Abstract

BackgroundIn schizophrenia, a decline in cognitive functioning often precedes the onset of the first psychotic episode by many years. We have previously shown this to be the case for individuals with 22q11.2 deletion syndrome (22q11DS), a genetic variant associated with a 20–25% risk of developing schizophrenia. We also observed that, regardless of the subsequent development of psychosis, individuals with 22q11DS show, on average a modest decline in IQ between 8 and 24 years and that in those who develop a psychotic disorder this decline follows a steeper trajectory. The tendency for a modest cognitive decline may represent a cognitive phenotype that is specific to 22q11DS, and possibly, an endophenotype for schizophrenia in this population. In order to assess this, we constructed a normative chart for cognitive development over time in individuals with 22q11DS.MethodsWe made use of the International Brain and Behavior Consortium on 22q11DS (IBBC) database that includes cross-sectional and longitudinal cognitive data from 1871 individuals with 22q11DS (mean age 15.7, SD 7.4, years; n = 330 (17.6%) with schizophrenia). All IQ measurements were obtained by qualified personnel using Wechsler tests, including WPPSI, WISC and WAIS, depending on the participants’ ages. We used all available IQ data points obtained in the age range 6 - 40 years to construct normative charts for Full Scale IQ (FSIQ), Verbal IQ (VIQ) and Performance IQ (PIQ), after a comprehensive quality control procedure to ensure reliable and comparable IQ data across all international sites. We used a polynomial regression model, similar to what is used in standardized international growth charts for height and weight, to create the normative chart.ResultsThe 4th order polynomial regression provided a good fit for the IQ data from our sample, allowing for the observed larger variability in very young age groups. On average, between the ages of 6 and 40 years, the 22q11DS population showed a gradual, modest decline in FSIQ, VIQ and PIQ. Consistent with our previous results, individuals who went on to develop schizophrenia showed a steeper decline, representing a deviation from their expected trajectory, than those who had no documented psychotic illness.DiscussionThis study is, to our knowledge, the first to demonstrate that a normative chart for cognitive development through to adulthood can be reliably constructed for a genetically selected high-risk population. This normative chart can be readily applied both in clinical care and in research and may serve as an example for constructing similar normative charts in other high-risk groups and/or genetic disorders.

Highlights

  • The incidence of psychotic disorders varies between geographical areas and is associated with neighbourhood characteristics

  • This study will determine whether the incidence of first episode psychosis (FEP) is associated with neighbourhood characteristics, social deprivation, unemployment, social fragmentation and social capital

  • This study was conducted at the Early Psychosis Prevention and Intervention Centre (EPPIC) which provides specialist treatment to all young people aged 15–24 diagnosed with a FEP residing in a defined geographical catchment area within western and northwestern Melbourne

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Summary

Background

People aged 65 and above have consistently been omitted from research on the epidemiology of psychotic disorders. We aimed to characterise the incidence of VLOSLP in a Swedish population cohort, including how incidence varied by age, sex, migration, deprivation, traumatic life events, and social isolation. Methods: We conducted a Swedish population-based cohort study to examine the incidence of VLOSLP by potential environmental risk factors. We used Cox regression to obtain hazard ratios and 95% confidence intervals for VLOSLP by age, sex, migration, disposable income at age 60, and the experience of the death of a partner or child, adjusting for potential confounders. Results: In a cohort of 2,955,796 people, we identified 14,825 cases with VLOSLP, with an overall incidence rate of 38.1 (95% CI: 37.5 – 38.7) per 100,000 person-years at-risk. Rates were higher amongst migrants from North America (HR=1.4, 95% CI=1.0–1.9), Europe (HR=1.5, 95% CI=1.4–1.6), Russian-Baltic regions (HR=1.7, 95% CI=1.4–2) and Africa

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