Randomized double-blinded placebo-controlled intraindividual trial on topical treatment with a 1,25-dihydroxyvitamin D3 analogue in polymorphic light eruption

被引:41
|
作者
Gruber-Wackernagel, A. [1 ]
Bambach, I. [1 ]
Legat, F. J. [1 ]
Hofer, A. [1 ]
Byrne, S. N. [2 ]
Quehenberger, F. [3 ]
Wolf, P. [1 ]
机构
[1] Med Univ Graz, Res Unit Photodermatol, Dept Dermatol, A-8036 Graz, Austria
[2] Univ Sydney, Dept Immunol & Infect Dis, Sydney Med Sch, Sydney, NSW 2006, Australia
[3] Med Univ Graz, Inst Med Informat Stat & Documentat, A-8036 Graz, Austria
关键词
PSORALEN-PLUS-ULTRAVIOLET; SQUAMOUS-CELL CARCINOMAS; B-EXPOSED SKIN; DENDRITIC CELLS; UV EXPOSURE; IN-VIVO; PSORIASIS; CALCIPOTRIOL; EXPRESSION; SEVERITY;
D O I
10.1111/j.1365-2133.2011.10333.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Polymorphic light eruption (PLE) is a very frequent photodermatosis whose pathogenesis may involve resistance to ultraviolet (UV)-induced immune suppression. Similar to UV radiation, calcitriol (1,25-dihydroxyvitamin D-3) and its analogues such as calcipotriol have been shown to exhibit immunosuppressive properties. Objectives We performed a randomized double-blinded placebo-controlled intraindividual half-body trial (NCT00871052) to investigate the preventive effect of a calcipotriol-containing cream in PLE. Methods Thirteen patients with PLE (10 women, three men; mean age 37 years) pretreated their skin on two symmetrically located test fields with calcipotriol or placebo cream twice daily for 7 days before the start of photoprovocation testing with solar-simulated UV radiation. We established a specific PLE test score [AA + SI + 0.4 P (range 0-12), where AA is affected area score (range 0-4), SI is skin infiltration score (range 0-4) and P is pruritus score on a visual analogue scale (range 0-10)] to quantify PLE severity. Results Photoprovocation led to PLE lesions in 12/13 (92%) patients. As shown by the PLE test score, compared with placebo calcipotrial pretreatment significantly reduced PLE symptoms in average by 32% (95% confidence interval 21-44%; P = 0.0022, exact Wilcoxon signed-rank test) throughout the observation period starting at 48 h until 144 h after the first photoprovocation exposure. At 48, 72 and 144 h calcipotriol pretreatment resulted in a lower PLE test score in 7 (58%), 9 (75%) and 10 (83%) of the 12 cases, respectively. Considering all time points together, calcipotriol diminished the PLE test score in all 12 photoprovocable patients (P = 0.0005; Wilcoxon signed-rank test). Conclusions These results suggest a potential therapeutic benefit of topical 1,25-dihydroxyvitamin D-3 analogues as prophylactic treatment in patients with PLE.
引用
收藏
页码:152 / 163
页数:12
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