F. Aubin et al., TREATMENT OF PSORIASIS WITH A NEW MICRONIZED 5-METHOXYPSORALEN TABLETAND UVA RADIATION, Archives of dermatological research, 286(1), 1994, pp. 30-34
Since 1974, phototherapy with psoralen and ultraviolet A (UVA) has bee
n used successfully for the treatment of psoriasis. However, undesirab
le side effects, including phototoxicity, nausea, stomach pain and hea
daches, have led investigators to develop new psoralen compounds. 5-Me
thoxypsoralen (5-MOP) has thus been introduced as an alternative to 8-
MOP because of its less pronounced side effects. Since the absorption
kinetics and bioactivity of 5-MOP are known to be variable, a new micr
onized tablet form (5-MOPm) has been developed. In an open randomized
study, oral treatments with 5-MOP or 5-MOPm plus UVA radiation were co
mpared in 22 psoriatic patients. Skin type and initial psoriasis area
severity index did not differ significantly between treatment groups.
Serum concentrations were significantly higher (320 vs 85.82 ng/ml) an
d occurred earlier (51.8 vs 229.09 min) with 5-MOPm. In addition, a re
duction in PASI of more than 90% was achieved sooner (10.63 vs 17.27 t
reatments) and with a lower cumulative UVA dose (145.89 vs 232.11 J/cm
2), in the group treated with 5-MOPm. No side effects were observed wi
th 5-MOPm. Our data indicate that 5-MOPm has a higher bioavailibility,
clinical efficacy and tolerability than the commonly used 5-MOP.