Alberdi-Saugstrup Mikel, Nielsen Susan, Mathiessen Pernille, Nielsen Claus Henrik, Müller Klaus
Department of Pediatrics, Naestved Hospital, Naestved, Denmark.
Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Clin Rheumatol. 2017 Jan;36(1):67-75. doi: 10.1007/s10067-016-3375-x. Epub 2016 Aug 25.
Two thirds of patients with juvenile idiopathic arthritis (JIA) treated with tumor necrosis factor (TNF)-alpha inhibitors respond initially, but only about one third of patients achieve clinical remission at follow-up. We evaluated the 1-year response and long-term treatment adherence to TNF inhibitor treatment in JIA patients naive to biologics and investigated if baseline myeloid-related protein (MRP)-8/14 and C-reactive protein (CRP) were predictive of treatment response. One hundred fifty-two patients were included in a unicenter observational, prospective study from 2002 to 2015, excluding patients with systemic-onset JIA. One-year treatment response was evaluated by American College of Rheumatology-pediatric (ACR-ped) and by the number of patients achieving inactive disease (ID). Medical charts were reviewed for reasons of treatment withdrawal. After one year of treatment ACR-ped 30, 50, 70, and 90 were achieved by 61, 55, 38, and 10 % of the patients, and 23 % achieved a status of ID. Treatment adherence: 51 % withdrew from treatment due to lack of clinical effect, while 32 % continued treatment or withdrew due to disease remission. Increased MRP-8/14 concentrations at treatment initiation was associated with ID after 1 year (OR 1.55, CI 1.06-2.25, p = 0.02). Treatment withdrawal due to lack of effect was associated with low baseline levels of both MRP-8/14 (685 vs. 1235 ng/ml, p < 0.001) and CRP (0.75 vs. 2.73 mg/l, p < 0.001), verified by multivariable logistic regression analysis (OR 0.51, CI 0.34-0.77/OR 0.63, CI 0.48-0.83). In conclusion, an association was found between ID after 1 year of treatment and increased baseline levels of MRP-8/14. Furthermore, low baseline MRP-8/14 and CRP concentrations were associated with treatment withdrawal due to lack of clinical effect.
三分之二接受肿瘤坏死因子(TNF)-α抑制剂治疗的幼年特发性关节炎(JIA)患者最初有反应,但随访时只有约三分之一的患者实现临床缓解。我们评估了未使用过生物制剂的JIA患者对TNF抑制剂治疗的1年反应和长期治疗依从性,并研究基线髓系相关蛋白(MRP)-8/14和C反应蛋白(CRP)是否可预测治疗反应。2002年至2015年,一项单中心观察性前瞻性研究纳入了152例患者,排除全身型JIA患者。通过美国风湿病学会儿科(ACR-ped)标准和达到疾病非活动(ID)状态的患者数量评估1年治疗反应。查阅医疗记录以了解治疗中断原因。治疗1年后,61%、55%、38%和10%的患者达到ACR-ped 30、50、70和90标准,23%的患者达到ID状态。治疗依从性:51%的患者因缺乏临床疗效而停止治疗,32%的患者因疾病缓解而继续治疗或停止治疗。治疗开始时MRP-8/14浓度升高与1年后达到ID相关(比值比[OR]1.55,可信区间[CI]1.06-2.25,p = 0.02)。因缺乏疗效而停止治疗与MRP-8/14(685 vs. 1235 ng/ml,p < 0.001)和CRP(0.75 vs. 2.73 mg/l,p < 0.001)的低基线水平相关,多变量逻辑回归分析证实了这一点(OR 0.51,CI 0.34-0.77/OR 0.63,CI 0.48-0.83)。总之,发现治疗1年后达到ID与MRP-8/14基线水平升高之间存在关联。此外,MRP-8/14和CRP的低基线浓度与因缺乏临床疗效而停止治疗相关。