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Serum IgE in the clinical features and disease outcomes of IgG4-related disease: a large retrospective cohort study

OBJECTIVE: The aim of this study was to investigate the role of serum IgE levels in the clinical features and outcomes of IgG4-related disease (IgG4-RD). METHODS: We retrospectively enrolled 459 newly diagnosed IgG4-RD patients with serum IgE examined at baseline from 2012 to 2019 and compared the c...

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Autores principales: Zhou, Jiaxin, Peng, Yu, Peng, Linyi, Wu, Di, Li, Jing, Jiang, Nan, Li, Jieqiong, Lu, Hui, Liu, Zheng, Luo, Xuan, Teng, Fei, Fei, Yunyun, Zhang, Wen, Zhao, Yan, Zeng, Xiaofeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583198/
https://www.ncbi.nlm.nih.gov/pubmed/33097076
http://dx.doi.org/10.1186/s13075-020-02338-1
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author Zhou, Jiaxin
Peng, Yu
Peng, Linyi
Wu, Di
Li, Jing
Jiang, Nan
Li, Jieqiong
Lu, Hui
Liu, Zheng
Luo, Xuan
Teng, Fei
Fei, Yunyun
Zhang, Wen
Zhao, Yan
Zeng, Xiaofeng
author_facet Zhou, Jiaxin
Peng, Yu
Peng, Linyi
Wu, Di
Li, Jing
Jiang, Nan
Li, Jieqiong
Lu, Hui
Liu, Zheng
Luo, Xuan
Teng, Fei
Fei, Yunyun
Zhang, Wen
Zhao, Yan
Zeng, Xiaofeng
author_sort Zhou, Jiaxin
collection PubMed
description OBJECTIVE: The aim of this study was to investigate the role of serum IgE levels in the clinical features and outcomes of IgG4-related disease (IgG4-RD). METHODS: We retrospectively enrolled 459 newly diagnosed IgG4-RD patients with serum IgE examined at baseline from 2012 to 2019 and compared the clinical features between group A (serum IgE level ≤ 60 KU/L) and group B (serum IgE level > 60 KU/L). Subsequently, 312 patients who had been followed up for ≥ 1 year were further selected to evaluate the correlation between serum IgE level and disease outcome. RESULTS: At baseline, the serum IgE level was positively correlated with the serum IgG4 level (r = 0.1779, P = 0.0001), eosinophil count (r = 0.3004, P < 0.0001), and serum IgG level (r = 0.2189, P < 0.0001) in IgG4-RD patients. Compared with group A, group B had more patients with allergic diseases (P = 0.004), more organ involvement (P = 0.003), and higher IgG4-RD responder index scores (P = 0.002). During follow-up, group A patients had a higher remission induction rate than group B patients (88.4% vs. 73.6%, P = 0.035), while group B patients had a higher relapse rate than group A patients (29.0% vs. 16.2%, P = 0.039). Multivariate analysis found that a serum IgE level > 125 KU/L at baseline was a risk factor for disease relapse (hazard ratio [HR], 1.894 [95% confidence interval (CI) 1.022–3.508]; P = 0.042). Cox regression analysis showed that elevation of the eosinophil count was a risk factor for relapse in both group A and group B patients (HR, 8.504 [95% CI 1.071–42.511]; P = 0.009; and HR, 2.078 [95% CI 1.277–3.380]; P = 0.003, respectively), and the involvement of the lacrimal gland (HR, 1.756 [95% CI 1.108–2.782]; P = 0.017), submandibular gland (HR, 1.654 [95% CI 1.037–2.639]; P = 0.035), and kidney (HR, 3.413 [95% CI 1.076–10.831]; P = 0.037) were also risk factors for relapse in group B patients. CONCLUSION: IgG4-RD patients with high serum IgE levels at baseline were more likely to have higher disease activity, and baseline high IgE levels were associated with disease relapse.
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spelling pubmed-75831982020-10-26 Serum IgE in the clinical features and disease outcomes of IgG4-related disease: a large retrospective cohort study Zhou, Jiaxin Peng, Yu Peng, Linyi Wu, Di Li, Jing Jiang, Nan Li, Jieqiong Lu, Hui Liu, Zheng Luo, Xuan Teng, Fei Fei, Yunyun Zhang, Wen Zhao, Yan Zeng, Xiaofeng Arthritis Res Ther Research Article OBJECTIVE: The aim of this study was to investigate the role of serum IgE levels in the clinical features and outcomes of IgG4-related disease (IgG4-RD). METHODS: We retrospectively enrolled 459 newly diagnosed IgG4-RD patients with serum IgE examined at baseline from 2012 to 2019 and compared the clinical features between group A (serum IgE level ≤ 60 KU/L) and group B (serum IgE level > 60 KU/L). Subsequently, 312 patients who had been followed up for ≥ 1 year were further selected to evaluate the correlation between serum IgE level and disease outcome. RESULTS: At baseline, the serum IgE level was positively correlated with the serum IgG4 level (r = 0.1779, P = 0.0001), eosinophil count (r = 0.3004, P < 0.0001), and serum IgG level (r = 0.2189, P < 0.0001) in IgG4-RD patients. Compared with group A, group B had more patients with allergic diseases (P = 0.004), more organ involvement (P = 0.003), and higher IgG4-RD responder index scores (P = 0.002). During follow-up, group A patients had a higher remission induction rate than group B patients (88.4% vs. 73.6%, P = 0.035), while group B patients had a higher relapse rate than group A patients (29.0% vs. 16.2%, P = 0.039). Multivariate analysis found that a serum IgE level > 125 KU/L at baseline was a risk factor for disease relapse (hazard ratio [HR], 1.894 [95% confidence interval (CI) 1.022–3.508]; P = 0.042). Cox regression analysis showed that elevation of the eosinophil count was a risk factor for relapse in both group A and group B patients (HR, 8.504 [95% CI 1.071–42.511]; P = 0.009; and HR, 2.078 [95% CI 1.277–3.380]; P = 0.003, respectively), and the involvement of the lacrimal gland (HR, 1.756 [95% CI 1.108–2.782]; P = 0.017), submandibular gland (HR, 1.654 [95% CI 1.037–2.639]; P = 0.035), and kidney (HR, 3.413 [95% CI 1.076–10.831]; P = 0.037) were also risk factors for relapse in group B patients. CONCLUSION: IgG4-RD patients with high serum IgE levels at baseline were more likely to have higher disease activity, and baseline high IgE levels were associated with disease relapse. BioMed Central 2020-10-23 2020 /pmc/articles/PMC7583198/ /pubmed/33097076 http://dx.doi.org/10.1186/s13075-020-02338-1 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article
Zhou, Jiaxin
Peng, Yu
Peng, Linyi
Wu, Di
Li, Jing
Jiang, Nan
Li, Jieqiong
Lu, Hui
Liu, Zheng
Luo, Xuan
Teng, Fei
Fei, Yunyun
Zhang, Wen
Zhao, Yan
Zeng, Xiaofeng
Serum IgE in the clinical features and disease outcomes of IgG4-related disease: a large retrospective cohort study
title Serum IgE in the clinical features and disease outcomes of IgG4-related disease: a large retrospective cohort study
title_full Serum IgE in the clinical features and disease outcomes of IgG4-related disease: a large retrospective cohort study
title_fullStr Serum IgE in the clinical features and disease outcomes of IgG4-related disease: a large retrospective cohort study
title_full_unstemmed Serum IgE in the clinical features and disease outcomes of IgG4-related disease: a large retrospective cohort study
title_short Serum IgE in the clinical features and disease outcomes of IgG4-related disease: a large retrospective cohort study
title_sort serum ige in the clinical features and disease outcomes of igg4-related disease: a large retrospective cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583198/
https://www.ncbi.nlm.nih.gov/pubmed/33097076
http://dx.doi.org/10.1186/s13075-020-02338-1
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