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Characterising symptomatic substates in individuals on the psychosis continuum: a hidden Markov modelling approach

Published online by Cambridge University Press:  12 March 2025

Isabelle Scott*
Affiliation:
Orygen, Parkville, VC, Australia Centre for Youth Mental Health, The University of Melbourne, Melbourne, VIC, Australia
Emmeke Aarts
Affiliation:
Department of Methodology and Statistics, Faculty of Social and Behavioural Sciences, Utrecht University, Utrecht, Netherlands
Cassandra Wannan
Affiliation:
Orygen, Parkville, VC, Australia Centre for Youth Mental Health, The University of Melbourne, Melbourne, VIC, Australia
Caroline X. Gao
Affiliation:
Orygen, Parkville, VC, Australia Centre for Youth Mental Health, The University of Melbourne, Melbourne, VIC, Australia School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia
Scott Clark
Affiliation:
Discipline of Psychiatry, Adelaide Medical School, The University of Adelaide, Adelaide, SA, Australia
Simon Hartmann
Affiliation:
Orygen, Parkville, VC, Australia Centre for Youth Mental Health, The University of Melbourne, Melbourne, VIC, Australia Discipline of Psychiatry, Adelaide Medical School, The University of Adelaide, Adelaide, SA, Australia
Josh Nguyen
Affiliation:
Orygen, Parkville, VC, Australia Centre for Youth Mental Health, The University of Melbourne, Melbourne, VIC, Australia
Blake Cavve
Affiliation:
Telethon Kids Institute, The University of Western Australia, Perth, WA, Australia
Jessica A. Hartmann
Affiliation:
Orygen, Parkville, VC, Australia Centre for Youth Mental Health, The University of Melbourne, Melbourne, VIC, Australia Department of Public Mental Health, Central Institute of Mental Health, Medical Faculty Mannheim, University of Heidelberg, Mannheim, Germany
Dominic Dwyer
Affiliation:
Orygen, Parkville, VC, Australia Centre for Youth Mental Health, The University of Melbourne, Melbourne, VIC, Australia
Sara van der Tuin
Affiliation:
Department of Psychiatry, Interdisciplinary Center Psychopathology and Emotion Regulation, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands
Esdras Raposo de Almeida
Affiliation:
Department of Psychiatry, Interdisciplinary Center Psychopathology and Emotion Regulation, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands Institute & Department of Psychiatry (LIM-23), Hospital das Clinicas, School of Medicine, University of Sao Paulo, Sao Paulo, Brazil
Ashleigh Lin
Affiliation:
School of Population and Global Health, The University of Western Australia, Perth, WA, Australia
G. Paul Amminger
Affiliation:
Orygen, Parkville, VC, Australia Centre for Youth Mental Health, The University of Melbourne, Melbourne, VIC, Australia
Andrew Thompson
Affiliation:
Orygen, Parkville, VC, Australia Centre for Youth Mental Health, The University of Melbourne, Melbourne, VIC, Australia
Stephen J Wood
Affiliation:
Orygen, Parkville, VC, Australia Centre for Youth Mental Health, The University of Melbourne, Melbourne, VIC, Australia School of Psychology, The University of Birmingham, Birmingham, UK
Alison R. Yung
Affiliation:
Institute for Mental and Physical Health and Clinical Translation, Deakin University, Melbourne, VIC, Australia
David van den Berg
Affiliation:
Department of Clinical Psychology, Amsterdam Public Health Research Institute, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands Mark van der Gaag Research Centre, Parnassia Psychiatric Institute, The Hague, The Netherlands
Patrick D. McGorry
Affiliation:
Orygen, Parkville, VC, Australia Centre for Youth Mental Health, The University of Melbourne, Melbourne, VIC, Australia
Johanna T.W. Wigman
Affiliation:
Department of Psychiatry, Interdisciplinary Center Psychopathology and Emotion Regulation, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands
Barnaby Nelson
Affiliation:
Orygen, Parkville, VC, Australia Centre for Youth Mental Health, The University of Melbourne, Melbourne, VIC, Australia
*
Corresponding author: Isabelle Scott; Email: isabelle.scott@orygen.org.au
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Abstract

Background

To improve early intervention and personalise treatment for individuals early on the psychosis continuum, a greater understanding of symptom dynamics is required. We address this by identifying and evaluating the movement between empirically derived attenuated psychotic symptomatic substates—clusters of symptoms that occur within individuals over time.

Methods

Data came from a 90-day daily diary study evaluating attenuated psychotic and affective symptoms. The sample included 96 individuals aged 18–35 on the psychosis continuum, divided into four subgroups of increasing severity based on their psychometric risk of psychosis, with the fourth meeting ultra-high risk (UHR) criteria. A multilevel hidden Markov modelling (HMM) approach was used to characterise and determine the probability of switching between symptomatic substates. Individual substate trajectories and time spent in each substate were subsequently assessed.

Results

Four substates of increasing psychopathological severity were identified: (1) low-grade affective symptoms with negligible psychotic symptoms; (2) low levels of nonbizarre ideas with moderate affective symptoms; (3) low levels of nonbizarre ideas and unusual thought content, with moderate affective symptoms; and (4) moderate levels of nonbizarre ideas, unusual thought content, and affective symptoms. Perceptual disturbances predominantly occurred within the third and fourth substates. UHR individuals had a reduced probability of switching out of the two most severe substates.

Conclusions

Findings suggest that individuals reporting unusual thought content, rather than nonbizarre ideas in isolation, may exhibit symptom dynamics with greater psychopathological severity. Individuals at a higher risk of psychosis exhibited persistently severe symptom dynamics, indicating a potential reduction in psychological flexibility.

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
© The Author(s), 2025. Published by Cambridge University Press
Figure 0

Table 1. Demographic and clinical characteristics of the sample

Figure 1

Figure 1. Group level emission distributions characterizing the four clinical substates uncovered with the multilevel HMM. A continuous multivariate normal distribution captures the most likely scores for each of the six diary items that are observed in each substate.

Figure 2

Figure 2. Substate sequences generated for four individuals across subgroups 1–4. Missing diary data is imputed while missing substate sequence data is displayed in white. The exemplar individual spent: (a) most time in the first substate, consistent with negligible psychotic symptoms; (b) most time in the first and third substates, displaying high affective symptoms throughout the assessment period, with occasional symptoms of broadcasting; (c) multiple days in the fourth substate at the start of the assessment period, displaying high psychotic symptoms during this time. In the middle of the assessment period, this same individual spent periods in the second substate, displaying periods of high affective symptoms and suspiciousness, and, towards the end of the assessment period, spent most time in the first substate, exhibiting minimal psychotic symptoms; (d) most time in the fourth substate, displaying moderate scores for all items across the assessment period.

Figure 3

Figure 3. Perceptual disturbances and temporally associated state sequences for eight individuals belonging to subgroups 2–4. Grey and black lines (top panel) depict whether a perceptual disturbance was present or absent for each day across the 90-day assessment period. Missing state sequence data is displayed in white.

Figure 4

Figure 4. Network diagram of group-level and subgroup substate switching patterns. Switching probabilities are calculated as the posterior mean of estimates generated by the MCMC sampler, excluding the burn-in period. Nodes represent substates, and edges represent relative switching probabilities. The node area is proportional to the probability of an individual remaining in that substate. Edge thickness is proportional to the size of the relative switching probability (dashed: probabilities <.3, grey: probabilities 2–.4, black: probabilities >.4).

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