Balduzzi Silvia, Scirè Carlo Alberto, Sakellariou Garifallia, Benaglio Francesca, Bugatti Serena, Montecucco Carlomaurizio, Caporali Roberto
Division of Rheumatology, IRCCS Policlinico San Matteo Foundation, University of Pavia, Italy.
Italian Society for Rheumatology (SIR), Epidemiology Unit, Milan, Italy.
Clin Exp Rheumatol. 2017 May-Jun;35(3):401-405. Epub 2016 Dec 13.
The aim of this study was to compare the 12-month probability of remission in early inflammatory arthritis with a milder treatment based on the 1987 criteria or a more intensive protocol based on the 2010 criteria.
Patients with rheumatoid arthritis (RA) or undifferentiated arthritis (UA) (2005-2012) were included. Before October 2010, patients fulfilling the 1987 criteria received methotrexate (MTX) and possibly low-dose prednisone, while UA hydroxychloroquine (HCQ) (1987-driven cohort). From October 2010, patients fulfilling the 2010 criteria received higher dose MTX and low-dose prednisone, while UA HCQ (2010-driven cohort). Treatment was increased to achieve DAS28 low disease activity. Clinical remission, defined by DAS28, was evaluated at subsequent visits in the whole population. Hazard ratios (HR) adjusted for age, sex, baseline DAS28, symptoms duration, MTX dose and prednisone were calculated by Cox regression.
677 patients were included (468 in 1987-driven cohort, 209 in 2010-driven cohort), with no significant differences in age, gender, autoantibodies and pain. The 2010-driven cohort had significantly fewer tender and swollen joints, lower acute phase reactants, DAS28 and HAQ and achieved more frequently remission even when the analysis was adjusted for all confounders (adjusted HR (95% CI) 1.73 (1.34, 2.22)) and limited to per protocol patients (adjusted HR (95%CI) 1.49 (1.11, 2.02).
Treating patients with early arthritis according to a more intensive protocol leads to higher remission rate. The results of this study support the use of a strategy led by the 2010 criteria with more intensive treatment strategies in the management of early arthritis.
本研究旨在比较基于1987年标准的轻度治疗方案与基于2010年标准的更强化治疗方案在早期炎症性关节炎中实现缓解的12个月概率。
纳入类风湿关节炎(RA)或未分化关节炎(UA)患者(2005 - 2012年)。2010年10月之前,符合1987年标准的患者接受甲氨蝶呤(MTX)治疗,可能联合低剂量泼尼松,而未分化关节炎患者接受羟氯喹(HCQ)治疗(1987年驱动队列)。从2010年10月起,符合2010年标准的患者接受更高剂量的MTX和低剂量泼尼松,而未分化关节炎患者接受HCQ治疗(2010年驱动队列)。增加治疗以达到DAS28低疾病活动度。在整个人群的后续随访中评估由DAS28定义的临床缓解情况。通过Cox回归计算调整年龄、性别、基线DAS28、症状持续时间、MTX剂量和泼尼松后的风险比(HR)。
共纳入677例患者(1987年驱动队列468例,2010年驱动队列209例),在年龄、性别、自身抗体和疼痛方面无显著差异。2010年驱动队列的压痛和肿胀关节明显更少,急性期反应物、DAS28和HAQ更低,即使在对所有混杂因素进行调整后(调整后HR(95%CI)1.73(1.34,2.22)),并且仅限于符合方案的患者(调整后HR(95%CI)1.49(1.11,2.02)),该队列也更频繁地实现缓解。
根据更强化的方案治疗早期关节炎患者可导致更高的缓解率。本研究结果支持在早期关节炎管理中采用以2010年标准为导向的策略及更强化的治疗策略。