Department of Rheumatology and Immunology, Shenzhen Children's Hospital, 7019 Yitian Road, Shenzhen, 518038, China.
Sci Rep. 2023 Jun 3;13(1):9050. doi: 10.1038/s41598-023-36246-6.
Systemic juvenile idiopathic arthritis (SJIA) is a chronic inflammatory disease of childhood with elevated serum IL-6 levels. As an inhibitor of IL-6R, tocilizumab (TCZ) has been approved to treat SJIA patients. TCZ-induced hypofibrinogenemia has been only reported in adult cases and limited small case series with rheumatoid arthritis or giant cell arteritis. Here, we describe the incidence of TCZ-induced hypofibrinogenemia in SJIA patients and its possible influence on bleeding risk. SJIA patients with TCZ treatment in Shenzhen Children's hospital were retrospectively reviewed. Only those with the data on serum fibrinogen levels were included. Data on clinical manifestations, laboratory parameters, management, and sJADAS10-ESR score were collected. Laboratory data were extracted following the start of TCZ therapy at 2, 4, 8, 12, and 24 weeks thereafter. Seventeen SJIA patients with TCZ treatment were included. Thirteen (76.47%, 13/17) had hypofibrinogenemia. The lowest serum fibrinogen levels were even below 1.5 g/L in seven (41.17%, 7/17) patients. Among four patients without MTX treatment, two had obvious hypofibrinogenemia. Although five patients had already stopped steroid treatment 24 weeks after TCZ treatment, three of them still had hypofibrinogenemia. Only P14 had mild nasal mucosal bleeding occasionally. Coagulation tests were regularly performed in eight patients, of these, six had hypofibrinogenemia, which occurred following one to four doses of TCZ; continuation of TCZ treatment hadn't further aggravated hypofibrinogenemia. Serum fibrinogen levels were not decreased consistently with the improvement of sJADAS10-ESR score in more than half of these eight patients. Factor XIII was detected in six patients and none was identified with Factor XIII deficiency. TCZ alone may induce hypofibrinogenemia in SJIA patients. Continuation of TCZ treatment may be safe for most SJIA patients. But for SJIA patients with indications of surgery or complicated with MAS, the risk of hemorrhage should be regularly evaluated during TCZ treatment. The association between TCZ-induced hypofibrinogenemia and factor XIII deficiency remains uncertain.Trial registration: Not applicable; this was a retrospective study.
全身型幼年特发性关节炎(SJIA)是一种儿童慢性炎症性疾病,其血清 IL-6 水平升高。托珠单抗(TCZ)作为 IL-6R 的抑制剂,已被批准用于治疗 SJIA 患者。TCZ 诱导的低纤维蛋白原血症仅在成人病例和有限的小系列类风湿关节炎或巨细胞动脉炎病例中报告过。在这里,我们描述了 SJIA 患者中 TCZ 诱导的低纤维蛋白原血症的发生率及其对出血风险的可能影响。对在深圳市儿童医院接受 TCZ 治疗的 SJIA 患者进行了回顾性研究。仅纳入了有血清纤维蛋白原水平数据的患者。收集了临床表现、实验室参数、治疗和 sJADAS10-ESR 评分的数据。从 TCZ 治疗开始后 2、4、8、12 和 24 周后提取实验室数据。纳入了 17 例接受 TCZ 治疗的 SJIA 患者。13 例(76.47%,13/17)有低纤维蛋白原血症。7 例(41.17%,7/17)患者的最低血清纤维蛋白原水平甚至低于 1.5g/L。在 4 例未接受 MTX 治疗的患者中,有 2 例有明显的低纤维蛋白原血症。尽管 5 例患者在 TCZ 治疗 24 周后已停止使用类固醇治疗,但其中 3 例仍有低纤维蛋白原血症。只有 P14 偶尔有轻度鼻粘膜出血。8 例患者定期进行凝血试验,其中 6 例有低纤维蛋白原血症,发生在 TCZ 治疗 1 至 4 剂后;继续 TCZ 治疗并未进一步加重低纤维蛋白原血症。在这 8 例患者中,超过一半的患者的血清纤维蛋白原水平并没有随着 sJADAS10-ESR 评分的改善而持续下降。在 6 例患者中检测到了因子 XIII,均未发现因子 XIII 缺乏。TCZ 单独可能会引起 SJIA 患者的低纤维蛋白原血症。对于大多数 SJIA 患者,继续 TCZ 治疗可能是安全的。但是对于有手术指征或伴有 MAS 的 SJIA 患者,在 TCZ 治疗期间应定期评估出血风险。TCZ 诱导的低纤维蛋白原血症与因子 XIII 缺乏之间的关联仍不确定。
不适用;这是一项回顾性研究。