首页> 美国卫生研究院文献>Springer Open Choice >Topical Ivermectin 10 mg/g and Oral Doxycycline 40 mg Modified-Release: Current Evidence on the Complementary Use of Anti-Inflammatory Rosacea Treatments
【2h】

Topical Ivermectin 10 mg/g and Oral Doxycycline 40 mg Modified-Release: Current Evidence on the Complementary Use of Anti-Inflammatory Rosacea Treatments

机译:伊维菌素局部10毫克/克和口服强力霉素40毫克改良释放:辅助使用抗炎性酒渣鼻治疗的最新证据

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Rosacea is a common, chronic inflammatory skin disease that can present with a variety of signs and symptoms. The potentially simultaneous occurrence of different signs and symptoms is due to different underlying inflammatory pathways, emphasizing the need for complementary treatment approaches. Topical ivermectin cream (10 mg/g) and systemic, oral anti-inflammatory doxycycline (40 mg modified-release) are both approved for the treatment of papulopustular rosacea (PPR). Whether or not a combined therapeutic approach may be more beneficial than monotherapy for patients with PPR remains to be tested. Here, we summarize underlying inflammatory pathways implicated in rosacea and clarify the impact of these two agents on selective pathways during inflammation, due to specific characteristics of their individual mechanisms of action (MoA). Based on the complementary MoA of doxycycline modified-release and ivermectin, a scientific rationale for a combined therapy targeting inflammatory lesions in rosacea is given. We propose that topical ivermectin cream is a promising new candidate as first-line treatment to target the inflammatory lesions of rosacea, which can be used in combination with systemic doxycycline modified-release to provide an optimal treatment approach considering all inflammatory pathways involved in PPR.>Funding Galderma.
机译:酒渣鼻是一种常见的慢性炎症性皮肤病,可表现出各种体征和症状。不同体征和症状可能同时发生是由于不同的潜在炎症途径,从而强调了对补充治疗方法的需求。局部用伊维菌素乳膏(10 mg / g)和全身性口服抗炎多西环素(40 mg缓释)均被批准用于乳头脓疱性酒渣鼻(PPR)的治疗。对于PPR患者,联合治疗是否比单药治疗更有益尚待检验。在这里,我们总结了与酒渣鼻有关的潜在炎症途径,并阐明了这两种药物在炎症过程中对选择性途径的影响,这归因于它们各自的作用机制(MoA)的特定特征。基于强力霉素缓释和伊维菌素的互补MoA,给出了针对酒渣鼻炎性病变的联合治疗的科学依据。我们建议局部用伊维菌素乳膏作为靶向治疗酒渣鼻炎性病变的一线治疗药物是有希望的新候选药物,考虑到参与PPR的所有炎性途径,可将其与全身强力霉素缓释剂联合使用以提供最佳治疗方法。 >资金

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号