Department of Internal Medicine, APHP, Tenon Hospital, Sorbonne University, GRC GRAASU, Paris, France.
National Reference Center for Autoinflammatory Diseases and Inflammatory Amyloidosis (CeRéMAIA).
Rheumatology (Oxford). 2021 Dec 1;60(12):5775-5784. doi: 10.1093/rheumatology/keab252.
TNF receptor-1-associated periodic syndrome (TRAPS) is a rare autosomal dominant autoinflammatory disorder associated with mutations in the TNF receptor super family 1 A (TNFRSF1A) gene. AA amyloidosis (AA) is the most severe complication of TRAPS. To study the occurrence and prognosis of AA in TRAPS, we conducted a retrospective study of all French cases and a systematic literature review.
This case series includes TRAPS patients followed by our centre from 2000 to 2020 presenting with histologically confirmed AA. We conducted a systematic literature review on the PubMed and EMBASE databases for articles published up to February 2021 following the Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines and using the keywords: amyloidoisis, amyloid, TNF receptor-associated periodic syndrome, TNF receptor-associated periodic syndrome, tumor necrosis factor receptor-associated periodic syndrome, TRAPS, TNFRSF1A, familial hibernian fever and hibernian familial fever.
A total of 41 TRAPS with AA were studied: three new patients and 38 cases from the literature. AA diagnosis preceded that of TRAPS in 96% of cases, and 17/36 (47%) required renal replacement therapy. Death occurred in 5/36 (14%) with a median follow-up of 23 months. Effect of biologics on AA were available for 21 regimens in 19 patients: 10 improved renal function, seven stabilized and four worsened. Four patients (36% of transplanted patients) relapse AA on kidney graft (only one under etanercept).
TRAPS is revealed by AA in most cases. Therefore, clinical features of TRAPS should be screened for in AA patients. IL-1 antagonist can help to normalize inflammation and to preserve renal function.
肿瘤坏死因子受体-1 相关周期性综合征(TRAPS)是一种罕见的常染色体显性自身炎症性疾病,与肿瘤坏死因子受体超家族 1A(TNFRSF1A)基因的突变有关。AA 淀粉样变性(AA)是 TRAPS 最严重的并发症。为了研究 TRAPS 中 AA 的发生和预后,我们对所有法国病例进行了回顾性研究,并进行了系统的文献复习。
本病例系列包括 2000 年至 2020 年在我们中心就诊的经组织学证实存在 AA 的 TRAPS 患者。我们按照系统评价和荟萃分析的首选报告项目指南,在 PubMed 和 EMBASE 数据库中进行了系统的文献复习,使用的关键词为:amyloidoisis、amyloid、TNF receptor-associated periodic syndrome、TNF receptor-associated periodic syndrome、tumor necrosis factor receptor-associated periodic syndrome、TRAPS、TNFRSF1A、familial hibernian fever 和 hibernian familial fever。
共研究了 41 例 TRAPS 合并 AA:3 例为新患者,38 例为文献病例。AA 的诊断先于 TRAPS 的诊断,占 96%,17/36(47%)需要肾脏替代治疗。36 例中有 5 例(14%)死亡,中位随访时间为 23 个月。19 例患者的 21 种生物制剂治疗方案的 AA 疗效可评估:10 例改善了肾功能,7 例稳定,4 例恶化。4 例(移植患者的 36%)在肾移植后复发 AA(仅 1 例在依那西普治疗下)。
TRAPS 大多由 AA 引起。因此,AA 患者应筛查 TRAPS 的临床特征。白细胞介素-1 拮抗剂有助于使炎症正常化并维持肾功能。