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Methotrexate treatment in patients with adult onset Stills disease—retrospective study of 13 Japanese cases

机译:甲氨蝶呤治疗成年Still病患者的回顾性研究-13例日本病例

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摘要

OBJECTIVE—To evaluate methotrexate treatment in patients with active adult onset Still's disease (AOSD).
METHODS—Methotrexate was initially given as a single weekly oral dose of 5 mg and adjusted individually afterwards in 13 patients with active AOSD. Symptoms and laboratory findings were investigated.
RESULTS—Signs of AOSD activity disappeared (remission) in eight patients between 3 and 16 weeks after starting methotrexate. In these patients, significant improvements in C reactive protein, erythrocyte sedimentation rate, white blood count, and serum ferritin were observed at 8, 12, 14, and 16 weeks after starting methotrexate, respectively. In six of these eight patients, steroids or non-steroidal anti-inflammatory drugs could be reduced or discontinued. In four patients methotrexate was not effective despite 12 or 16 weeks of treatment, and one patient discontinued treatment after 2 weeks because of severe nausea. Five patients suffered from adverse reactions, including acute interstitial pneumonia (one patient) and liver toxicity (two patients). Five out of eight patients successfully treated with methotrexate were HLA-DR4 positive (four homozygotes), and all the unsuccessfully treated patients were DR2 positive.
CONCLUSIONS—Methotrexate is useful for controlling disease activity in AOSD, not only for refractory patients but also for patients who have never taken steroids or for those with steroid associated toxicity. However, serious adverse reactions can occur, as with rheumatoid arthritis. It is important to determine the critical factors, such as the immunogenetic background, that are associated with response to methotrexate treatment.

机译:目的-为评估活动性成人发作性Still病(AOSD)患者的甲氨蝶呤治疗。
方法-甲氨蝶呤最初为每周一次5 mg口服剂量,此后在13例活动性AOSD患者中分别进行调整。调查症状和实验室检查结果。
结果-甲氨蝶呤开始后3周至16周内,有8例患者的AOSD活性消失(缓解)。在这些患者中,甲氨蝶呤开始后第8、12、14和16周分别观察到C反应蛋白,红细胞沉降率,白血球计数和血清铁蛋白显着改善。在这八名患者中的六名中,类固醇或非类固醇抗炎药可以减少或停用。尽管有12或16周的治疗,但4例甲氨蝶呤仍然无效; 2周后有1例患者由于严重的恶心而中止治疗。五例患者出现不良反应,包括急性间质性肺炎(一名患者)和肝毒性(两名患者)。在成功接受甲氨蝶呤治疗的八名患者中,有五名HLA-DR4阳性(四个纯合子),所有未成功治疗的患者均为DR2阳性。
结论:甲氨蝶呤不仅可用于控制难治性患者,而且可用于控制AOSD的疾病活动也适用于从未服用过类固醇的患者或患有类固醇相关毒性的患者。但是,与类风湿关节炎一样,可能会发生严重的不良反应。确定与甲氨蝶呤治疗反应相关的关键因素(例如免疫遗传背景)非常重要。

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