Jf. Molina et H. Mcgrath, LONG-TERM ULTRAVIOLET-A1 IRRADIATION THERAPY IN SYSTEMIC LUPUS-ERYTHEMATOSUS, Journal of rheumatology, 24(6), 1997, pp. 1072-1074
Objective. In a recent series of short term studies ultraviolet-Al (UV
-A1; 340-400 nm) dermal irradiation proved effective in reducing signs
and symptoms of disease activity in patients with systemic lupus eryt
hematosus (SLE). To determine if the effectiveness persisted with long
term therapy, we followed the progress of 6 of these patients for an a
verage of 3.4 (range 2.4-4.5) yrs. The 6 had had significant decreases
in signs and symptoms of disease activity during the first 12 weeks o
f the earlier studies while receiving 3 to 5 low dose UV-A1 irradiatio
ns weekly and were asked to continue into longterm therapy. Methods. L
ongterm therapy consisted of 1 or 2 irradiations of 6-15 J/m(2) (15-30
min, or about 1/8-1/4 minimal erythema dose) per week. We assessed th
eir progress every 3 mo with the systemic lupus activity measures. Res
ults. Despite the smaller number of weekly treatments, the gains achie
ved during the initial 12 weeks of the early studies not only persiste
d but increased slightly. Tanning was moderate to absent, the therapy
was well tolerated, and there was no apparent toxicity. Conclusion. UV
-AI radiation induced remissions in SLE persist with longterm therapy;
1 or 2 weekly exposures suffice; there appears to be no significant t
oxicity.