肿瘤坏死因子受体相关周期性综合征:斯洛伐克一组trap患者的分析

IF 1.1 Q4 RHEUMATOLOGY
Branislav Slenker, Peter Banovcin, Katarina Hrubiskova, Veronika Vargova, Anna Bobcakova, Dusana Gensor, Eva Malicherova Jurkova, Daniela Kapustova, Lenka Kapustova, Adam Markocsy, Otilia Petrovicova, Milos Jesenak
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引用次数: 0

摘要

背景/目的:肿瘤坏死因子受体相关周期性综合征(TRAPS)是由TNFRSF1A基因突变引起的常染色体显性全身性自身炎症性疾病。TRAPS的临床表现是异质性的,这可能使其诊断复杂化。本研究旨在描述斯洛伐克诊断和治疗的trap患者的临床和遗传特征,以及评估他们对canakinumab的治疗反应。材料与方法:回顾性分析斯洛伐克国家数据库中周期性发热综合征患者的临床数据,其中包括斯洛伐克2019年至2022年诊断的7例TRAPS患者。这些数据与来自欧洲、中国和日本的现有队列研究结果进行了比较。结果:7例患者均为女性,临床发病时中位年龄为6岁(范围:8个月至30岁);1例为成人发病。最常见的症状是反复发作的发热(6/7)、皮疹(6/7)、关节痛(6/7)、肌痛(5/7)、腹痛(4/7)、胸痛(4/7)和全身乏力(4/7)。值得注意的是,1例患者表现出中枢神经系统(CNS)受累,表现为癫痫发作和无菌性中枢神经系统炎症。遗传分析鉴定出TNFRSF1A的4个变异,包括文献中很少报道的N145S变异(也称为N116S)。使用canakinumab治疗可显著降低发作频率和炎症标志物。结论:本研究强调了trap的表型多样性,如鉴定出罕见的TNFRSF1A N145S变异和一例累及中枢神经系统的病例所示。据估计,斯洛伐克的TRAPS患病率约为178万,这些患者的临床特征与欧洲队列报告的相似。此外,对canakinumab的良好治疗反应支持其作为trap有效治疗选择的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

TNF Receptor-Associated Periodic Syndrome: An Analysis of a Slovakian Cohort of TRAPS Patients.

TNF Receptor-Associated Periodic Syndrome: An Analysis of a Slovakian Cohort of TRAPS Patients.

Background/Aims: Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) is an autosomal dominant systemic autoinflammatory disease caused by mutations in the TNFRSF1A gene. The clinical presentation of TRAPS is heterogeneous, which can complicate its diagnosis. This study aimed to characterize the clinical and genetic features of patients with TRAPS diagnosed and treated in Slovakia, as well as to evaluate their therapeutic response to canakinumab. Materials and Methods: A retrospective analysis of clinical data from the Slovak national database of patients with periodic fever syndromes was performed, including 7 TRAPS patients diagnosed between 2019 and 2022 in Slovakia. These data were compared with findings from available cohorts from Europe, China, and Japan. Results: All 7 patients were female, with a median age at clinical disease onset of 6 years (range: 8 months to 30 years); 1 patient had adult-onset disease. The most frequent symptoms were recurrent episodes of fever (6/7), skin rash (6/7), arthralgia (6/7), myalgia (5/7), abdominal pain (4/7), chest pain (4/7), and general fatigue (4/7). Notably, 1 patient exhibited central nervous system (CNS) involvement manifesting as seizures and aseptic CNS inflammation. Genetic analysis identified 4 variants in TNFRSF1A, including the N145S variant (also referred to as N116S), a variant only rarely reported in the literature. Treatment with canakinumab resulted in a significant reduction in flare frequency and decreases in inflammatory markers. Conclusion: This study underscores the phenotypic diversity of TRAPS, as shown by the identification of the rare TNFRSF1A N145S variant and a case with CNS involvement. The estimated prevalence of TRAPS in Slovakia is approximately 1 : 780 000, and the clinical features of these patients are comparable to those reported in European cohorts. Furthermore, the favorable therapeutic response to canakinumab supports its potential as an effective treatment option for TRAPS.

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