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Multi-state models for investigating possible stages leading to bipolar disorder
BACKGROUND: It has been proposed that bipolar disorder onsets in a predictable progressive sequence of clinical stages. However, there is some debate in regard to a statistical approach to test this hypothesis. The objective of this paper is to investigate two different analysis strategies to determ...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4338115/ https://www.ncbi.nlm.nih.gov/pubmed/25713772 http://dx.doi.org/10.1186/s40345-014-0019-4 |
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author | Keown-Stoneman, Charles DG Horrocks, Julie Darlington, Gerarda A Goodday, Sarah Grof, Paul Duffy, Anne |
author_facet | Keown-Stoneman, Charles DG Horrocks, Julie Darlington, Gerarda A Goodday, Sarah Grof, Paul Duffy, Anne |
author_sort | Keown-Stoneman, Charles DG |
collection | PubMed |
description | BACKGROUND: It has been proposed that bipolar disorder onsets in a predictable progressive sequence of clinical stages. However, there is some debate in regard to a statistical approach to test this hypothesis. The objective of this paper is to investigate two different analysis strategies to determine the best suited model to assess the longitudinal progression of clinical stages in the development of bipolar disorder. METHODS: Data previously collected on 229 subjects at high risk of developing bipolar disorder were used for the statistical analysis. We investigate two statistical approaches for analyzing the relationship between the proposed stages of bipolar disorder: 1) the early stages are considered as time-varying covariates affecting the hazard of bipolar disorder in a Cox proportional hazards model, 2) the early stages are explicitly modelled as states in a non-parametric multi-state model. RESULTS: We found from the Cox model thatthere was evidence that the hazard of bipolar disorder is increased by the onset of major depressive disorder. From the multi-state model, in high-risk offspring the probability of bipolar disorder by age 29 was estimated as 0.2321. Cumulative incidence functions representing the probability of bipolar disorder given major depressive disorder at or before age 18 were estimated using both approaches and found to be similar. CONCLUSIONS: Both the Cox model and multi-state model are useful approaches to the modelling of antecedent risk syndromes. They lead to similar cumulative incidence functions but otherwise each method offers a different advantage. |
format | Online Article Text |
id | pubmed-4338115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-43381152015-02-25 Multi-state models for investigating possible stages leading to bipolar disorder Keown-Stoneman, Charles DG Horrocks, Julie Darlington, Gerarda A Goodday, Sarah Grof, Paul Duffy, Anne Int J Bipolar Disord Research BACKGROUND: It has been proposed that bipolar disorder onsets in a predictable progressive sequence of clinical stages. However, there is some debate in regard to a statistical approach to test this hypothesis. The objective of this paper is to investigate two different analysis strategies to determine the best suited model to assess the longitudinal progression of clinical stages in the development of bipolar disorder. METHODS: Data previously collected on 229 subjects at high risk of developing bipolar disorder were used for the statistical analysis. We investigate two statistical approaches for analyzing the relationship between the proposed stages of bipolar disorder: 1) the early stages are considered as time-varying covariates affecting the hazard of bipolar disorder in a Cox proportional hazards model, 2) the early stages are explicitly modelled as states in a non-parametric multi-state model. RESULTS: We found from the Cox model thatthere was evidence that the hazard of bipolar disorder is increased by the onset of major depressive disorder. From the multi-state model, in high-risk offspring the probability of bipolar disorder by age 29 was estimated as 0.2321. Cumulative incidence functions representing the probability of bipolar disorder given major depressive disorder at or before age 18 were estimated using both approaches and found to be similar. CONCLUSIONS: Both the Cox model and multi-state model are useful approaches to the modelling of antecedent risk syndromes. They lead to similar cumulative incidence functions but otherwise each method offers a different advantage. Springer Berlin Heidelberg 2015-02-24 /pmc/articles/PMC4338115/ /pubmed/25713772 http://dx.doi.org/10.1186/s40345-014-0019-4 Text en © Keown-Stoneman et al.; licensee Springer. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. |
spellingShingle | Research Keown-Stoneman, Charles DG Horrocks, Julie Darlington, Gerarda A Goodday, Sarah Grof, Paul Duffy, Anne Multi-state models for investigating possible stages leading to bipolar disorder |
title | Multi-state models for investigating possible stages leading to bipolar disorder |
title_full | Multi-state models for investigating possible stages leading to bipolar disorder |
title_fullStr | Multi-state models for investigating possible stages leading to bipolar disorder |
title_full_unstemmed | Multi-state models for investigating possible stages leading to bipolar disorder |
title_short | Multi-state models for investigating possible stages leading to bipolar disorder |
title_sort | multi-state models for investigating possible stages leading to bipolar disorder |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4338115/ https://www.ncbi.nlm.nih.gov/pubmed/25713772 http://dx.doi.org/10.1186/s40345-014-0019-4 |
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