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补骨脂素加紫外线A疗法中最小光毒性剂量预测的改进

Improved prediction of the minimal phototoxic dose in PUVA therapy.

作者信息

Sakuntabhai A, Matthews J N, Farr P M

机构信息

Department of Dermatology, Royal Victoria Infirmary, Newcastle upon Tyne, U.K.

出版信息

Br J Dermatol. 1994 May;130(5):604-9. doi: 10.1111/j.1365-2133.1994.tb13107.x.

Abstract

In an attempt to improve the prediction of PUVA erythemal sensitivity, we have examined, in 251 patients, the relationship between the minimal phototoxic dose (MPD) and a number of variables, including skin type, ingested dose of 8-methoxypsoralen (8-MOP) and history of previous PUVA treatment. The MPD was determined by phototesting 2 h after ingestion of crystalline 8-MOP, given at a standard dose of 0.6 mg/kg (calculated to the nearest 10 mg). No reaction to the highest dose of UVA used for phototesting occurred in 16% of cases; the dose of 8-MOP was significantly associated with non-response. In the patients in whom an erythemal response was obtained, a significant association was found between the MPD and the variables of skin type, ingested dose of 8-MOP, and history of previous PUVA treatment. Thus, by taking these factors into account, a more accurate prediction can be made of an individual patient's erythemal sensitivity to PUVA than relying on skin type alone. That erythemal sensitivity is affected by the ingested dose of 8-MOP (even when all patients received 0.6 mg/kg) suggests that conventional psoralen dosing according to body weight is not ideal.

摘要

为了提高对补骨脂素紫外线A(PUVA)红斑敏感性的预测,我们对251例患者进行了研究,检测了最小光毒性剂量(MPD)与多个变量之间的关系,这些变量包括皮肤类型、8-甲氧基补骨脂素(8-MOP)的摄入剂量以及既往PUVA治疗史。MPD是在摄入结晶状8-MOP 2小时后通过光试验确定的,8-MOP的标准剂量为0.6mg/kg(四舍五入至最接近的10mg)。16%的病例对用于光试验的最高剂量紫外线A无反应;8-MOP的剂量与无反应显著相关。在获得红斑反应的患者中,发现MPD与皮肤类型、8-MOP摄入剂量和既往PUVA治疗史等变量之间存在显著关联。因此,考虑到这些因素,相比于仅依靠皮肤类型,能够更准确地预测个体患者对PUVA的红斑敏感性。红斑敏感性受8-MOP摄入剂量的影响(即使所有患者均接受0.6mg/kg),这表明根据体重进行传统的补骨脂素给药并不理想。

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