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Testing a clinical staging model for bipolar disorder using longitudinal life chart data
OBJECTIVE: Bipolar disorder has a wide range of clinical manifestations which may progress over time. The aim of this study was to test the applicability of a clinical staging model for bipolar disorder and to gain insight into the nature of the variables influencing progression through consecutive...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590317/ https://www.ncbi.nlm.nih.gov/pubmed/30447123 http://dx.doi.org/10.1111/bdi.12727 |
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author | van der Markt, Afra Klumpers, Ursula MH Draisma, Stasja Dols, Annemiek Nolen, Willem A Post, Robert M Altshuler, Lori L Frye, Mark A Grunze, Heinz Keck, Paul E McElroy, Susan L Suppes, Trisha Beekman, Aartjan TF Kupka, Ralph W |
author_facet | van der Markt, Afra Klumpers, Ursula MH Draisma, Stasja Dols, Annemiek Nolen, Willem A Post, Robert M Altshuler, Lori L Frye, Mark A Grunze, Heinz Keck, Paul E McElroy, Susan L Suppes, Trisha Beekman, Aartjan TF Kupka, Ralph W |
author_sort | van der Markt, Afra |
collection | PubMed |
description | OBJECTIVE: Bipolar disorder has a wide range of clinical manifestations which may progress over time. The aim of this study was to test the applicability of a clinical staging model for bipolar disorder and to gain insight into the nature of the variables influencing progression through consecutive stages. METHODS: Using retrospectively reported longitudinal life chart data of 99 subjects from the Stanley Foundation Bipolar Network Naturalistic Follow‐up Study, the occurrence, duration and timely sequence of stages 2‐4 were determined per month. A multi‐state model was used to calculate progression rates and identify determinants of illness progression. Stages 0, 1 and several other variables were added to the multi‐state model to determine their influence on the progression rates. RESULTS: Five years after onset of BD (stage 2), 72% reached stage 3 (recurrent episodes) and 21% had reached stage 4 (continuous episodes), of whom 8% recovered back to stage 3. The progression from stage 2 to 3 was increased by a biphasic onset for both the depression‐mania and the mania‐depression course and by male sex. CONCLUSIONS: Staging is a useful model to determine illness progression in longitudinal life chart data. Variables influencing transition rates were successfully identified. |
format | Online Article Text |
id | pubmed-6590317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65903172019-07-08 Testing a clinical staging model for bipolar disorder using longitudinal life chart data van der Markt, Afra Klumpers, Ursula MH Draisma, Stasja Dols, Annemiek Nolen, Willem A Post, Robert M Altshuler, Lori L Frye, Mark A Grunze, Heinz Keck, Paul E McElroy, Susan L Suppes, Trisha Beekman, Aartjan TF Kupka, Ralph W Bipolar Disord Research Articles OBJECTIVE: Bipolar disorder has a wide range of clinical manifestations which may progress over time. The aim of this study was to test the applicability of a clinical staging model for bipolar disorder and to gain insight into the nature of the variables influencing progression through consecutive stages. METHODS: Using retrospectively reported longitudinal life chart data of 99 subjects from the Stanley Foundation Bipolar Network Naturalistic Follow‐up Study, the occurrence, duration and timely sequence of stages 2‐4 were determined per month. A multi‐state model was used to calculate progression rates and identify determinants of illness progression. Stages 0, 1 and several other variables were added to the multi‐state model to determine their influence on the progression rates. RESULTS: Five years after onset of BD (stage 2), 72% reached stage 3 (recurrent episodes) and 21% had reached stage 4 (continuous episodes), of whom 8% recovered back to stage 3. The progression from stage 2 to 3 was increased by a biphasic onset for both the depression‐mania and the mania‐depression course and by male sex. CONCLUSIONS: Staging is a useful model to determine illness progression in longitudinal life chart data. Variables influencing transition rates were successfully identified. John Wiley and Sons Inc. 2018-12-12 2019-05 /pmc/articles/PMC6590317/ /pubmed/30447123 http://dx.doi.org/10.1111/bdi.12727 Text en © 2018 The Authors. Bipolar Disorders Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles van der Markt, Afra Klumpers, Ursula MH Draisma, Stasja Dols, Annemiek Nolen, Willem A Post, Robert M Altshuler, Lori L Frye, Mark A Grunze, Heinz Keck, Paul E McElroy, Susan L Suppes, Trisha Beekman, Aartjan TF Kupka, Ralph W Testing a clinical staging model for bipolar disorder using longitudinal life chart data |
title | Testing a clinical staging model for bipolar disorder using longitudinal life chart data |
title_full | Testing a clinical staging model for bipolar disorder using longitudinal life chart data |
title_fullStr | Testing a clinical staging model for bipolar disorder using longitudinal life chart data |
title_full_unstemmed | Testing a clinical staging model for bipolar disorder using longitudinal life chart data |
title_short | Testing a clinical staging model for bipolar disorder using longitudinal life chart data |
title_sort | testing a clinical staging model for bipolar disorder using longitudinal life chart data |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6590317/ https://www.ncbi.nlm.nih.gov/pubmed/30447123 http://dx.doi.org/10.1111/bdi.12727 |
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