T. Fujii et al., METHOTREXATE TREATMENT IN PATIENTS WITH ADULT-ONSET STILLS-DISEASE - RETROSPECTIVE STUDY OF 13 JAPANESE CASES, Annals of the Rheumatic Diseases, 56(2), 1997, pp. 144-148
Objective-To evaluate methotrexate treatment in patients with active a
dult onset Still's disease (AOSD). Methods-Methotrexate was initially
given as a single weekly oral dose of 5 mg and adjusted individually a
fterwards in 13 patients with active AOSD. Symptoms and laboratory fin
dings were investigated. Results-Signs of AOSD activity disappeared (r
emission) in eight patients between 3 and 16 weeks after starting meth
otrexate. In these patients, significant improvements in C reactive pr
otein, erythrocyte sedimentation rate, white blood count, and serum fe
rritin were observed at 8, 12, 14, and 16 weeks after starting methotr
exate, respectively. In six of these eight patients, steroids or non-s
teroidal 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 becau
se of severe nausea. Five patients suffered from adverse reactions, in
cluding acute interstitial pneumonia (one patient) and liver toxicity
(two patients). Five out of eight patients successfully treated with m
ethotrexate were HLA-DR4 positive (four homozygotes), and all the unsu
ccessfully treated patients were DR2 positive. Conclusions-Methotrexat
e is useful for controlling disease activity in AOSD, not only for ref
ractory patients but also for patients who have never taken steroids o
r 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.