Calcipotriol ointment versus cream in psoriasis vulgaris.

G Duweb, S Aldebani, A Elzorghany, M Benghazil, J Alhaddar
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Abstract

Psoriasis is a multifactorial, chronically relapsing, inflammatory skin disease occurring in 1-3% of the world's population. Vitamin D3 analogs have effects on proliferation and differentiation, as well as on the infiltration and activation of neutrophils and immunocytes in psoriatic skin lesions. This study aims to assess the efficacy and safety of topical calcipotriol and to compare ointment and cream formulations in the treatment of psoriasis vulgaris. A total of 41 patients with mild to moderate psoriasis vulgaris (18 men and 23 women aged between 5 and 63 years) were enrolled in the study. Each patient was instructed to apply the treatment twice daily over the psoriatic lesions. Routine blood tests and serum calcium were performed prior to and at the end of treatment. Treatment assessment was carried out on weeks 2, 4 and 6 and was based on the Psoriasis Area and Severity Index (PASI) score. Of the 41 patients included in our study, only 29 completed the treatment course. Their PASI before treatment ranged from 1.2 to 43 (mean: 12.1). Both groups, calcipotriol 50 microg/g ointment (11 patients) and calcipotriol 50 microg/g cream (18 patients) showed time-dependent improvement and after 6 weeks there was excellent improvement with a marked reduction in the total mean PASI from 12.1 to 1.02. There was a significant reduction of PASI in the ointment group in comparison with the cream group (mean PASI from 12.7 to 0.8 and 11.1 to 1.15, respectively). No significant adverse effects were observed in either group, except for mild irritation in a few patients in the calcipotriol cream group. In conclusion, calcipotriol was effective, safe and well tolerated in the treatment of psoriasis vulgaris and better results were observed with the ointment formulation. Longer treatment courses could be advised.

钙化三醇软膏与乳膏治疗寻常型牛皮癣。
牛皮癣是一种多因素,慢性复发,炎症性皮肤病,发生在世界人口的1-3%。维生素D3类似物对银屑病皮损的增殖和分化以及中性粒细胞和免疫细胞的浸润和激活有影响。本研究旨在评估局部钙化三醇的疗效和安全性,并比较软膏和乳膏制剂治疗寻常型牛皮癣的疗效。共有41例轻至中度寻常型牛皮癣患者(18名男性和23名女性,年龄在5至63岁之间)被纳入研究。每位患者被指示在银屑病病灶上每天应用两次治疗。在治疗前和治疗结束时进行常规血液检查和血清钙检查。治疗评估在第2、4和6周进行,并基于银屑病面积和严重程度指数(PASI)评分。在我们研究的41例患者中,只有29例完成了疗程。治疗前PASI范围为1.2 - 43(平均值:12.1)。两组,50微克/克钙化三醇软膏(11例)和50微克/克钙化三醇乳膏(18例)均表现出时间依赖性改善,6周后出现极好的改善,总平均PASI从12.1显著降低到1.02。与乳膏组相比,软膏组的PASI显著降低(平均PASI分别从12.7降至0.8和11.1降至1.15)。除钙化三醇乳膏组少数患者出现轻度刺激外,两组均未见明显不良反应。综上所述,钙化三醇治疗寻常型银屑病有效、安全、耐受性好,且该软膏制剂疗效较好。建议延长疗程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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