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类风湿关节炎甲氨蝶呤治疗期间补充叶酸。一项双盲、安慰剂对照试验。

Supplementation with folic acid during methotrexate therapy for rheumatoid arthritis. A double-blind, placebo-controlled trial.

作者信息

Morgan S L, Baggott J E, Vaughn W H, Austin J S, Veitch T A, Lee J Y, Koopman W J, Krumdieck C L, Alarcón G S

机构信息

Birmingham Veteran's Administration Hospital, Alabama.

出版信息

Ann Intern Med. 1994 Dec 1;121(11):833-41. doi: 10.7326/0003-4819-121-11-199412010-00002.

Abstract

OBJECTIVE

To determine the effect of two different weekly doses of folic acid on the toxicity and efficacy of low-dose methotrexate therapy for rheumatoid arthritis.

DESIGN

Randomized, double-blind, placebo-controlled study.

PATIENTS

79 persons between 19 and 78 years of age who fulfilled the American Rheumatism Association's criteria for rheumatoid arthritis.

INTERVENTION

Participants were randomly assigned to visually identical placebo or to 5 mg or 27.5 mg of folic acid each week.

MEASUREMENTS

Duration, intensity, and clinical severity of toxic events; efficacy (indices of joint tenderness and swelling and grip strength); plasma and erythrocyte folate levels; and other laboratory variables.

RESULTS

Folic acid supplementation at either dose did not affect the efficacy of methotrexate therapy as judged by joint indices and patient and physician assessments of disease. Patients given folic acid supplements had lower toxicity scores than did participants given placebo (P < or = 0.001). Low blood folate levels and increased mean corpuscular volumes were associated with substantial methotrexate toxicity, whereas daily dietary intakes of more than 900 nmol (400 micrograms) of folic acid were associated with little methotrexate toxicity.

CONCLUSIONS

Folic acid, an inexpensive vitamin, is safe in a broad range of doses and protects patients with rheumatoid arthritis who are taking methotrexate from toxicity while preserving the efficacy of methotrexate.

摘要

目的

确定两种不同每周剂量的叶酸对类风湿关节炎低剂量甲氨蝶呤治疗的毒性及疗效的影响。

设计

随机、双盲、安慰剂对照研究。

患者

79名年龄在19至78岁之间且符合美国风湿病协会类风湿关节炎标准的患者。

干预

参与者被随机分配至外观相同的安慰剂组,或每周服用5毫克或27.5毫克叶酸组。

测量指标

毒性事件的持续时间、强度及临床严重程度;疗效(关节压痛、肿胀及握力指数);血浆及红细胞叶酸水平;以及其他实验室变量。

结果

根据关节指数以及患者和医生对疾病的评估判断,两种剂量的叶酸补充均未影响甲氨蝶呤治疗的疗效。服用叶酸补充剂的患者毒性评分低于服用安慰剂的参与者(P≤0.001)。低血叶酸水平及平均红细胞体积增加与显著的甲氨蝶呤毒性相关,而每日膳食叶酸摄入量超过900纳摩尔(400微克)与甲氨蝶呤毒性较小相关。

结论

叶酸作为一种廉价的维生素,在广泛的剂量范围内是安全的,可保护服用甲氨蝶呤的类风湿关节炎患者免受毒性影响,同时保持甲氨蝶呤的疗效。

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