Case Report

J Rheum Dis 2013; 20(6): 361-363

Published online December 30, 2013

© Korean College of Rheumatology

A Case of Etanercept Treatment in a Patient with Ankylosing Spondylitis on Peritoneal Dialysis

Sang-A Choi1, Seung-Geun Lee1, Sang-Heon Song1, Ji-Min Kim1, Hye-Yoon Jang1, Woo-Jin Jung1, Jong-Hyun Choi1, Young-Eun Park2, Seong-Hu Park3, Joung-Wook Lee4, Jun-Hee Lee5, Seung-Hoon Baek5, Geun-Tae Kim6

Department of Internal Medicine, Pusan National University School of Medicine1, Busan, Malgeunsem Hospital2, Changwon, Young-do Hospital3, Busan St. Mary’s Medical Center4, Division of Rheumatology, Department of Internal Medicine, Ilsin Christian Hospital5, Division of Rheumatology, Department of Internal Medicine, Kosin University College of Medicine6, Busan, Korea

Correspondence to : Seung-Hoon Baek

Received: October 17, 2012; Accepted: November 7, 2012

Abstract

Treatments for patient with ankylosing spondylitis (AS) include non-steroidal anti-inflammatory drugs (NSAIDs), disease-modifying antirheumatic drugs (DMARDs) and anti-tumor necrosis factor-alpha (TNFα) agents. However, owing to the well-known nephrotoxicity of NSAIDs and some DMARDs, the use of these drugs is limited in AS patients with renal insufficiency. As the pharmacokinetics and metabolism of anti-TNFα agents in patients of end stage renal disease, especially those receiving peritoneal dialysis (PD), have not been investigated well, little is known about treating them with anti-TNFα agents. We described the safety and efficacy of etanercept, a soluble fusion protein comprising the TNF receptor 2 in linkage with the Fc portion of immunoglobulin G, in a 40-year-old male AS patient receiving PD.

Keywords Ankylosing spondylitis, End-stage renal disease, Peritoneal dialysis, Tumor necrosis factor-alpha

Article

Case Report

J Rheum Dis 2013; 20(6): 361-363

Published online December 30, 2013

Copyright © Korean College of Rheumatology.

A Case of Etanercept Treatment in a Patient with Ankylosing Spondylitis on Peritoneal Dialysis

Sang-A Choi1, Seung-Geun Lee1, Sang-Heon Song1, Ji-Min Kim1, Hye-Yoon Jang1, Woo-Jin Jung1, Jong-Hyun Choi1, Young-Eun Park2, Seong-Hu Park3, Joung-Wook Lee4, Jun-Hee Lee5, Seung-Hoon Baek5, Geun-Tae Kim6

Department of Internal Medicine, Pusan National University School of Medicine1, Busan, Malgeunsem Hospital2, Changwon, Young-do Hospital3, Busan St. Mary’s Medical Center4, Division of Rheumatology, Department of Internal Medicine, Ilsin Christian Hospital5, Division of Rheumatology, Department of Internal Medicine, Kosin University College of Medicine6, Busan, Korea

Correspondence to:Seung-Hoon Baek

Received: October 17, 2012; Accepted: November 7, 2012

Abstract

Treatments for patient with ankylosing spondylitis (AS) include non-steroidal anti-inflammatory drugs (NSAIDs), disease-modifying antirheumatic drugs (DMARDs) and anti-tumor necrosis factor-alpha (TNFα) agents. However, owing to the well-known nephrotoxicity of NSAIDs and some DMARDs, the use of these drugs is limited in AS patients with renal insufficiency. As the pharmacokinetics and metabolism of anti-TNFα agents in patients of end stage renal disease, especially those receiving peritoneal dialysis (PD), have not been investigated well, little is known about treating them with anti-TNFα agents. We described the safety and efficacy of etanercept, a soluble fusion protein comprising the TNF receptor 2 in linkage with the Fc portion of immunoglobulin G, in a 40-year-old male AS patient receiving PD.

Keywords: Ankylosing spondylitis, End-stage renal disease, Peritoneal dialysis, Tumor necrosis factor-alpha

JRD
Oct 01, 2024 Vol.31 No.4, pp. 191~263
COVER PICTURE
Ancestry-driven pathways for SLE-risk SNP-associated genes. The ancestry-driven key signaling pathways in Asians, Europeans, and African Americans were analyzed by enrichr (https://maayanlab.cloud/Enrichr/#libraries) using non-HLA SNP-associated genes. SLE: systemic lupus erythematosus, SNP: single-nucleotide polymorphism, JAK–STAT: janus kinase–signal transducers and activators of transcription, IFN: interferon gamma. (J Rheum Dis 2024;31:200-211)

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