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Serum level of IFNβ distinguishes early from late relapses after biologics withdrawal in rheumatoid arthritis
Since the advent of biological disease modifying anti-rheumatic drugs (bDMARDs) in the treatment of rheumatoid arthritis (RA), most RA patients receiving such drugs have achieved remission at the expense of cost and infection risk. After bDMARDs are withdrawn, a substantial proportion of patients wo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529916/ https://www.ncbi.nlm.nih.gov/pubmed/36192530 http://dx.doi.org/10.1038/s41598-022-21160-0 |
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author | Sakashita, Eiji Nagatani, Katsuya Endo, Hitoshi Minota, Seiji |
author_facet | Sakashita, Eiji Nagatani, Katsuya Endo, Hitoshi Minota, Seiji |
author_sort | Sakashita, Eiji |
collection | PubMed |
description | Since the advent of biological disease modifying anti-rheumatic drugs (bDMARDs) in the treatment of rheumatoid arthritis (RA), most RA patients receiving such drugs have achieved remission at the expense of cost and infection risk. After bDMARDs are withdrawn, a substantial proportion of patients would have relapses even if they were in complete remission. In our previous report, relapse prediction could be made at the time of bDMARD withdrawal by measuring the serum levels of five cytokines. We report herein that, among 73 cytokines examined, serum levels of only interferon β (IFNβ) at the time of bDMARD withdrawal could predict early relapse (within 5 months) in patients who were categorized to relapse by the five cytokines in our previous report, with a cut-off value of 3.38 in log(2) and AUC of 0.833. High serum levels of IFNβ in the early-relapse group remained high until actual relapse occurred. Therefore, patients who relapse early might be biochemically different from those who relapse late or do not relapse at all. We recommend that patients who are predicted to relapse early continue bDMARDs even if they are in complete remission. This finding contributes to shared decision-making regarding how and when bDMARDs should be discontinued. |
format | Online Article Text |
id | pubmed-9529916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95299162022-10-05 Serum level of IFNβ distinguishes early from late relapses after biologics withdrawal in rheumatoid arthritis Sakashita, Eiji Nagatani, Katsuya Endo, Hitoshi Minota, Seiji Sci Rep Article Since the advent of biological disease modifying anti-rheumatic drugs (bDMARDs) in the treatment of rheumatoid arthritis (RA), most RA patients receiving such drugs have achieved remission at the expense of cost and infection risk. After bDMARDs are withdrawn, a substantial proportion of patients would have relapses even if they were in complete remission. In our previous report, relapse prediction could be made at the time of bDMARD withdrawal by measuring the serum levels of five cytokines. We report herein that, among 73 cytokines examined, serum levels of only interferon β (IFNβ) at the time of bDMARD withdrawal could predict early relapse (within 5 months) in patients who were categorized to relapse by the five cytokines in our previous report, with a cut-off value of 3.38 in log(2) and AUC of 0.833. High serum levels of IFNβ in the early-relapse group remained high until actual relapse occurred. Therefore, patients who relapse early might be biochemically different from those who relapse late or do not relapse at all. We recommend that patients who are predicted to relapse early continue bDMARDs even if they are in complete remission. This finding contributes to shared decision-making regarding how and when bDMARDs should be discontinued. Nature Publishing Group UK 2022-10-03 /pmc/articles/PMC9529916/ /pubmed/36192530 http://dx.doi.org/10.1038/s41598-022-21160-0 Text en © The Author(s) 2022 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/) . |
spellingShingle | Article Sakashita, Eiji Nagatani, Katsuya Endo, Hitoshi Minota, Seiji Serum level of IFNβ distinguishes early from late relapses after biologics withdrawal in rheumatoid arthritis |
title | Serum level of IFNβ distinguishes early from late relapses after biologics withdrawal in rheumatoid arthritis |
title_full | Serum level of IFNβ distinguishes early from late relapses after biologics withdrawal in rheumatoid arthritis |
title_fullStr | Serum level of IFNβ distinguishes early from late relapses after biologics withdrawal in rheumatoid arthritis |
title_full_unstemmed | Serum level of IFNβ distinguishes early from late relapses after biologics withdrawal in rheumatoid arthritis |
title_short | Serum level of IFNβ distinguishes early from late relapses after biologics withdrawal in rheumatoid arthritis |
title_sort | serum level of ifnβ distinguishes early from late relapses after biologics withdrawal in rheumatoid arthritis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529916/ https://www.ncbi.nlm.nih.gov/pubmed/36192530 http://dx.doi.org/10.1038/s41598-022-21160-0 |
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