Outcome and treatment of bucillamine-induced nephropathy

被引:7
作者
Hoshino, Junichi
Ubara, Yoshifumi
Hara, Shigeo
Suwabe, Tatsuya
Sawa, Naoki
Tagami, Tetsuo
Katori, Hideyuki
Takemoto, Fumi
Hara, Shigeko
Takaichi, Kenmei
机构
[1] Toranomon Gen Hosp, Nephrol Ctr, Minato Ku, Tokyo 1058470, Japan
[2] Toranomon Gen Hosp, Dept Pathol, Minato Ku, Tokyo 1058470, Japan
来源
NEPHRON CLINICAL PRACTICE | 2006年 / 104卷 / 01期
关键词
bucillamine; nephropathy; membranous; outcome; treatment;
D O I
10.1159/000093254
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Bucillamine (BCL), a treatment for rheumatoid arthritis, occasionally causes proteinuria. Renal specimens are reported to show segmental granular deposition of immunoglobulin G, associated with membranous nephropathy. Long-term course and optimal treatment have remained unknown, and were investigated here. Methods: We examined clinical records of 400 patients treated with BCL for rheumatoid arthritis, at our hospital from 1998 to 2003, finding 17 with proteinuria and biopsy-proven BCL-induced nephropathy. Results: In all 17 patients, proteinuria resolved without loss of renal function between 3 and 85 months after discontinuing BCL (14.1 +/- 3.4). The only factor influencing time to remission was pathologic stage of membranous nephropathy (stage I vs. stage II or III: 11.5 +/- 4.8 vs. 21.6 +/- 3.3 months; p = 0.02). Maximal proteinuria, total amount of BCL, BCL exposure time, and use of prednisolone or other immunosuppressant agents did not significantly influence time until remission. Conclusion: The most important therapeutic step in treating BCL-induced nephropathy is to discontinueBCL. Prednisolone or other immunosuppressant agents might not be effective. Copyright (c) 2006 S. Karger AG, Basel.
引用
收藏
页码:C15 / C19
页数:5
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