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Heterogeneous early illness courses of Korean patients with bipolar disorders: replication of the staging model

BACKGROUND: Clinical staging of bipolar disorder (BD) requires application of real-world data, as the next step in hypothesis. This study used the staging model to analyze the long-term course of BD in Korean patients based on clinical features and treatment responses to map the progression of bipol...

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Autores principales: Lee, Yejin, Lee, Dongbin, Jung, Hyewon, Cho, Yunji, Baek, Ji Hyun, Hong, Kyung Sue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636704/
https://www.ncbi.nlm.nih.gov/pubmed/36333702
http://dx.doi.org/10.1186/s12888-022-04318-y
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author Lee, Yejin
Lee, Dongbin
Jung, Hyewon
Cho, Yunji
Baek, Ji Hyun
Hong, Kyung Sue
author_facet Lee, Yejin
Lee, Dongbin
Jung, Hyewon
Cho, Yunji
Baek, Ji Hyun
Hong, Kyung Sue
author_sort Lee, Yejin
collection PubMed
description BACKGROUND: Clinical staging of bipolar disorder (BD) requires application of real-world data, as the next step in hypothesis. This study used the staging model to analyze the long-term course of BD in Korean patients based on clinical features and treatment responses to map the progression of bipolar illness from its early phase after the onset of illness. METHODS: A total of 136 patients diagnosed with BD-I (n = 62) or BD-II (n = 74) were recruited. Their progressive stages were retrospectively evaluated. A multi-state model was used to calculate the probability of progression to each stage. Hazard ratios of covariates expected to influence different courses of BD were calculated. Using the Alda score, long-term responses to mood stabilizers depending on the current stage were compared. RESULTS: Several sub-populations showed varied courses during the first five years after the onset of illness, with 41.5% remaining in stage 2 and 53% progressing to higher stages with shortened time for transition. Profiles of patients with BD-I and BD-II were different, suggesting biologically distinct groups. Comorbid psychiatric disorders, such as obsessive-compulsive disorder (OCD) and bulimia nervosa (BN) were associated with a recurrent course (stage 3a or 3b) or a malignant course (stage 3c or 4). Early age of onset, shorter duration of illness, older age at the start of medication, and poor response to lithium affected the illness progression. CONCLUSION: We were able to apply the stage model based on episode recurrence patterns in early illness courses of Korean patients with BD. The stage progression pattern differed from the early phase in BD-I and BD-II patients. Psychotic comorbidity, age at onset, age at starting psychiatric treatment showed associations with the illness progression.
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spelling pubmed-96367042022-11-06 Heterogeneous early illness courses of Korean patients with bipolar disorders: replication of the staging model Lee, Yejin Lee, Dongbin Jung, Hyewon Cho, Yunji Baek, Ji Hyun Hong, Kyung Sue BMC Psychiatry Research BACKGROUND: Clinical staging of bipolar disorder (BD) requires application of real-world data, as the next step in hypothesis. This study used the staging model to analyze the long-term course of BD in Korean patients based on clinical features and treatment responses to map the progression of bipolar illness from its early phase after the onset of illness. METHODS: A total of 136 patients diagnosed with BD-I (n = 62) or BD-II (n = 74) were recruited. Their progressive stages were retrospectively evaluated. A multi-state model was used to calculate the probability of progression to each stage. Hazard ratios of covariates expected to influence different courses of BD were calculated. Using the Alda score, long-term responses to mood stabilizers depending on the current stage were compared. RESULTS: Several sub-populations showed varied courses during the first five years after the onset of illness, with 41.5% remaining in stage 2 and 53% progressing to higher stages with shortened time for transition. Profiles of patients with BD-I and BD-II were different, suggesting biologically distinct groups. Comorbid psychiatric disorders, such as obsessive-compulsive disorder (OCD) and bulimia nervosa (BN) were associated with a recurrent course (stage 3a or 3b) or a malignant course (stage 3c or 4). Early age of onset, shorter duration of illness, older age at the start of medication, and poor response to lithium affected the illness progression. CONCLUSION: We were able to apply the stage model based on episode recurrence patterns in early illness courses of Korean patients with BD. The stage progression pattern differed from the early phase in BD-I and BD-II patients. Psychotic comorbidity, age at onset, age at starting psychiatric treatment showed associations with the illness progression. BioMed Central 2022-11-04 /pmc/articles/PMC9636704/ /pubmed/36333702 http://dx.doi.org/10.1186/s12888-022-04318-y Text en © The Author(s) 2022 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Lee, Yejin
Lee, Dongbin
Jung, Hyewon
Cho, Yunji
Baek, Ji Hyun
Hong, Kyung Sue
Heterogeneous early illness courses of Korean patients with bipolar disorders: replication of the staging model
title Heterogeneous early illness courses of Korean patients with bipolar disorders: replication of the staging model
title_full Heterogeneous early illness courses of Korean patients with bipolar disorders: replication of the staging model
title_fullStr Heterogeneous early illness courses of Korean patients with bipolar disorders: replication of the staging model
title_full_unstemmed Heterogeneous early illness courses of Korean patients with bipolar disorders: replication of the staging model
title_short Heterogeneous early illness courses of Korean patients with bipolar disorders: replication of the staging model
title_sort heterogeneous early illness courses of korean patients with bipolar disorders: replication of the staging model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9636704/
https://www.ncbi.nlm.nih.gov/pubmed/36333702
http://dx.doi.org/10.1186/s12888-022-04318-y
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