Second Department of Pediatrics, Aglaia Kyriakou University Hospital, National and Kapodistrian University of Athens, Athens, Greece -
Second Department of Pediatrics, Aglaia Kyriakou University Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Minerva Pediatr (Torino). 2023 Jun;75(3):395-399. doi: 10.23736/S2724-5276.17.04910-6. Epub 2017 Jun 22.
Cathelicidin has been correlated with the pathophysiology of atopic dermatitis (AD). An indirect correlation of vitamin D with the course of the disease has already been reported as it directly affects the levels of cathelicidin. The purpose of the present article is to investigate the impact of vitamin D supplementation on the course of AD.
We conducted a prospective observational study. The severity of AD was assessed with the clinical tool SCORAD (SCORing Atopic Dermatitis) which is developed by the European Task Force on AD.
Fifty children with AD were enrolled and stratified in two groups based on the severity of SCORAD. Children with severe AD (SCORAD Index >40) received higher doses of vitamin D in order to sufficiently reduce the disease (comparable SCORAD Index for children with mild atopic dermatitis). While the baseline SCORAD differed statistically significant level between the two groups of children with AD (P<0.001) this difference disappeared at 20 (P=0.649) days and remained statistically insignificant both at 45 days (P=0.610), and at the end of the administration of treatment (P=0.474). This effect was based on a significant downregulation of the severity of symptoms in the group of children that received 2400 IU of vitamin D.
The findings of our study suggest that vitamin D may be accurately used in current clinical practice for the management of AD. However, the recommended dose should be titrated taking in mind the severity of the disease.
抗菌肽与特应性皮炎(AD)的病理生理学有关。已经有报道称,维生素 D 与疾病的发生呈间接相关,因为它直接影响抗菌肽的水平。本文旨在探讨维生素 D 补充对 AD 病程的影响。
我们进行了一项前瞻性观察性研究。AD 的严重程度使用 SCORAD(特应性皮炎评分)这一临床工具进行评估,该工具由欧洲 AD 工作组开发。
共纳入 50 例 AD 患儿,并根据 SCORAD 的严重程度分为两组。严重 AD 患儿(SCORAD 指数>40)接受较高剂量的维生素 D,以充分降低疾病严重程度(与轻度特应性皮炎患儿的 SCORAD 指数相当)。虽然两组 AD 患儿的基线 SCORAD 存在统计学显著差异(P<0.001),但在 20 天(P=0.649)、45 天(P=0.610)和治疗结束时(P=0.474),这一差异消失。这一效果基于接受 2400IU 维生素 D 治疗的患儿症状严重程度显著降低。
本研究结果表明,维生素 D 可能可在当前临床实践中准确用于 AD 的管理。然而,应根据疾病的严重程度来调整推荐剂量。