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Risk prediction model for mortality in microscopic polyangiitis: multicentre REVEAL cohort study
BACKGROUND: To establish refined risk prediction models for mortality in patients with microscopic polyangiitis (MPA) by using comprehensive clinical characteristics. METHODS: Data from the multicentre Japanese registry of patients with vasculitis (REVEAL cohort) were used in our analysis. In total,...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10658814/ https://www.ncbi.nlm.nih.gov/pubmed/37986108 http://dx.doi.org/10.1186/s13075-023-03210-8 |
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author | Kotani, Takuya Matsuda, Shogo Okazaki, Ayana Nishioka, Daisuke Watanabe, Ryu Gon, Takaho Manabe, Atsushi Shoji, Mikihito Kadoba, Keiichiro Hiwa, Ryosuke Yamamoto, Wataru Hashimoto, Motomu Takeuchi, Tohru |
author_facet | Kotani, Takuya Matsuda, Shogo Okazaki, Ayana Nishioka, Daisuke Watanabe, Ryu Gon, Takaho Manabe, Atsushi Shoji, Mikihito Kadoba, Keiichiro Hiwa, Ryosuke Yamamoto, Wataru Hashimoto, Motomu Takeuchi, Tohru |
author_sort | Kotani, Takuya |
collection | PubMed |
description | BACKGROUND: To establish refined risk prediction models for mortality in patients with microscopic polyangiitis (MPA) by using comprehensive clinical characteristics. METHODS: Data from the multicentre Japanese registry of patients with vasculitis (REVEAL cohort) were used in our analysis. In total, 194 patients with newly diagnosed MPA were included, and baseline demographic, clinical, laboratory, and treatment details were collected. Univariate and multivariate analyses were conducted to identify the significant risk factors predictive of mortality. RESULTS: Over a median follow-up of 202.5 (84–352) weeks, 60 (30.9%) of 194 patients died. The causes of death included MPA-related vasculitis (18.3%), infection (50.0%), and others (31.7%). Deceased patients were older (median age 76.2 years) than survivors (72.3 years) (P < 0.0001). The death group had shorter observation periods (median 128.5 [35.3–248] weeks) than the survivor group (229 [112–392] weeks). Compared to survivors, the death group exhibited a higher smoking index, lower serum albumin levels, higher serum C-reactive protein levels, higher Birmingham Vasculitis Activity Score (BVAS), higher Five-Factor Score, and a more severe European Vasculitis Study Group (EUVAS) categorization system. Multivariate analysis revealed that higher BVAS and severe EUVAS independently predicted mortality. Kaplan–Meier survival curves demonstrated lower survival rates for BVAS ≥20 and severe EUVAS, and a risk prediction model (RPM) based on these stratified patients into low, moderate, and high-risk mortality groups. CONCLUSIONS: The developed RPM is promising to predict mortality in patients with MPA and provides clinicians with a valuable tool for risk assessment and informed clinical decision-making. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-023-03210-8. |
format | Online Article Text |
id | pubmed-10658814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106588142023-11-20 Risk prediction model for mortality in microscopic polyangiitis: multicentre REVEAL cohort study Kotani, Takuya Matsuda, Shogo Okazaki, Ayana Nishioka, Daisuke Watanabe, Ryu Gon, Takaho Manabe, Atsushi Shoji, Mikihito Kadoba, Keiichiro Hiwa, Ryosuke Yamamoto, Wataru Hashimoto, Motomu Takeuchi, Tohru Arthritis Res Ther Research BACKGROUND: To establish refined risk prediction models for mortality in patients with microscopic polyangiitis (MPA) by using comprehensive clinical characteristics. METHODS: Data from the multicentre Japanese registry of patients with vasculitis (REVEAL cohort) were used in our analysis. In total, 194 patients with newly diagnosed MPA were included, and baseline demographic, clinical, laboratory, and treatment details were collected. Univariate and multivariate analyses were conducted to identify the significant risk factors predictive of mortality. RESULTS: Over a median follow-up of 202.5 (84–352) weeks, 60 (30.9%) of 194 patients died. The causes of death included MPA-related vasculitis (18.3%), infection (50.0%), and others (31.7%). Deceased patients were older (median age 76.2 years) than survivors (72.3 years) (P < 0.0001). The death group had shorter observation periods (median 128.5 [35.3–248] weeks) than the survivor group (229 [112–392] weeks). Compared to survivors, the death group exhibited a higher smoking index, lower serum albumin levels, higher serum C-reactive protein levels, higher Birmingham Vasculitis Activity Score (BVAS), higher Five-Factor Score, and a more severe European Vasculitis Study Group (EUVAS) categorization system. Multivariate analysis revealed that higher BVAS and severe EUVAS independently predicted mortality. Kaplan–Meier survival curves demonstrated lower survival rates for BVAS ≥20 and severe EUVAS, and a risk prediction model (RPM) based on these stratified patients into low, moderate, and high-risk mortality groups. CONCLUSIONS: The developed RPM is promising to predict mortality in patients with MPA and provides clinicians with a valuable tool for risk assessment and informed clinical decision-making. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13075-023-03210-8. BioMed Central 2023-11-20 2023 /pmc/articles/PMC10658814/ /pubmed/37986108 http://dx.doi.org/10.1186/s13075-023-03210-8 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Kotani, Takuya Matsuda, Shogo Okazaki, Ayana Nishioka, Daisuke Watanabe, Ryu Gon, Takaho Manabe, Atsushi Shoji, Mikihito Kadoba, Keiichiro Hiwa, Ryosuke Yamamoto, Wataru Hashimoto, Motomu Takeuchi, Tohru Risk prediction model for mortality in microscopic polyangiitis: multicentre REVEAL cohort study |
title | Risk prediction model for mortality in microscopic polyangiitis: multicentre REVEAL cohort study |
title_full | Risk prediction model for mortality in microscopic polyangiitis: multicentre REVEAL cohort study |
title_fullStr | Risk prediction model for mortality in microscopic polyangiitis: multicentre REVEAL cohort study |
title_full_unstemmed | Risk prediction model for mortality in microscopic polyangiitis: multicentre REVEAL cohort study |
title_short | Risk prediction model for mortality in microscopic polyangiitis: multicentre REVEAL cohort study |
title_sort | risk prediction model for mortality in microscopic polyangiitis: multicentre reveal cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10658814/ https://www.ncbi.nlm.nih.gov/pubmed/37986108 http://dx.doi.org/10.1186/s13075-023-03210-8 |
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