Division of Rheumatology, Gulhane Military School of Medicine, Ankara, Turkey.
J Nephrol. 2010 Jan-Feb;23(1):119-23.
Reactive systemic (AA) amyloidosis leading to renal failure is the most severe complication of tumor necrosis factor receptor-associated periodic syndrome (TRAPS). There is now growing evidence to suggest that anti-tumor necrosis factor (anti-TNF) agents may be an attractive treatment option for amyloidosis not only in TRAPS but in several forms of secondary amyloidosis complicating inflammatory rheumatic diseases. In most of the reported cases, anti-TNF agents were deemed successful on the basis of regression of proteinuria and either improvement or stabilization of creatinine clearance, while objective proof of renal amyloid regression either by serum amyloid P scintigraphy or biopsy is limited. We herein report a case of TRAPS complicated with nephrotic syndrome due to AA amyloidosis in which treatment with etanercept was associated with remission of the nephrotic syndrome but no regression of amyloid mass on the follow-up renal biopsy. Indeed, amyloid deposition was noted to be more pronounced on the second renal biopsy, particularly at tubular basement membranes. Although the variable relation between reduction in amyloid load and changes in organ function is well-known, the basis for renal recovery in association with stable or even progressive amyloid deposition is challenging. We suggest that in patients with secondary AA amyloidosis, mechanisms other than the reduction of amyloid mass could have contributed to the observed improvement of renal function with anti-TNF agents.
反应性系统性(AA)淀粉样变性导致肾衰竭是肿瘤坏死因子受体相关周期性综合征(TRAPS)最严重的并发症。现在有越来越多的证据表明,抗肿瘤坏死因子(抗 TNF)药物可能是一种有吸引力的治疗选择,不仅在 TRAPS 中,而且在几种并发炎症性风湿病的继发性淀粉样变性中也是如此。在大多数报道的病例中,抗 TNF 药物被认为是成功的,基于蛋白尿的消退和肌酐清除率的改善或稳定,而通过血清淀粉样蛋白 P 闪烁扫描或活检证实肾脏淀粉样变性的消退是有限的。我们在此报告一例 TRAPS 并发 AA 淀粉样变性肾病综合征,依那西普治疗后肾病综合征缓解,但肾脏活检随访时淀粉样物质无消退。事实上,第二次肾活检时发现淀粉样物质沉积更加明显,特别是在肾小管基底膜。尽管众所周知,淀粉样物质负荷减少与器官功能变化之间的关系是可变的,但与稳定甚至进行性淀粉样物质沉积相关的肾脏恢复的基础是具有挑战性的。我们认为,在继发性 AA 淀粉样变性患者中,除了淀粉样物质减少外,其他机制可能有助于观察到抗 TNF 药物治疗后肾功能的改善。