Osswald Delphine, Rameau Anne-Cécile, Terzic Joëlle, Sordet Christelle, Bourcier Tristan, Sauer Arnaud
Service d'Ophtalmologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Service de Pédiatrie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Front Pediatr. 2022 Mar 4;10:802977. doi: 10.3389/fped.2022.802977. eCollection 2022.
Pediatric uveitis is the leading cause of acquired child blindness, due to unremitting inflammation and long-term steroid exposition. Biotherapies with anti-tumor necrosis factor alpha (anti-TNFα) are effective in controlling inflammation for severe pediatric uveitis in recent studies. Major concern of anti-TNFα prescription is the balance between the severity of the disease and side effects of the drug. The aim of the present study is to describe a cohort of children with severe uveitis and to highlight the risk factors for a pejorative development that led to the prescription of anti-TNFα drugs.
A retrospective case-control study was carried out on children with uveitis associated with systemic inflammatory disease or idiopathic uveitis, with a minimum follow-up of 5 years. Anti-TNFα-treated patients (case) were studied and compared with patients who were not requiring anti-TNFα (control). Univariate logistic regression analyses were performed to compare both groups and determine the risk factors for anti-TNFα therapy.
Seventy-three cases of pediatric uveitis were included, 13 cases and 60 controls. The risk factors associated with increased odds of anti-TNFα therapy were initial systemic disorder associated with uveitis [OR = 11.22 (1.37-91.85), = 0.0241), family history of autoimmune diseases [OR = 9.43 (2.27-39.15), = 0.0020], uveitis diagnosis before the age of 6 [OR = 4.05 (1.16-14.13), = 0.0284], eye surgery [OR = 26.22 (2.63-261.77), = 0.0054], ocular complications at the first slit lamp exam [OR = 67.11 (3.78-1191.69), = 0.0042], low visual acuity at diagnosis (≥0.3 logMAR) [OR = 11.76 (2.91-47.62), = 0.0005] and especially low binocular acuity at diagnosis (≥0.3 logMAR) [OR = 8.75 (1.93-39.57), = 0.0048], panuveitis [OR = 9.17 (2.23-37.60), = 0.0021], having positive ANA [OR = 3.89 (1.07-14.11), = 0.0391], and positive HLA B27 [OR = 9.43 (2.27-39.16), = 0.0020].
Those risk factors could be used to establish a new follow-up and treatment schedule for severe uncontrolled uveitis. This could help to better predict the best time to start anti-TNF therapy.
由于炎症持续不缓解以及长期使用类固醇药物,儿童葡萄膜炎是后天性儿童失明的主要原因。近期研究表明,使用抗肿瘤坏死因子α(抗TNFα)的生物疗法对控制重度儿童葡萄膜炎的炎症有效。抗TNFα药物处方的主要关注点在于疾病严重程度与药物副作用之间的平衡。本研究的目的是描述一组患有重度葡萄膜炎的儿童,并突出导致抗TNFα药物处方的病情恶化发展的危险因素。
对患有与全身性炎症性疾病相关的葡萄膜炎或特发性葡萄膜炎的儿童进行了一项回顾性病例对照研究,最短随访时间为5年。对接受抗TNFα治疗的患者(病例组)进行研究,并与不需要抗TNFα治疗的患者(对照组)进行比较。进行单因素逻辑回归分析以比较两组并确定抗TNFα治疗的危险因素。
纳入了73例儿童葡萄膜炎病例,其中13例为病例组,60例为对照组。与抗TNFα治疗几率增加相关的危险因素包括与葡萄膜炎相关的初始全身性疾病[比值比(OR)=11.22(1.37 - 91.85),P = 0.0241]、自身免疫性疾病家族史[OR = 9.43(2.27 - 39.15),P = 0.0020]、6岁前诊断为葡萄膜炎[OR = 4.05(1.16 - 14.13),P = 0.0284]、眼部手术[OR = 26.22(2.63 - 261.77),P = 0.0054]、首次裂隙灯检查时的眼部并发症[OR = 67.11(3.78 - 1191.69),P = 0.0042]诊断时低视力(≥0.3 logMAR)[OR = 11.76(2.91 - 47.62),P = 0.0005],尤其是诊断时双眼低视力(≥0.3 logMAR)[OR = 8.75(1.93 - 39.57),P = 0.0048]、全葡萄膜炎[OR = 9.17(2.23 - 37.60),P = 0.0021]、抗核抗体(ANA)阳性[OR = 3.89(1.07 - 14.11),P = 0.0391]以及人类白细胞抗原B27(HLA B27)阳性[OR = 9.43(2.27 - 39.16),P = 0.0020]。
这些危险因素可用于为重度难治性葡萄膜炎建立新的随访和治疗方案。这有助于更好地预测开始抗TNF治疗的最佳时机。