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Serum IgG4 level during initial treatment as a predictor of relapse in IgG4-related disease

INTRODUCTION: We aimed to investigate the predictors of relapse in immunoglobulin G4-related disease (IgG4-RD), focusing on the serum IgG4 levels during initial treatment. METHODS: We retrospectively recruited 57 patients with IgG4-RD who were treated with immunosuppressants and elevated serum IgG4...

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Autores principales: Choi, Su Jin, Ahn, Soo Min, Oh, Ji Seon, Hong, Seokchan, Lee, Chang-Keun, Yoo, Bin, Kim, Yong-Gil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9997947/
https://www.ncbi.nlm.nih.gov/pubmed/36893163
http://dx.doi.org/10.1371/journal.pone.0282852
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author Choi, Su Jin
Ahn, Soo Min
Oh, Ji Seon
Hong, Seokchan
Lee, Chang-Keun
Yoo, Bin
Kim, Yong-Gil
author_facet Choi, Su Jin
Ahn, Soo Min
Oh, Ji Seon
Hong, Seokchan
Lee, Chang-Keun
Yoo, Bin
Kim, Yong-Gil
author_sort Choi, Su Jin
collection PubMed
description INTRODUCTION: We aimed to investigate the predictors of relapse in immunoglobulin G4-related disease (IgG4-RD), focusing on the serum IgG4 levels during initial treatment. METHODS: We retrospectively recruited 57 patients with IgG4-RD who were treated with immunosuppressants and elevated serum IgG4 levels in a tertiary hospital between January 2011 and December 2020. They were followed up for ≥ 6 months after initiation of immunosuppressive therapy. Clinical and laboratory findings including serum IgG4 levels (reference value: 6–121 mg/dL) were compared between relapsed (n = 13) and non-relapsed (n = 44) groups. Multivariate Cox regression analysis was used to assess the predictors for relapse. We performed a Kaplan–Meier analysis with a log-rank test to evaluate the cumulative relapse rate for two years. RESULTS: Median serum IgG4 levels at baseline were 321 mg/dL in the relapsed group and 299 mg/dL in the non-relapsed group. Serum IgG4 levels were normalized after six months in five (38.5%) relapsed and 28 (63.6%) non-relapsed patients. In multivariate Cox regression analysis, the normalization of serum IgG4 levels at six months was associated with a lower risk of relapse, with a hazard ratio of 0.232 (p = 0.019). Central nervous system involvement was associated with the relapse, with a hazard ratio of 21.130 (p = 0.015). The cumulative relapse rate for two years was lower in the normal serum IgG4 group at six months than in the elevated serum IgG4 group at six months (p = 0.027). CONCLUSION: Our study suggests that normalization of serum IgG4 levels during immunosuppressive treatment for IgG4-RD independently predicts relapse-free outcomes. Thus, monitoring serum IgG4 levels might be used as a marker of prognosis.
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spelling pubmed-99979472023-03-10 Serum IgG4 level during initial treatment as a predictor of relapse in IgG4-related disease Choi, Su Jin Ahn, Soo Min Oh, Ji Seon Hong, Seokchan Lee, Chang-Keun Yoo, Bin Kim, Yong-Gil PLoS One Research Article INTRODUCTION: We aimed to investigate the predictors of relapse in immunoglobulin G4-related disease (IgG4-RD), focusing on the serum IgG4 levels during initial treatment. METHODS: We retrospectively recruited 57 patients with IgG4-RD who were treated with immunosuppressants and elevated serum IgG4 levels in a tertiary hospital between January 2011 and December 2020. They were followed up for ≥ 6 months after initiation of immunosuppressive therapy. Clinical and laboratory findings including serum IgG4 levels (reference value: 6–121 mg/dL) were compared between relapsed (n = 13) and non-relapsed (n = 44) groups. Multivariate Cox regression analysis was used to assess the predictors for relapse. We performed a Kaplan–Meier analysis with a log-rank test to evaluate the cumulative relapse rate for two years. RESULTS: Median serum IgG4 levels at baseline were 321 mg/dL in the relapsed group and 299 mg/dL in the non-relapsed group. Serum IgG4 levels were normalized after six months in five (38.5%) relapsed and 28 (63.6%) non-relapsed patients. In multivariate Cox regression analysis, the normalization of serum IgG4 levels at six months was associated with a lower risk of relapse, with a hazard ratio of 0.232 (p = 0.019). Central nervous system involvement was associated with the relapse, with a hazard ratio of 21.130 (p = 0.015). The cumulative relapse rate for two years was lower in the normal serum IgG4 group at six months than in the elevated serum IgG4 group at six months (p = 0.027). CONCLUSION: Our study suggests that normalization of serum IgG4 levels during immunosuppressive treatment for IgG4-RD independently predicts relapse-free outcomes. Thus, monitoring serum IgG4 levels might be used as a marker of prognosis. Public Library of Science 2023-03-09 /pmc/articles/PMC9997947/ /pubmed/36893163 http://dx.doi.org/10.1371/journal.pone.0282852 Text en © 2023 Choi et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Choi, Su Jin
Ahn, Soo Min
Oh, Ji Seon
Hong, Seokchan
Lee, Chang-Keun
Yoo, Bin
Kim, Yong-Gil
Serum IgG4 level during initial treatment as a predictor of relapse in IgG4-related disease
title Serum IgG4 level during initial treatment as a predictor of relapse in IgG4-related disease
title_full Serum IgG4 level during initial treatment as a predictor of relapse in IgG4-related disease
title_fullStr Serum IgG4 level during initial treatment as a predictor of relapse in IgG4-related disease
title_full_unstemmed Serum IgG4 level during initial treatment as a predictor of relapse in IgG4-related disease
title_short Serum IgG4 level during initial treatment as a predictor of relapse in IgG4-related disease
title_sort serum igg4 level during initial treatment as a predictor of relapse in igg4-related disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9997947/
https://www.ncbi.nlm.nih.gov/pubmed/36893163
http://dx.doi.org/10.1371/journal.pone.0282852
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