Methotrexate treatment in patients with adult onset Still's disease - Retrospective study of 13 Japanese cases

被引:58
作者
Fujii, T [1 ]
Akizuki, M [1 ]
Kameda, H [1 ]
Matsumura, M [1 ]
Hirakata, M [1 ]
Yoshida, T [1 ]
Shinozawa, T [1 ]
Mimori, T [1 ]
机构
[1] KEIO UNIV,SCH MED,DIV RHEUMATOL,DEPT INTERNAL MED,TOKYO 160,JAPAN
关键词
D O I
10.1136/ard.56.2.144
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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.
引用
收藏
页码:144 / 148
页数:5
相关论文
共 14 条
[1]  
AYDINTUG AO, 1992, J RHEUMATOL, V19, P431
[2]   STILL,S DISEASE IN ADULT [J].
BYWATERS, EG .
ANNALS OF THE RHEUMATIC DISEASES, 1971, 30 (02) :121-+
[3]  
CHANG DM, 1992, J RHEUMATOL, V19, P1678
[4]  
CONTOR JP, 1987, CHEST, V92, P939
[5]   ADULT-ONSET STILLS DISEASE WITH AN ASSOCIATED SEVERE RESTRICTIVE PULMONARY DEFECT - A CASE-REPORT [J].
CORBETT, AJ ;
ZIZIC, TM ;
STEVENS, MB .
ANNALS OF THE RHEUMATIC DISEASES, 1983, 42 (04) :452-454
[6]  
KRAUS A, 1991, J RHEUMATOL, V18, P918
[7]  
OHTA A, 1987, J RHEUMATOL, V14, P1139
[8]   ADULT STILLS DISEASE - MANIFESTATIONS, DISEASE COURSE, AND OUTCOME IN 62 PATIENTS [J].
POUCHOT, J ;
SAMPALIS, JS ;
BEAUDET, F ;
CARETTE, S ;
DECARY, F ;
SALUSINSKYSTERNBACH, M ;
HILL, RO ;
GUTKOWSKI, A ;
HARTH, M ;
MYHAL, D ;
SENECAL, JL ;
YEADON, C ;
ESDAILE, JM .
MEDICINE, 1991, 70 (02) :118-136
[9]  
ROGERS JT, 1990, J BIOL CHEM, V265, P14572
[10]   EVALUATION OF SERUM FERRITIN AS A MARKER FOR ADULT STILL DISEASE-ACTIVITY [J].
SCHWARZEYWILL, M ;
HEILIG, B ;
BAUER, H ;
BREITBART, A ;
PEZZUTTO, A .
ANNALS OF THE RHEUMATIC DISEASES, 1992, 51 (05) :683-685