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Rituximab Therapy in Renal Amyloidosis Secondary to Rheumatoid Arthritis

Secondary amyloid A (AA) amyloidosis is a late and serious complication of poorly controlled, chronic inflammatory diseases. Rheumatoid arthritis (RA) patients with poorly controlled, longstanding disease and those with extra-articular manifestations are under risk for the development of AA amyloido...

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Autores principales: Kilic, Levent, Erden, Abdulsamet, Sener, Yusuf Ziya, Armagan, Berkan, Sari, Alper, Kalyoncu, Umut, Karadag, Omer, Akdogan, Ali, Dogan, Ismail, Apras Bilgen, Sule, Kiraz, Sedat, Ertenli, Ihsan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316109/
https://www.ncbi.nlm.nih.gov/pubmed/30400666
http://dx.doi.org/10.3390/biom8040136
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author Kilic, Levent
Erden, Abdulsamet
Sener, Yusuf Ziya
Armagan, Berkan
Sari, Alper
Kalyoncu, Umut
Karadag, Omer
Akdogan, Ali
Dogan, Ismail
Apras Bilgen, Sule
Kiraz, Sedat
Ertenli, Ihsan
author_facet Kilic, Levent
Erden, Abdulsamet
Sener, Yusuf Ziya
Armagan, Berkan
Sari, Alper
Kalyoncu, Umut
Karadag, Omer
Akdogan, Ali
Dogan, Ismail
Apras Bilgen, Sule
Kiraz, Sedat
Ertenli, Ihsan
author_sort Kilic, Levent
collection PubMed
description Secondary amyloid A (AA) amyloidosis is a late and serious complication of poorly controlled, chronic inflammatory diseases. Rheumatoid arthritis (RA) patients with poorly controlled, longstanding disease and those with extra-articular manifestations are under risk for the development of AA amyloidosis. Although new drugs have proven to be significantly effective in the treatment of secondary AA amyloidosis, no treatment modality has proven to be ideal. To date, only in small case series preliminary clinical improvement have been shown with rituximab therapy for AA amyloidosis secondary to RA that is refractory to TNF-α inhibitors (TNF-i) therapy. In these case series, we assessed the efficacy and safety of rituximab therapy for patients with RA and secondary amyloidosis. Hacettepe University Biologic Registry was developed at 2005. The data of the RA patients who were prescribed a biological drug were recorded regularly. Patients with biopsy proven AA amyloidosis patients were screened. Of 1022 RA patients under biologic therapy, 0.7% patients had clinically apparent histologically confirmed amyloidosis. Four of seven patients who were prescribed rituximab at least one infusion enrolled to those case series. Two of four patients showed significant clinical improvement and one of them also had decrease in proteinuria and the other one had stable renal function and proteinuria. The main goal for the treatment of AA amyloidosis is to control the activity of the underlying disorder. In this study, we showed that rituximab may be an effective treatment in RA patients with amyloidosis who were unresponsive to conventional disease modifying anti-rheumatic drugs (DMARDs) and/or TNFi.
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spelling pubmed-63161092019-01-10 Rituximab Therapy in Renal Amyloidosis Secondary to Rheumatoid Arthritis Kilic, Levent Erden, Abdulsamet Sener, Yusuf Ziya Armagan, Berkan Sari, Alper Kalyoncu, Umut Karadag, Omer Akdogan, Ali Dogan, Ismail Apras Bilgen, Sule Kiraz, Sedat Ertenli, Ihsan Biomolecules Article Secondary amyloid A (AA) amyloidosis is a late and serious complication of poorly controlled, chronic inflammatory diseases. Rheumatoid arthritis (RA) patients with poorly controlled, longstanding disease and those with extra-articular manifestations are under risk for the development of AA amyloidosis. Although new drugs have proven to be significantly effective in the treatment of secondary AA amyloidosis, no treatment modality has proven to be ideal. To date, only in small case series preliminary clinical improvement have been shown with rituximab therapy for AA amyloidosis secondary to RA that is refractory to TNF-α inhibitors (TNF-i) therapy. In these case series, we assessed the efficacy and safety of rituximab therapy for patients with RA and secondary amyloidosis. Hacettepe University Biologic Registry was developed at 2005. The data of the RA patients who were prescribed a biological drug were recorded regularly. Patients with biopsy proven AA amyloidosis patients were screened. Of 1022 RA patients under biologic therapy, 0.7% patients had clinically apparent histologically confirmed amyloidosis. Four of seven patients who were prescribed rituximab at least one infusion enrolled to those case series. Two of four patients showed significant clinical improvement and one of them also had decrease in proteinuria and the other one had stable renal function and proteinuria. The main goal for the treatment of AA amyloidosis is to control the activity of the underlying disorder. In this study, we showed that rituximab may be an effective treatment in RA patients with amyloidosis who were unresponsive to conventional disease modifying anti-rheumatic drugs (DMARDs) and/or TNFi. MDPI 2018-11-05 /pmc/articles/PMC6316109/ /pubmed/30400666 http://dx.doi.org/10.3390/biom8040136 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kilic, Levent
Erden, Abdulsamet
Sener, Yusuf Ziya
Armagan, Berkan
Sari, Alper
Kalyoncu, Umut
Karadag, Omer
Akdogan, Ali
Dogan, Ismail
Apras Bilgen, Sule
Kiraz, Sedat
Ertenli, Ihsan
Rituximab Therapy in Renal Amyloidosis Secondary to Rheumatoid Arthritis
title Rituximab Therapy in Renal Amyloidosis Secondary to Rheumatoid Arthritis
title_full Rituximab Therapy in Renal Amyloidosis Secondary to Rheumatoid Arthritis
title_fullStr Rituximab Therapy in Renal Amyloidosis Secondary to Rheumatoid Arthritis
title_full_unstemmed Rituximab Therapy in Renal Amyloidosis Secondary to Rheumatoid Arthritis
title_short Rituximab Therapy in Renal Amyloidosis Secondary to Rheumatoid Arthritis
title_sort rituximab therapy in renal amyloidosis secondary to rheumatoid arthritis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316109/
https://www.ncbi.nlm.nih.gov/pubmed/30400666
http://dx.doi.org/10.3390/biom8040136
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