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Do prospective longitudinal studies of bipolar disorder support the hypothesis of neuroprogression?

INTRODUCTION: Bipolar I disorder is a mental disorder with the risk of severe clinical outcomes. Bipolar disorder was initially defined based on having a better outcome than schizophrenia. However, while recent longer-term findings in schizophrenia do not support neuroprogression, bipolar disorder i...

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Autores principales: Melle, I., Lagerberg, T. V., Etain, B., Lyngstad, S. H., Wold, K. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10596672/
http://dx.doi.org/10.1192/j.eurpsy.2023.468
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author Melle, I.
Lagerberg, T. V.
Etain, B.
Lyngstad, S. H.
Wold, K. F.
author_facet Melle, I.
Lagerberg, T. V.
Etain, B.
Lyngstad, S. H.
Wold, K. F.
author_sort Melle, I.
collection PubMed
description INTRODUCTION: Bipolar I disorder is a mental disorder with the risk of severe clinical outcomes. Bipolar disorder was initially defined based on having a better outcome than schizophrenia. However, while recent longer-term findings in schizophrenia do not support neuroprogression, bipolar disorder is increasingly depicted as having neuroprogressive elements. There are, however, remarkably few prospective longitudinal studies of representative bipolar I cohorts followed from the first treatment. OBJECTIVES: To study the clinical development of a representative cohort of bipolar disorder patients recruited at their first treatment. METHODS: Patients with DSM-IV Bipolar I or Bipolar NOS were consecutively recruited from in-and outpatient units in the larger Oslo area during their first treatment year and extensively clinically characterized at baseline. They then participated in personal one- and ten-year follow-ups. RESULTS: Sixty-nine patients participated in the 10-year follow-up. Age at follow-up was 39.0 (+ 9.6) years, 59% were females. A total of 12% had unipolar mania, 58% had psychotic bipolar disorder, and 20% had experienced rapid cycling. At follow-up, 75% were in full affective remission, 60% had regained full functioning, and 54% were in stable full recovery. Mood episode relapses clustered around the first episode. Despite occasional relapses, 2/3 were mainly euthymic during the follow-up period. A small sub-group was highly affected from the first 2-3 years of treatment, but there were no apparent signs of kindling effects or indications of neuroprogression CONCLUSIONS: The follow-up of this cohort of first-treatment Bipolar I patients does not support the hypothesis of neuroprogression. DISCLOSURE OF INTEREST: None Declared
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spelling pubmed-105966722023-10-25 Do prospective longitudinal studies of bipolar disorder support the hypothesis of neuroprogression? Melle, I. Lagerberg, T. V. Etain, B. Lyngstad, S. H. Wold, K. F. Eur Psychiatry Abstract INTRODUCTION: Bipolar I disorder is a mental disorder with the risk of severe clinical outcomes. Bipolar disorder was initially defined based on having a better outcome than schizophrenia. However, while recent longer-term findings in schizophrenia do not support neuroprogression, bipolar disorder is increasingly depicted as having neuroprogressive elements. There are, however, remarkably few prospective longitudinal studies of representative bipolar I cohorts followed from the first treatment. OBJECTIVES: To study the clinical development of a representative cohort of bipolar disorder patients recruited at their first treatment. METHODS: Patients with DSM-IV Bipolar I or Bipolar NOS were consecutively recruited from in-and outpatient units in the larger Oslo area during their first treatment year and extensively clinically characterized at baseline. They then participated in personal one- and ten-year follow-ups. RESULTS: Sixty-nine patients participated in the 10-year follow-up. Age at follow-up was 39.0 (+ 9.6) years, 59% were females. A total of 12% had unipolar mania, 58% had psychotic bipolar disorder, and 20% had experienced rapid cycling. At follow-up, 75% were in full affective remission, 60% had regained full functioning, and 54% were in stable full recovery. Mood episode relapses clustered around the first episode. Despite occasional relapses, 2/3 were mainly euthymic during the follow-up period. A small sub-group was highly affected from the first 2-3 years of treatment, but there were no apparent signs of kindling effects or indications of neuroprogression CONCLUSIONS: The follow-up of this cohort of first-treatment Bipolar I patients does not support the hypothesis of neuroprogression. DISCLOSURE OF INTEREST: None Declared Cambridge University Press 2023-07-19 /pmc/articles/PMC10596672/ http://dx.doi.org/10.1192/j.eurpsy.2023.468 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Melle, I.
Lagerberg, T. V.
Etain, B.
Lyngstad, S. H.
Wold, K. F.
Do prospective longitudinal studies of bipolar disorder support the hypothesis of neuroprogression?
title Do prospective longitudinal studies of bipolar disorder support the hypothesis of neuroprogression?
title_full Do prospective longitudinal studies of bipolar disorder support the hypothesis of neuroprogression?
title_fullStr Do prospective longitudinal studies of bipolar disorder support the hypothesis of neuroprogression?
title_full_unstemmed Do prospective longitudinal studies of bipolar disorder support the hypothesis of neuroprogression?
title_short Do prospective longitudinal studies of bipolar disorder support the hypothesis of neuroprogression?
title_sort do prospective longitudinal studies of bipolar disorder support the hypothesis of neuroprogression?
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10596672/
http://dx.doi.org/10.1192/j.eurpsy.2023.468
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