Capell H A, Madhok R, Hunter J A, Porter D, Morrison E, Larkin J, Thomson E A, Hampson R, Poon F W
Centre for Rheumatic Diseases, Glasgow Royal Infirmary, North Glasgow University NHS Trust, Castle St, Glasgow G40SF, UK.
Ann Rheum Dis. 2004 Jul;63(7):797-803. doi: 10.1136/ard.2003.014050.
Evidence for disease modifying activity of low dose corticosteroid treatment in rheumatoid arthritis is contradictory. Studies showing radiological benefit suggest that continued treatment is required to sustain the effect.
To evaluate the effect of low dose oral prednisolone in early rheumatoid arthritis on disease activity over two years.
Double blind placebo controlled trial.
Patients with rheumatoid arthritis, duration <3 years (n = 167), were started on a disease modifying antirheumatic drug (DMARD; sulphasalazine) and allocated by stratified randomisation to prednisolone 7 mg/day or placebo. Primary outcome measure was radiological damage, assessed by the modified Sharp method. Clinical benefit was a secondary outcome. A proactive approach to identifying and treating corticosteroid adverse events was adopted. Patients who discontinued sulphasalazine were offered an alternative DMARD.
90 of 257 patients eligible for the study refused to participate (more women than men). Of those enrolled, 84% were seropositive for rheumatoid factor, median age 56 years, median disease duration 12 months, female to male ratio 1.8:1. Prednisolone was given to 84 patients; of these 73% continued prednisolone and 70% sulphasalazine at 2 years. Of the 83 patients on placebo, 80% continued placebo and 64% sulphasalazine at 2 years. There were no significant differences in radiological score or clinical and laboratory measures at 0 and 2 years.
Low dose prednisolone conferred no radiological or clinical benefit on patients maintained on a DMARD over two years. Low dose corticosteroids have no role in the routine management of rheumatoid arthritis treated with conventional disease modifying drugs.
低剂量糖皮质激素治疗类风湿关节炎的疾病改善活性证据相互矛盾。显示有放射学益处的研究表明,需要持续治疗以维持疗效。
评估低剂量口服泼尼松龙在两年内对早期类风湿关节炎疾病活动的影响。
双盲安慰剂对照试验。
类风湿关节炎病程<3年的患者(n = 167)开始使用改善病情抗风湿药(DMARD;柳氮磺胺吡啶),并通过分层随机分组,分为7毫克/天泼尼松龙组或安慰剂组。主要结局指标为放射学损伤,采用改良Sharp方法评估。临床益处为次要结局指标。采用积极主动的方法识别和治疗糖皮质激素不良事件。停用柳氮磺胺吡啶的患者换用另一种DMARD。
257名符合研究条件的患者中有90名拒绝参与(女性多于男性)。入组患者中,84%类风湿因子血清学阳性,中位年龄56岁,中位病程12个月,男女比例为1.8:1。84名患者接受泼尼松龙治疗;其中73%在2年时继续使用泼尼松龙,70%继续使用柳氮磺胺吡啶。83名服用安慰剂的患者中,80%在2年时继续服用安慰剂,64%继续使用柳氮磺胺吡啶。0年和2年时,放射学评分、临床及实验室指标均无显著差异。
对于接受DMARD治疗两年的患者,低剂量泼尼松龙未带来放射学或临床益处。低剂量糖皮质激素在常规使用改善病情药物治疗的类风湿关节炎的常规管理中无作用。