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Time‐course of clinical symptoms in young people at ultra‐high risk for transition to psychosis

BACKGROUND: Ultra‐high risk (UHR) people are a heterogeneous group with variable outcomes. This study aimed at (a) estimating trajectories of response to treatment to identify homogeneous subgroups; (b) establishing the impact on these trajectories of known predictors of outcome in UHR subjects. MET...

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Autores principales: Meneghelli, Anna, Cocchi, Angelo, Meliante, Maria, Barbera, Simona, Malvini, Lara, Monzani, Emiliano, Preti, Antonio, Percudani, Mauro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543341/
https://www.ncbi.nlm.nih.gov/pubmed/34296524
http://dx.doi.org/10.1111/eip.13201
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author Meneghelli, Anna
Cocchi, Angelo
Meliante, Maria
Barbera, Simona
Malvini, Lara
Monzani, Emiliano
Preti, Antonio
Percudani, Mauro
author_facet Meneghelli, Anna
Cocchi, Angelo
Meliante, Maria
Barbera, Simona
Malvini, Lara
Monzani, Emiliano
Preti, Antonio
Percudani, Mauro
author_sort Meneghelli, Anna
collection PubMed
description BACKGROUND: Ultra‐high risk (UHR) people are a heterogeneous group with variable outcomes. This study aimed at (a) estimating trajectories of response to treatment to identify homogeneous subgroups; (b) establishing the impact on these trajectories of known predictors of outcome in UHR subjects. METHODS: Mixed models of growth curves and latent class growth analysis (LCGA) were applied to the 24‐item brief psychiatric rating scale (BPRS) to measure the response to treatment over 2 years in 125 UHR participants. Group differences were tested on sociodemographic variables and clinical indicators that are known to affect the outcome in UHR people. RESULTS: BPRS scores decreased across all tested models, with a greater decrease for affective and positive symptoms than for all other dimensions of BPRS. Past admissions to the hospital for psychiatric reasons other than psychosis and the presence of a decline in premorbid functioning before the episode were associated with a slower decrease of BPRS score. LCGA identified three classes, one (82% of participants) with a progressive decrease in the BPRS scores, a second class with a moderate improvement (10%), and a third with no improvement (8%). Those in the ‘no improvement’ class had a higher chance of receiving a diagnosis of psychosis within the spectrum of schizophrenia. CONCLUSION: Most UHR individuals that are treated within a specialized service undergo substantial improvement in their psychopathology, but some seem resistant to the protocol of treatment and need close reevaluation within the first 12 months of treatment.
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spelling pubmed-95433412022-10-14 Time‐course of clinical symptoms in young people at ultra‐high risk for transition to psychosis Meneghelli, Anna Cocchi, Angelo Meliante, Maria Barbera, Simona Malvini, Lara Monzani, Emiliano Preti, Antonio Percudani, Mauro Early Interv Psychiatry Original Articles BACKGROUND: Ultra‐high risk (UHR) people are a heterogeneous group with variable outcomes. This study aimed at (a) estimating trajectories of response to treatment to identify homogeneous subgroups; (b) establishing the impact on these trajectories of known predictors of outcome in UHR subjects. METHODS: Mixed models of growth curves and latent class growth analysis (LCGA) were applied to the 24‐item brief psychiatric rating scale (BPRS) to measure the response to treatment over 2 years in 125 UHR participants. Group differences were tested on sociodemographic variables and clinical indicators that are known to affect the outcome in UHR people. RESULTS: BPRS scores decreased across all tested models, with a greater decrease for affective and positive symptoms than for all other dimensions of BPRS. Past admissions to the hospital for psychiatric reasons other than psychosis and the presence of a decline in premorbid functioning before the episode were associated with a slower decrease of BPRS score. LCGA identified three classes, one (82% of participants) with a progressive decrease in the BPRS scores, a second class with a moderate improvement (10%), and a third with no improvement (8%). Those in the ‘no improvement’ class had a higher chance of receiving a diagnosis of psychosis within the spectrum of schizophrenia. CONCLUSION: Most UHR individuals that are treated within a specialized service undergo substantial improvement in their psychopathology, but some seem resistant to the protocol of treatment and need close reevaluation within the first 12 months of treatment. Wiley Publishing Asia Pty Ltd 2021-07-22 2022-06 /pmc/articles/PMC9543341/ /pubmed/34296524 http://dx.doi.org/10.1111/eip.13201 Text en © 2021 The Authors. Early Intervention in Psychiatry published by John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Meneghelli, Anna
Cocchi, Angelo
Meliante, Maria
Barbera, Simona
Malvini, Lara
Monzani, Emiliano
Preti, Antonio
Percudani, Mauro
Time‐course of clinical symptoms in young people at ultra‐high risk for transition to psychosis
title Time‐course of clinical symptoms in young people at ultra‐high risk for transition to psychosis
title_full Time‐course of clinical symptoms in young people at ultra‐high risk for transition to psychosis
title_fullStr Time‐course of clinical symptoms in young people at ultra‐high risk for transition to psychosis
title_full_unstemmed Time‐course of clinical symptoms in young people at ultra‐high risk for transition to psychosis
title_short Time‐course of clinical symptoms in young people at ultra‐high risk for transition to psychosis
title_sort time‐course of clinical symptoms in young people at ultra‐high risk for transition to psychosis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543341/
https://www.ncbi.nlm.nih.gov/pubmed/34296524
http://dx.doi.org/10.1111/eip.13201
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