Liebling M R, Leib E, McLaughlin K, Blocka K, Furst D E, Nyman K, Paulus H E
Ann Intern Med. 1981 Jan;94(1):21-6. doi: 10.7326/0003-4819-94-1-21.
Ten patients with rheumatoid arthritis unresponsive to conventional therapy participated in a double-blind cross-over trial in which they randomly received either a "pulse" or 1 g of methylprednisolone or placebo, intravenously, once a month for 6 months. Both the drug-first and placebo-first groups had the same mean American Rheumatism Association functional classification, 2.5. During the study patients on methylprednisolone "pulses," compared to placebo, showed significantly better mean tender-joint counts, walking times, and grip strength (p < 0.05). The drug-treated patients also had significantly lower levels of immune complexes (p < 0.01) and IgG (p < 0.01). Effects could still be measured an average of 2.9 +/- 0.4 months after the last dose of methylprednisolone. No significant side effects were noted during the therapy. Despite these findings, "pulse" methylprednisolone did not appear to significantly retard radiologic progression of the arthritis.
10名对传统疗法无反应的类风湿性关节炎患者参与了一项双盲交叉试验,试验中他们被随机给予“冲击”疗法、1克甲基强的松龙或安慰剂,每月静脉注射一次,共6个月。先接受药物治疗组和先接受安慰剂治疗组的美国风湿病协会功能分级均值相同,均为2.5级。在研究过程中,与安慰剂组相比,接受甲基强的松龙“冲击”疗法的患者在平均压痛关节数、步行时间和握力方面表现出显著更好的效果(p < 0.05)。接受药物治疗的患者免疫复合物水平(p < 0.01)和IgG水平(p < 0.01)也显著更低。在最后一剂甲基强的松龙注射后平均2.9 +/- 0.4个月仍可检测到效果。治疗期间未发现明显副作用。尽管有这些发现,但“冲击”疗法的甲基强的松龙似乎并未显著减缓关节炎的放射学进展。