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Comorbidities in psoriatic arthritis: a systematic review and meta-analysis

The aims of this systematic review and meta-analysis were to: (1) describe the prevalence of commonly reported comorbidities in psoriatic arthritis (PsA), (2) compare the incidence and/or prevalence of comorbidities between PsA and control populations; and (3) examine the impact of comorbidities on...

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Autores principales: Gupta, Sonal, Syrimi, Zoe, Hughes, David M., Zhao, Sizheng Steven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835184/
https://www.ncbi.nlm.nih.gov/pubmed/33423070
http://dx.doi.org/10.1007/s00296-020-04775-2
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author Gupta, Sonal
Syrimi, Zoe
Hughes, David M.
Zhao, Sizheng Steven
author_facet Gupta, Sonal
Syrimi, Zoe
Hughes, David M.
Zhao, Sizheng Steven
author_sort Gupta, Sonal
collection PubMed
description The aims of this systematic review and meta-analysis were to: (1) describe the prevalence of commonly reported comorbidities in psoriatic arthritis (PsA), (2) compare the incidence and/or prevalence of comorbidities between PsA and control populations; and (3) examine the impact of comorbidities on PsA outcomes. We systematically searched Medline, PubMed, Scopus, and Web of Science using a predefined protocol in accordance with PRISMA guidelines. Studies reporting only one comorbidity, or a few closely related diseases within one organ system, were excluded. Where possible, meta-analysis was performed using random-effects models. We included 39 studies amounting to over 152 thousand PsA patients. We performed meta-analysis for the prevalence of 21 commonly reported comorbidities. The most prevalent comorbidities were hypertension (pooled prevalence 34%), metabolic syndrome (29%), obesity (27%), hyperlipidaemia (24%) and any cardiovascular diseases (19%). Eleven studies consistently showed higher prevalence of comorbidities in PsA than controls. Five studies showed that comorbid patients had more severe disease, poorer quality of life, and increased discontinuation of treatment. Comorbidities, particularly cardiometabolic disorders, were highly prevalent in PsA and more common than in healthy controls. Comorbidities were associated with adverse disease features, but more research is needed on their impact on longitudinal outcomes such as treatment response, work productivity and mortality. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00296-020-04775-2.
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spelling pubmed-78351842021-01-29 Comorbidities in psoriatic arthritis: a systematic review and meta-analysis Gupta, Sonal Syrimi, Zoe Hughes, David M. Zhao, Sizheng Steven Rheumatol Int Systematic Review The aims of this systematic review and meta-analysis were to: (1) describe the prevalence of commonly reported comorbidities in psoriatic arthritis (PsA), (2) compare the incidence and/or prevalence of comorbidities between PsA and control populations; and (3) examine the impact of comorbidities on PsA outcomes. We systematically searched Medline, PubMed, Scopus, and Web of Science using a predefined protocol in accordance with PRISMA guidelines. Studies reporting only one comorbidity, or a few closely related diseases within one organ system, were excluded. Where possible, meta-analysis was performed using random-effects models. We included 39 studies amounting to over 152 thousand PsA patients. We performed meta-analysis for the prevalence of 21 commonly reported comorbidities. The most prevalent comorbidities were hypertension (pooled prevalence 34%), metabolic syndrome (29%), obesity (27%), hyperlipidaemia (24%) and any cardiovascular diseases (19%). Eleven studies consistently showed higher prevalence of comorbidities in PsA than controls. Five studies showed that comorbid patients had more severe disease, poorer quality of life, and increased discontinuation of treatment. Comorbidities, particularly cardiometabolic disorders, were highly prevalent in PsA and more common than in healthy controls. Comorbidities were associated with adverse disease features, but more research is needed on their impact on longitudinal outcomes such as treatment response, work productivity and mortality. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00296-020-04775-2. Springer Berlin Heidelberg 2021-01-09 2021 /pmc/articles/PMC7835184/ /pubmed/33423070 http://dx.doi.org/10.1007/s00296-020-04775-2 Text en © The Author(s) 2021 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/.
spellingShingle Systematic Review
Gupta, Sonal
Syrimi, Zoe
Hughes, David M.
Zhao, Sizheng Steven
Comorbidities in psoriatic arthritis: a systematic review and meta-analysis
title Comorbidities in psoriatic arthritis: a systematic review and meta-analysis
title_full Comorbidities in psoriatic arthritis: a systematic review and meta-analysis
title_fullStr Comorbidities in psoriatic arthritis: a systematic review and meta-analysis
title_full_unstemmed Comorbidities in psoriatic arthritis: a systematic review and meta-analysis
title_short Comorbidities in psoriatic arthritis: a systematic review and meta-analysis
title_sort comorbidities in psoriatic arthritis: a systematic review and meta-analysis
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835184/
https://www.ncbi.nlm.nih.gov/pubmed/33423070
http://dx.doi.org/10.1007/s00296-020-04775-2
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