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The risk of organ-based comorbidities in psoriasis: a systematic review and meta-analysis()

BACKGROUND: The close relationship between psoriasis and concomitant diseases is widely accepted. However, a comprehensive analysis of organ-based comorbidities in psoriasis is still lacking. OBJECTIVE: The authors aimed to present the risk of organ-based comorbidities in psoriasis by comparing the...

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Autores principales: Tang, Xuemei, Chen, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453528/
https://www.ncbi.nlm.nih.gov/pubmed/35850940
http://dx.doi.org/10.1016/j.abd.2021.10.007
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author Tang, Xuemei
Chen, Ling
author_facet Tang, Xuemei
Chen, Ling
author_sort Tang, Xuemei
collection PubMed
description BACKGROUND: The close relationship between psoriasis and concomitant diseases is widely accepted. However, a comprehensive analysis of organ-based comorbidities in psoriasis is still lacking. OBJECTIVE: The authors aimed to present the risk of organ-based comorbidities in psoriasis by comparing the general population. METHODS: The authors retrieved a search of Pubmed, EMBASE, and Cochrane databases for studies reporting organ-based comorbidities in psoriasis versus the general population. Observational studies that met the following criteria were assessed: 1) Psoriasis diagnosis; 2) Cardiovascular or kidney or liver or respiratory or cerebrovascular outcomes; 3) Comparison group of individuals without psoriasis. Pooled Relative Risks (pRRs) and 95% Confidence Intervals (CIs) were calculated by using the random-effect model. RESULTS: Fifteen observational studies with 216,348 psoriatic patients and 9,896,962 individuals from the general population were included. Psoriasis showed a greater risk of organ-based comorbidities. Compared to the general population, pRR for all organ-based comorbidities was 1.20 (95% CI 1.11‒1.31) in psoriasis, and pRR was lower in mild 0.61 (95% CI 0.46‒0.81) than in moderate/severe patients. pRR was 1.20 (95% CI 1.11‒1.30) for cardiovascular, 1.56 (95% CI 1.20‒2.04), and 1.75 (95% CI 1.33‒2.29) for cerebrovascular and liver diseases, respectively. pRR for coexisting renal and cardiovascular events was 1.09 (95% CI 1.01‒1.18). pRR for coexisting renal and cerebrovascular events was 1.28 (95% CI 0.99‒1.66). pRR for coexisting renal and liver diseases was 1.46 (95% CI 1.10‒1.94). pRR for coexisting cardiovascular and liver diseases was 1.41 (95% CI 1.11‒1.80). STUDY LIMITATIONS: There is heterogeneity. CONCLUSION: Psoriasis has a higher risk of single and multiple organ-based comorbidities than the general population. The present study will further improve attention to psoriasis as a systemic inflammatory disease.
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spelling pubmed-94535282022-09-10 The risk of organ-based comorbidities in psoriasis: a systematic review and meta-analysis() Tang, Xuemei Chen, Ling An Bras Dermatol Original Article BACKGROUND: The close relationship between psoriasis and concomitant diseases is widely accepted. However, a comprehensive analysis of organ-based comorbidities in psoriasis is still lacking. OBJECTIVE: The authors aimed to present the risk of organ-based comorbidities in psoriasis by comparing the general population. METHODS: The authors retrieved a search of Pubmed, EMBASE, and Cochrane databases for studies reporting organ-based comorbidities in psoriasis versus the general population. Observational studies that met the following criteria were assessed: 1) Psoriasis diagnosis; 2) Cardiovascular or kidney or liver or respiratory or cerebrovascular outcomes; 3) Comparison group of individuals without psoriasis. Pooled Relative Risks (pRRs) and 95% Confidence Intervals (CIs) were calculated by using the random-effect model. RESULTS: Fifteen observational studies with 216,348 psoriatic patients and 9,896,962 individuals from the general population were included. Psoriasis showed a greater risk of organ-based comorbidities. Compared to the general population, pRR for all organ-based comorbidities was 1.20 (95% CI 1.11‒1.31) in psoriasis, and pRR was lower in mild 0.61 (95% CI 0.46‒0.81) than in moderate/severe patients. pRR was 1.20 (95% CI 1.11‒1.30) for cardiovascular, 1.56 (95% CI 1.20‒2.04), and 1.75 (95% CI 1.33‒2.29) for cerebrovascular and liver diseases, respectively. pRR for coexisting renal and cardiovascular events was 1.09 (95% CI 1.01‒1.18). pRR for coexisting renal and cerebrovascular events was 1.28 (95% CI 0.99‒1.66). pRR for coexisting renal and liver diseases was 1.46 (95% CI 1.10‒1.94). pRR for coexisting cardiovascular and liver diseases was 1.41 (95% CI 1.11‒1.80). STUDY LIMITATIONS: There is heterogeneity. CONCLUSION: Psoriasis has a higher risk of single and multiple organ-based comorbidities than the general population. The present study will further improve attention to psoriasis as a systemic inflammatory disease. Sociedade Brasileira de Dermatologia 2022 2022-07-15 /pmc/articles/PMC9453528/ /pubmed/35850940 http://dx.doi.org/10.1016/j.abd.2021.10.007 Text en © 2022 Sociedade Brasileira de Dermatologia. Published by Elsevier España, S.L.U. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Article
Tang, Xuemei
Chen, Ling
The risk of organ-based comorbidities in psoriasis: a systematic review and meta-analysis()
title The risk of organ-based comorbidities in psoriasis: a systematic review and meta-analysis()
title_full The risk of organ-based comorbidities in psoriasis: a systematic review and meta-analysis()
title_fullStr The risk of organ-based comorbidities in psoriasis: a systematic review and meta-analysis()
title_full_unstemmed The risk of organ-based comorbidities in psoriasis: a systematic review and meta-analysis()
title_short The risk of organ-based comorbidities in psoriasis: a systematic review and meta-analysis()
title_sort risk of organ-based comorbidities in psoriasis: a systematic review and meta-analysis()
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9453528/
https://www.ncbi.nlm.nih.gov/pubmed/35850940
http://dx.doi.org/10.1016/j.abd.2021.10.007
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