Erzurum S C, Leff J A, Cochran J E, Ackerson L M, Szefler S J, Martin R J, Cott G R
National Jewish Center for Immunology and Respiratory Medicine, Denver, Colorado.
Ann Intern Med. 1991 Mar 1;114(5):353-60. doi: 10.7326/0003-4819-114-5-353.
To determine the effect of low-dose methotrexate in asthmatic patients on steroid use, asthma symptom scores, pulmonary function, airway reactivity, blood cellular components, and immunoglobulin E levels.
A randomized, double-blind, parallel, placebo-controlled, 13-week clinical trial with follow-up of patients in an open trial of methotrexate at the conclusion of the double-blind study.
An asthma care outpatient clinic.
From February 1988 to March 1990, 19 patients with severe, steroid-dependent asthma were enrolled in the study. Two of these patients were excluded from analysis.
Patients were administered methotrexate or placebo intramuscularly, to assure complete absorption, once weekly during the 13-week study.
Patients on methotrexate and placebo both significantly decreased their steroid dose by 39.6% (95% CI, 25.1% to 54.1%, P = 0.001) and 40.2% (CI, 17.9% to 67.4%, P = 0.003), respectively. Pulmonary function did not differ significantly between the methotrexate and placebo groups. In addition, airway reactivity and symptom scores were unchanged on methotrexate or placebo. No significant toxicities were seen during the course of the 13-week blinded study, but one patient on methotrexate and prednisone in the follow-up period developed Pneumocystis carinii pneumonia and died. Despite continuing methotrexate for up to 1 year, and increasing methotrexate to 30 mg weekly, no significant benefit of methotrexate on asthma control could be shown.
Our study does not support the use of methotrexate in the treatment of severe asthma.
确定低剂量甲氨蝶呤对哮喘患者使用类固醇药物、哮喘症状评分、肺功能、气道反应性、血细胞成分及免疫球蛋白E水平的影响。
一项随机、双盲、平行、安慰剂对照的13周临床试验,在双盲研究结束后对患者进行甲氨蝶呤开放试验随访。
一家哮喘护理门诊。
1988年2月至1990年3月,19例重度、依赖类固醇的哮喘患者纳入研究。其中2例患者被排除在分析之外。
在为期13周的研究中,患者每周接受一次甲氨蝶呤或安慰剂肌肉注射,以确保完全吸收。
接受甲氨蝶呤和安慰剂治疗的患者,其类固醇剂量分别显著降低了39.6%(95%CI,25.1%至54.1%,P = 0.001)和40.2%(CI,17.9%至67.4%,P = 0.003)。甲氨蝶呤组和安慰剂组的肺功能无显著差异。此外,使用甲氨蝶呤或安慰剂时气道反应性和症状评分未改变。在为期13周的盲法研究过程中未观察到显著毒性,但1例在随访期接受甲氨蝶呤和泼尼松治疗的患者发生卡氏肺孢子虫肺炎并死亡。尽管持续使用甲氨蝶呤长达1年,并将甲氨蝶呤剂量增至每周30毫克,但未显示出甲氨蝶呤对哮喘控制有显著益处。
我们的研究不支持使用甲氨蝶呤治疗重度哮喘。