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Enriching ultra-high risk for psychosis cohorts based on accumulated exposure to environmental risk factors for psychotic disorders

Published online by Cambridge University Press:  25 November 2024

Brian O'Donoghue*
Affiliation:
Department of Psychiatry, University College Dublin, Dublin, Ireland Department of Psychiatry, Royal College of Surgeons, Dublin, Ireland Orygen, Parkville, Melbourne, VIC 3052, Australia Centre for Youth Mental Health, University of Melbourne, Melbourne, Australia
Dominic Oliver
Affiliation:
Department of Psychiatry, University of Oxford, Oxford, UK NIHR Oxford Health Biomedical Research Centre, Oxford, UK OPEN Early Detection Service, Oxford Health NHS Foundation Trust, Oxford, UK
Hellen Geros
Affiliation:
Orygen, Parkville, Melbourne, VIC 3052, Australia Centre for Youth Mental Health, University of Melbourne, Melbourne, Australia
Holly Sizer
Affiliation:
Orygen, Parkville, Melbourne, VIC 3052, Australia Centre for Youth Mental Health, University of Melbourne, Melbourne, Australia
Andrew Thompson
Affiliation:
Orygen, Parkville, Melbourne, VIC 3052, Australia Centre for Youth Mental Health, University of Melbourne, Melbourne, Australia
Patrick McGorry
Affiliation:
Orygen, Parkville, Melbourne, VIC 3052, Australia Centre for Youth Mental Health, University of Melbourne, Melbourne, Australia
Barnaby Nelson
Affiliation:
Orygen, Parkville, Melbourne, VIC 3052, Australia Centre for Youth Mental Health, University of Melbourne, Melbourne, Australia
*
Corresponding author: Brian O'Donoghue; Email: brian.odonoghue@ucd.ie
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Abstract

Background and hypothesis

Transition to psychosis rates within ultra-high risk (UHR) services have been declining. It may be possible to ‘enrich’ UHR cohorts based on the environmental characteristics seen more commonly in first-episode psychosis cohorts. This study aimed to determine whether transition rates varied according to the accumulated exposure to environmental risk factors at the individual (migrant status, asylum seeker/refugee status, indigenous population, cannabis/methamphetamine use), family (family history or parental separation), and neighborhood (population density, social deprivation, and fragmentation) level.

Methods

The study included UHR people aged 15–24 who attended the PACE clinic from 2012 to 2016. Cox proportional hazards models (frequentist and Bayesian) were used to assess the association between individual and accumulated factors and transition to psychosis. UHR status and transition was determined using the CAARMS. Benjamini–Hochberg was used to correct for multiple comparisons in frequentist analyses.

Results

Of the 461 young people included, 55.5% were female and median follow-up was 307 days (IQR: 188–557) and 17.6% (n = 81) transitioned to a psychotic disorder. The proportion who transitioned increased incrementally according to the number of individual-level risk factors present (HR = 1.51, 95% CIs 1.19–1.93, p < 0.001, pcorr = 0.01). The number of family- and neighborhood-level exposures did not increase transition risk (p > 0.05). Cannabis use was the only specific risk factor significantly associated with transition (HR = 1.89, 95% CIs 1.22–2.93, pcorr = 0.03, BF = 6.74).

Conclusions

There is a dose–response relationship between exposure to individual-level psychosis-related environmental risk factors and transition risk in UHR patients. If replicated, this could be incorporated into a novel approach to identifying the highest-risk individuals within clinical services.

Information

Type
Original Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
Copyright © The Author(s), 2024. Published by Cambridge University Press
Figure 0

Table 1. Demographic and clinical characteristics

Figure 1

Figure 1. Kaplan–Meier survival curve showing cumulative probability of transition to psychosis with Greenwood 95% confidence intervals. The number at risk at each timepoint presented below refers to the number of individuals who are no longer being followed-up, either due to transition to psychosis or censoring.

Figure 2

Figure 2. Results of Bayesian inference of Cox proportional hazard models for each environmental risk factor. 0.1 < Bayes Factor (BF) < 0.333, moderate evidence for the null hypothesis (H0; no increase in transition risk with exposure to risk factor); 0.333 < BF < 1, weak evidence for the null hypothesis (H0; no increase in transition risk with exposure to risk factor); 1 < BF < 3, weak evidence for the alternative hypothesis (H1; increased transition risk with exposure to risk factor); 3 < BF < 10, moderate evidence for the null hypothesis (H1; increased transition risk with exposure to risk factor).

Figure 3

Table 2. Proportion and hazard ratios for transition according to the number of environmental risk factors

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