Evaluating the Effects of Oral and Topical Simvastatin in the Treatment of Acne Vulgaris: A Double-blind, Randomized, Placebo-controlled Clinical Trial.

IF 3.2 Q2 Pharmacology, Toxicology and Pharmaceutics
Anahita Ahmadvand, Ameneh Yazdanfar, Fatemeh Yasrebifar, Younes Mohammadi, Reza Mahjub, Maryam Mehrpooya
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引用次数: 9

Abstract

Background: Acne vulgaris is a common dermatologic disorder which results in psychological consequences. Inflammatory responses play an important role in the development of inflammatory acne lesions. Recently, many studies have demonstrated anti-inflammatory effects of statins; thus, the aim of this study was to evaluate the efficacy of oral and topical Simvastatin as adjunct therapy in the treatment of acne vulgaris.

Methods: A total of 76 patients with moderate to very severe acne vulgaris, all receiving oral azithromycin (250 mg, 3 times a week, orally) and topical benzoyl peroxide gel (5%, once daily) were assigned to three groups: 1) Oral group received 20mg/day of oral simvastatin and blank solution, 2) Topical group received simvastatin 1% topical solution and oral placebo, 3) Placebo group received oral placebo and blank solution. The severity of acne was determined by global acne grading system (GAGS) at baseline and after 8 weeks of treatment.

Results: Comparing the three groups showed that topical simvastatin was associated with greater decrease in acne severity as compared with those of oral and placebo groups. Moreover, the oral simvastatin appeared to be more efficacious as compared with placebo group (P value<0.001). Oral and topical simvastatin were well tolerated in almost all patients.

Conclusion: Although preliminary, the results of this study showed that oral and topical statins, drugs with anti-inflammatory properties, can be considered as effective treatment for acne vulgaris as an adjunct to standard treatment. However, further studies with larger sample size, using improved formulations of topical simvastatin are needed to confirm these results.

评价口服和外用辛伐他汀治疗寻常痤疮的效果:一项双盲、随机、安慰剂对照的临床试验。
背景:寻常性痤疮是一种常见的皮肤病,可导致心理后果。炎症反应在炎症性痤疮病变的发展中起重要作用。最近,许多研究已经证明了他汀类药物的抗炎作用;因此,本研究的目的是评估口服和外用辛伐他汀作为辅助治疗寻常性痤疮的疗效。方法:将76例中重度寻常痤疮患者,均给予阿奇霉素口服(250 mg,每周3次,口服)和过氧化苯甲酯凝胶(5%,每日1次),分为3组:1)口服组给予辛伐他汀口服20mg/天,辛伐他汀1%外用溶液,辛伐他汀口服安慰剂,3)安慰剂组给予口服安慰剂,空白溶液。在基线和治疗8周后,通过全球痤疮分级系统(GAGS)确定痤疮的严重程度。结果:三组比较表明,与口服组和安慰剂组相比,局部辛伐他汀与痤疮严重程度的降低有关。此外,口服辛伐他汀组比安慰剂组更有效(P值)。结论:虽然初步研究结果表明,口服和外用他汀类具有抗炎特性的药物,作为标准治疗的辅助,可以被认为是治疗寻常痤疮的有效方法。然而,需要进一步研究更大的样本量,使用改进的局部辛伐他汀配方来证实这些结果。
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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来源期刊
Current clinical pharmacology
Current clinical pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
3.60
自引率
0.00%
发文量
0
期刊介绍: Current Clinical Pharmacology publishes frontier reviews on all the latest advances in clinical pharmacology. The journal"s aim is to publish the highest quality review articles in the field. Topics covered include: pharmacokinetics; therapeutic trials; adverse drug reactions; drug interactions; drug metabolism; pharmacoepidemiology; and drug development. The journal is essential reading for all researchers in clinical pharmacology.
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