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All-cause and cause-specific mortality among people with bipolar disorder: a large-scale systematic review and meta-analysis

OBJECTIVE: Bipolar disorder (BD) is associated with premature mortality. All-cause and specific mortality risks in this population remain unclear, and more studies are still needed to further understand this issue and guide individual and public strategies to prevent mortality in bipolar disorder Th...

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Autores principales: Biazus, Taís Boeira, Beraldi, Gabriel Henrique, Tokeshi, Lucas, Rotenberg, Luísa de Siqueira, Dragioti, Elena, Carvalho, André F., Solmi, Marco, Lafer, Beny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10611575/
https://www.ncbi.nlm.nih.gov/pubmed/37491460
http://dx.doi.org/10.1038/s41380-023-02109-9
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author Biazus, Taís Boeira
Beraldi, Gabriel Henrique
Tokeshi, Lucas
Rotenberg, Luísa de Siqueira
Dragioti, Elena
Carvalho, André F.
Solmi, Marco
Lafer, Beny
author_facet Biazus, Taís Boeira
Beraldi, Gabriel Henrique
Tokeshi, Lucas
Rotenberg, Luísa de Siqueira
Dragioti, Elena
Carvalho, André F.
Solmi, Marco
Lafer, Beny
author_sort Biazus, Taís Boeira
collection PubMed
description OBJECTIVE: Bipolar disorder (BD) is associated with premature mortality. All-cause and specific mortality risks in this population remain unclear, and more studies are still needed to further understand this issue and guide individual and public strategies to prevent mortality in bipolar disorder Thus, a systematic review and meta‐analysis of studies assessing mortality risk in people with BD versus the general population was conducted. The primary outcome was all‐cause mortality, whilst secondary outcomes were mortality due to suicide, natural, unnatural, and specific‐causes mortality. RESULTS: Fifty-seven studies were included (BD; n = 678,353). All‐cause mortality was increased in people with BD (RR = 2.02, 95% CI: 1.89–2.16, k = 39). Specific‐cause mortality was highest for suicide (RR = 11.69, 95% CI: 9.22–14.81, k = 25). Risk of death due to unnatural causes (RR = 7.29, 95% CI: 6.41–8.28, k = 17) and natural causes (RR = 1.90, 95% CI: 1.75–2.06, k = 17) were also increased. Among specific natural causes analyzed, infectious causes had the higher RR (RR = 4,38, 95%CI: 1.5–12.69, k = 3), but the analysis was limited by the inclusion of few studies. Mortality risk due to respiratory (RR = 3.18, 95% CI: 2.55–3.96, k = 6), cardiovascular (RR = 1.76, 95% CI: 1.53–2.01, k = 27), and cerebrovascular (RR = 1.57, 95% CI: 1.34–1.84, k = 13) causes were increased as well. No difference was identified in mortality by cancer (RR = 0.99, 95% CI: 0.88–1.11, k = 16). Subgroup analyses and meta-regression did not affect the findings. CONCLUSION: Results presented in this meta-analysis show that risk of premature death in BD is not only due to suicide and unnatural causes, but somatic comorbidities are also implicated. Not only the prevention of suicide, but also the promotion of physical health and the prevention of physical conditions in individuals with BD may mitigate the premature mortality in this population. Notwithstanding this is to our knowledge the largest synthesis of evidence on BD-related mortality, further well-designed studies are still warranted to inform this field.
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spelling pubmed-106115752023-10-29 All-cause and cause-specific mortality among people with bipolar disorder: a large-scale systematic review and meta-analysis Biazus, Taís Boeira Beraldi, Gabriel Henrique Tokeshi, Lucas Rotenberg, Luísa de Siqueira Dragioti, Elena Carvalho, André F. Solmi, Marco Lafer, Beny Mol Psychiatry Systematic Review OBJECTIVE: Bipolar disorder (BD) is associated with premature mortality. All-cause and specific mortality risks in this population remain unclear, and more studies are still needed to further understand this issue and guide individual and public strategies to prevent mortality in bipolar disorder Thus, a systematic review and meta‐analysis of studies assessing mortality risk in people with BD versus the general population was conducted. The primary outcome was all‐cause mortality, whilst secondary outcomes were mortality due to suicide, natural, unnatural, and specific‐causes mortality. RESULTS: Fifty-seven studies were included (BD; n = 678,353). All‐cause mortality was increased in people with BD (RR = 2.02, 95% CI: 1.89–2.16, k = 39). Specific‐cause mortality was highest for suicide (RR = 11.69, 95% CI: 9.22–14.81, k = 25). Risk of death due to unnatural causes (RR = 7.29, 95% CI: 6.41–8.28, k = 17) and natural causes (RR = 1.90, 95% CI: 1.75–2.06, k = 17) were also increased. Among specific natural causes analyzed, infectious causes had the higher RR (RR = 4,38, 95%CI: 1.5–12.69, k = 3), but the analysis was limited by the inclusion of few studies. Mortality risk due to respiratory (RR = 3.18, 95% CI: 2.55–3.96, k = 6), cardiovascular (RR = 1.76, 95% CI: 1.53–2.01, k = 27), and cerebrovascular (RR = 1.57, 95% CI: 1.34–1.84, k = 13) causes were increased as well. No difference was identified in mortality by cancer (RR = 0.99, 95% CI: 0.88–1.11, k = 16). Subgroup analyses and meta-regression did not affect the findings. CONCLUSION: Results presented in this meta-analysis show that risk of premature death in BD is not only due to suicide and unnatural causes, but somatic comorbidities are also implicated. Not only the prevention of suicide, but also the promotion of physical health and the prevention of physical conditions in individuals with BD may mitigate the premature mortality in this population. Notwithstanding this is to our knowledge the largest synthesis of evidence on BD-related mortality, further well-designed studies are still warranted to inform this field. Nature Publishing Group UK 2023-07-25 2023 /pmc/articles/PMC10611575/ /pubmed/37491460 http://dx.doi.org/10.1038/s41380-023-02109-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Systematic Review
Biazus, Taís Boeira
Beraldi, Gabriel Henrique
Tokeshi, Lucas
Rotenberg, Luísa de Siqueira
Dragioti, Elena
Carvalho, André F.
Solmi, Marco
Lafer, Beny
All-cause and cause-specific mortality among people with bipolar disorder: a large-scale systematic review and meta-analysis
title All-cause and cause-specific mortality among people with bipolar disorder: a large-scale systematic review and meta-analysis
title_full All-cause and cause-specific mortality among people with bipolar disorder: a large-scale systematic review and meta-analysis
title_fullStr All-cause and cause-specific mortality among people with bipolar disorder: a large-scale systematic review and meta-analysis
title_full_unstemmed All-cause and cause-specific mortality among people with bipolar disorder: a large-scale systematic review and meta-analysis
title_short All-cause and cause-specific mortality among people with bipolar disorder: a large-scale systematic review and meta-analysis
title_sort all-cause and cause-specific mortality among people with bipolar disorder: a large-scale systematic review and meta-analysis
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10611575/
https://www.ncbi.nlm.nih.gov/pubmed/37491460
http://dx.doi.org/10.1038/s41380-023-02109-9
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