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Basic self-disturbance trajectories in clinical high risk for psychosis: a one-year follow-up study

Basic self-disturbance (BSD) has been proposed as a driver of symptom development in schizophrenia spectrum disorders (SSDs). In a one-year follow-up of 32 patients (15–30 years) at putative risk for psychosis, we investigated trajectories of BSD levels from baseline to follow-up, and associations b...

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Autores principales: Værnes, Tor Gunnar, Røssberg, Jan Ivar, Melle, Ingrid, Nelson, Barnaby, Romm, Kristin Lie, Møller, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388413/
https://www.ncbi.nlm.nih.gov/pubmed/34783878
http://dx.doi.org/10.1007/s00406-021-01349-6
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author Værnes, Tor Gunnar
Røssberg, Jan Ivar
Melle, Ingrid
Nelson, Barnaby
Romm, Kristin Lie
Møller, Paul
author_facet Værnes, Tor Gunnar
Røssberg, Jan Ivar
Melle, Ingrid
Nelson, Barnaby
Romm, Kristin Lie
Møller, Paul
author_sort Værnes, Tor Gunnar
collection PubMed
description Basic self-disturbance (BSD) has been proposed as a driver of symptom development in schizophrenia spectrum disorders (SSDs). In a one-year follow-up of 32 patients (15–30 years) at putative risk for psychosis, we investigated trajectories of BSD levels from baseline to follow-up, and associations between clinical characteristics at baseline and follow-up, including follow-up levels of BSD (assessed with the EASE). Clinical high risk (CHR) for psychosis status and symptom severity were assessed with the SIPS/SOPS scales and also according to the cognitive basic symptoms high-risk criteria (COGDIS). DSM-IV diagnoses, functioning and other clinical characteristics were assessed with standard clinical instruments. Higher severity of negative symptoms and meeting COGDIS criteria at baseline were associated with higher BSD levels at follow-up. All measured at follow-up, higher BSD levels correlated with higher severity of positive, negative, disorganization and general symptoms, and with a lower level of global functioning. We found higher BSD levels at follow-up in subjects with schizotypal personality disorder (SPD) at baseline (n = 5) and in SSDs at follow-up (n = 12, including nine with SPD). Mean BSD levels decreased significantly from baseline to follow-up, but individual trajectories varied considerably. Increased BSD levels were associated with higher baseline BSD levels, non-remission of positive symptoms and functional decline. Overall, the current study indicates that subgroups in the CHR population with a higher risk of non-remission or deterioration may be identified by supplementing CHR criteria with assessment of BSD and negative symptoms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00406-021-01349-6.
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spelling pubmed-93884132022-08-20 Basic self-disturbance trajectories in clinical high risk for psychosis: a one-year follow-up study Værnes, Tor Gunnar Røssberg, Jan Ivar Melle, Ingrid Nelson, Barnaby Romm, Kristin Lie Møller, Paul Eur Arch Psychiatry Clin Neurosci Original Paper Basic self-disturbance (BSD) has been proposed as a driver of symptom development in schizophrenia spectrum disorders (SSDs). In a one-year follow-up of 32 patients (15–30 years) at putative risk for psychosis, we investigated trajectories of BSD levels from baseline to follow-up, and associations between clinical characteristics at baseline and follow-up, including follow-up levels of BSD (assessed with the EASE). Clinical high risk (CHR) for psychosis status and symptom severity were assessed with the SIPS/SOPS scales and also according to the cognitive basic symptoms high-risk criteria (COGDIS). DSM-IV diagnoses, functioning and other clinical characteristics were assessed with standard clinical instruments. Higher severity of negative symptoms and meeting COGDIS criteria at baseline were associated with higher BSD levels at follow-up. All measured at follow-up, higher BSD levels correlated with higher severity of positive, negative, disorganization and general symptoms, and with a lower level of global functioning. We found higher BSD levels at follow-up in subjects with schizotypal personality disorder (SPD) at baseline (n = 5) and in SSDs at follow-up (n = 12, including nine with SPD). Mean BSD levels decreased significantly from baseline to follow-up, but individual trajectories varied considerably. Increased BSD levels were associated with higher baseline BSD levels, non-remission of positive symptoms and functional decline. Overall, the current study indicates that subgroups in the CHR population with a higher risk of non-remission or deterioration may be identified by supplementing CHR criteria with assessment of BSD and negative symptoms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00406-021-01349-6. Springer Berlin Heidelberg 2021-11-16 2022 /pmc/articles/PMC9388413/ /pubmed/34783878 http://dx.doi.org/10.1007/s00406-021-01349-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Værnes, Tor Gunnar
Røssberg, Jan Ivar
Melle, Ingrid
Nelson, Barnaby
Romm, Kristin Lie
Møller, Paul
Basic self-disturbance trajectories in clinical high risk for psychosis: a one-year follow-up study
title Basic self-disturbance trajectories in clinical high risk for psychosis: a one-year follow-up study
title_full Basic self-disturbance trajectories in clinical high risk for psychosis: a one-year follow-up study
title_fullStr Basic self-disturbance trajectories in clinical high risk for psychosis: a one-year follow-up study
title_full_unstemmed Basic self-disturbance trajectories in clinical high risk for psychosis: a one-year follow-up study
title_short Basic self-disturbance trajectories in clinical high risk for psychosis: a one-year follow-up study
title_sort basic self-disturbance trajectories in clinical high risk for psychosis: a one-year follow-up study
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388413/
https://www.ncbi.nlm.nih.gov/pubmed/34783878
http://dx.doi.org/10.1007/s00406-021-01349-6
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