Khandaker, Zimbron, Lewis, & Jones, 2013)

  • Using data from the Avon Longitudinal Study of Parents and Children (ALSPAC) (Boyd et al, 2013), a general populationrepresentative prospective British birth cohort, we have investigated the longitudinal associations of childhood infections from age 1.5 to 7.5 years old with depressive symptoms measured six times from age 10 to 19 years and with psychotic experiences (PEs) at age 12 and 18 years

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Summary

Introduction

Early-life infections are associated with an increased risk of serious mental health disorders in adulthood. Longitudinal studies of depressive and psychotic experiences (PEs) during childhood/adolescence are scarce (Goodwin, 2011). Population-based longitudinal studies suggest association between early-life PEs with the risk of psychotic disorders subsequently. Childhood infections are associated with adult psychosis and depression, but studies of psychotic experiences (PEs) and depressive symptoms in childhood, adolescence, and early-adulthood are scarce. = 0.08; p = 0.04), and with PEs at age 12 (suspected/definite PEs: adjusted odds ratio (OR) = 1.18; 95% confidence interval (CI) = 1.09–1.27) These effect sizes were larger when the exposure was defined as very high infection burden Common early-childhood infections are associated with depressive symptoms up to mid-adolescence and with PEs subsequently in childhood, but not with these outcomes in early-adulthood. These findings require replication including larger samples with outcomes in adulthood

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