Aubin F, Makki S, Humbert P, Muret P, Agache P
Department of Functional Dermatology, University Hospital, Besançon, France.
Arch Dermatol Res. 1994;286(1):30-4. doi: 10.1007/BF00375840.
Since 1974, phototherapy with psoralen and ultraviolet A (UVA) has been used successfully for the treatment of psoriasis. However, undesirable side effects, including phototoxicity, nausea, stomach pain and headaches, have led investigators to develop new psoralen compounds. 5-Methoxypsoralen (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 micronized tablet form (5-MOPm) has been developed. In an open randomized study, oral treatments with 5-MOP or 5-MOPm plus UVA radiation were compared 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) and occurred earlier (51.8 vs 229.09 min) with 5-MOPm. In addition, a reduction in PASI of more than 90% was achieved sooner (10.63 vs 17.27 treatments) and with a lower cumulative UVA dose (145.89 vs 232.11 J/cm2), in the group treated with 5-MOPm. No side effects were observed with 5-MOPm. Our data indicate that 5-MOPm has a higher bioavailability, clinical efficacy and tolerability than the commonly used 5-MOP.
自1974年以来,补骨脂素与紫外线A(UVA)光疗已成功用于治疗银屑病。然而,包括光毒性、恶心、胃痛和头痛在内的不良副作用促使研究人员开发新的补骨脂素化合物。因此,5-甲氧基补骨脂素(5-MOP)作为8-甲氧基补骨脂素(8-MOP)的替代品被引入,因为其副作用较小。由于已知5-MOP的吸收动力学和生物活性存在差异,因此开发了一种新的微粉化片剂形式(5-MOPm)。在一项开放随机研究中,对22例银屑病患者进行了5-MOP或5-MOPm联合UVA照射的口服治疗比较。治疗组之间的皮肤类型和初始银屑病面积严重程度指数无显著差异。5-MOPm的血清浓度显著更高(320 vs 85.82 ng/ml)且出现更早(51.8 vs 229.09分钟)。此外,5-MOPm治疗组更快(10.63 vs 17.27次治疗)且以更低的累积UVA剂量(145.89 vs 232.11 J/cm2)实现了银屑病面积和严重程度指数(PASI)降低超过90%。5-MOPm未观察到副作用。我们的数据表明,5-MOPm比常用的5-MOP具有更高的生物利用度、临床疗效和耐受性。