Pediatric Dermatology Unit, First Department of Pediatrics, National and Kapodistrian University of Athens, "Aghia Sophia" Children's Hospital, Athens, Greece.
Pediatric Department, Kingston Hospital, London, UK.
Pediatr Dermatol. 2023 Jan;40(1):78-83. doi: 10.1111/pde.15117. Epub 2022 Aug 29.
Ectoine is a widespread osmolyte enabling halophilic bacteria to withstand high osmotic stress that has many potential applications ranging from cosmetics to its use as a therapeutic agent.
The aim of this study was to compare the efficacy and tolerability of ectoine 1% and hyaluronic acid 0.1% containing (EHA) cream with a vehicle cream in children with mild-to-moderate atopic dermatitis (AD).
A randomized, controlled, observer-blind, multicenter clinical trial was conducted in children aged 2-18 years, diagnosed with mild-to-moderate AD (SCORAD ≤20). Patients were randomized to either receiving EHA cream or vehicle cream twice daily for 4 weeks. The primary outcome measure was the mean change in objective SCORAD from baseline to the final visit. The secondary outcome measures included the mean change in Investigator's Global Assessment score, patient's judgment of efficacy and patient's assessment of pruritus. Safety of EHA cream was also assessed.
A total of 70 patients (35 in each group) were randomized and 57 were included in the final analysis set. Based on SCORAD measurements, patients using EHA cream achieved superior clinical improvement compared to the control group at 28 days (p < .001). EHA cream was also superior to the vehicle cream regarding all secondary outcome measures. Eight (23.5%) patients receiving EHA cream and two (5.7%) patients receiving vehicle cream experienced mild cutaneous adverse events (AEs).
In children 2-18 years old with mild-to-moderate AD, EHA cream was superior to vehicle cream, with minor AEs.
海藻糖是一种广泛存在的渗透调节剂,使嗜盐细菌能够耐受高渗透压,在化妆品等领域有许多潜在的应用,也可用作治疗剂。
本研究旨在比较 1%海藻糖和 0.1%透明质酸(EHA)乳膏与赋形剂乳膏在 2-18 岁轻中度特应性皮炎(AD)儿童中的疗效和耐受性。
在 2-18 岁患有轻中度 AD(SCORAD≤20)的儿童中进行了一项随机、对照、观察者盲、多中心临床试验。患者随机接受 EHA 乳膏或赋形剂乳膏,每天两次,持续 4 周。主要终点是从基线到最终访视时客观 SCORAD 的平均变化。次要终点包括研究者整体评估评分、患者对疗效的判断和患者对瘙痒的评估的平均变化。还评估了 EHA 乳膏的安全性。
共有 70 名患者(每组 35 名)随机分组,57 名患者纳入最终分析集。根据 SCORAD 测量结果,使用 EHA 乳膏的患者在 28 天时临床改善优于对照组(p<0.001)。EHA 乳膏在所有次要终点上也优于赋形剂乳膏。接受 EHA 乳膏治疗的 8 名(23.5%)患者和接受赋形剂乳膏治疗的 2 名(5.7%)患者出现轻度皮肤不良事件(AE)。
在 2-18 岁轻中度 AD 儿童中,EHA 乳膏优于赋形剂乳膏,不良反应轻微。