青少年特发性关节炎非系统性变体儿童治疗结果:缓解、加剧和不良现象。回顾性步兵研究

Михаил Михайлович Костик, И. А. Чикова, Е. А. Исупова, М. Н. Лихачёва, Т. С. Лихачёва, М. Ф. Дубко, В. В. Масалова, Л. С. Снегирёва, Е. В. Гайдар, Ольга Владимировна Калашникова, В. Г. Часнык
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引用次数: 0

摘要

背景。依那西普是一种最常用于幼年特发性关节炎(JIA)患者的生物药物。在当地的研究中显示了它的使用结果。目标。我们的目的是评估依那西普在非系统性JIA患儿中的疗效和安全性,以确定缓解的预测因素和恶化发展的危险因素。方法。在一项回顾性队列研究中,分析了依那西普治疗非系统性JIA儿童的结果(缓解、恶化、不良事件)。最小随访期为6个月。结果。77/131(58.8%)患者在6-36个月内出现缓解期,18/129(14.0%)患者出现恶化。缓解的预测因子为JIA发病年龄< 8岁[相对危险度(RR) 2.05;95%可信区间(CI) 1.27 ~ 3.23],开依那西普年龄≤10岁(RR为1.7,95% CI为1.22 ~ 2.38),开依那西普前患病时间< 2.5年(RR为2.4,95% CI为1.4 ~ 4.4),存在HLA-B27抗原(RR为2.15,95% CI为0.98 ~ 4.75;P = 0.06)。多关节性JIA患儿的恶化风险更高(RR 2.7, 95% CI 0.9-8.2;p = 0.08),而甲氨蝶呤治疗降低了恶化的风险(RR 0.32, 95% CI 0.1-1.15;P = 0.05)。依那西普在14/152(9.2%)患者中因原发性(治疗3个月后ACRpedi标准改善<30%)或继发性(先前达到≥30%的改善丧失)失败而停药;152例患者中有8例(5.3%)发生新发葡萄膜炎;注射部位的反应- 6/152(4.0%)例患者。结论。在发病年龄为8岁且病史小于2.5年的年轻JIA患者中,使用依那西普治疗更有可能诱导缓解。多关节性JIA患者的恶化风险较高,而接受甲氨蝶呤联合治疗的患者的恶化风险较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
РЕЗУЛЬТАТЫ ЛЕЧЕНИЯ ЭТАНЕРЦЕПТОМ ДЕТЕЙ С НЕСИСТЕМНЫМИ ВАРИАНТАМИ ЮВЕНИЛЬНОГО ИДИОПАТИЧЕСКОГО АРТРИТА: ДОСТИЖЕНИЕ РЕМИССИИ, РАЗВИТИЕ ОБОСТРЕНИЙ И НЕЖЕЛАТЕЛЬНЫХ ЯВЛЕНИЙ. РЕТРОСПЕКТИВНОЕ КОГОРТНОЕ ИССЛЕДОВАНИЕ
Background. Etanercept is a biological drug most commonly used in patients with juvenile idiopathic arthritis (JIA). The results of its use are showed in local studies. Objective. Our aim was to evaluate the efficacy and safety of the use of etanercept in children with non-systemic JIA, to determine the predictors of remission and the risk factors for the development of exacerbations. Methods. In a retrospective cohort study, the results of etanercept treatment (remission, exacerbations, adverse events) in children with non-systemic JIA were analyzed. The minimum follow-up period was 6 months. Results. The period of remission within 6–36 months occurred in 77/131 (58.8%), exacerbations developed in 18/129 (14.0%) patients. Predictors of achieving remission were the age of JIA onset < 8 years [relative risk (RR) 2.05; 95% confidence interval (CI) 1.27–3.23], the age of prescribing etanercept ≤ 10 years (RR 1.7, 95% CI 1.22–2.38), the time of the disease prior to etanercept prescription < 2.5 years (RR 2.4, 95% CI 1.4–4.4), the presence of HLA-B27 antigen (RR 2.15, 95% CI 0.98–4.75; p = 0.06). The risk of exacerbations was higher in children with polyarticular JIA (RR 2.7, 95% CI 0.9–8.2; p = 0.08), whereas methotrexate therapy reduced the risk of exacerbations (RR 0.32, 95% CI 0.1–1.15; p = 0.05). Etanercept was discontinued due to primary (improvement by the ACRpedi criteria after 3 months of therapy <30%) or secondary (loss of previously achieved ≥ 30% improvement) failure in 14/152 (9.2%) patients; de novo uveitis developed in 8/152 (5.3%) patients; reactions at the injection site — in 6/152 (4.0%) patients. Conclusion. Therapy involving etanercept is more likely to induce remission in younger patients with JIA onset at the age of 8 years and a history of less than 2.5 years. A high risk of exacerbations was noted in patients with polyarticular JIA, and low one — in those receiving methotrexate as a part of combined therapy.
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