Eke Gungor Hatice, Sahiner Umit Murat, Karakukcu Cigdem, Sahiner Neriman, Altuner Torun Yasemin
Kayseri Education and Research Hospital, Department of Pediatrics, Pediatric Allergy and Immunology Unit, 38010 Erkilet, Kayseri, Turkey.
Kayseri Education and Research Hospital, Department of Biochemistry, 38010 Erkilet, Kayseri, Turkey.
Allergol Immunopathol (Madr). 2016 May-Jun;44(3):221-5. doi: 10.1016/j.aller.2015.05.005. Epub 2015 Aug 28.
Gelsolin is an actin-binding protein with several cellular functions including anti-apoptosis and is reported to have an anti-inflammatory effect. Apoptosis of keratinocytes has been implicated as a key mechanism of atopic dermatitis (AD).
We aimed to determine plasma gelsolin (pGSN) levels in children with atopic dermatitis (AD).
The diagnosis of AD was made according to Hanifin and Rajka criteria. The disease severity was scored by objective SCORAD index by the same allergist. Skin prick testing (SPT), total IgE levels, and eosinophil counts were analyzed. The pGSN levels were determined using ELISA technique.
Children aged between 0.5 and 3.0 years were included in the study. The children with AD (AD; n=84) were analyzed in two groups according to the presence (AD+/Atopy+; n=54) or absence of SPT positivity (AD+/Atopy-; n=30). The comparisons were made with a healthy control group matched for age and sex (n=81). The median (interquartile range) of pGSN levels in AD+/A+, AD+/A- and control groups were 267μg/ml (236-368), 293 (240-498) and 547 (361-695), respectively (p<0.001). The difference between the control group and AD sub-groups remained significant after Bonferroni correction (p<0.001). Correlation analysis failed to reach significance with the disease severity total IgE levels and eosinophil counts.
This is the first study investigating the association of pGSN levels with AD and disease severity. pGSN levels decreased in AD. These findings suggest that gelsolin may have a role in the disease process in AD patients.
凝溶胶蛋白是一种肌动蛋白结合蛋白,具有多种细胞功能,包括抗凋亡作用,据报道还具有抗炎作用。角质形成细胞凋亡被认为是特应性皮炎(AD)的关键机制。
我们旨在测定特应性皮炎(AD)患儿的血浆凝溶胶蛋白(pGSN)水平。
根据Hanifin和Rajka标准诊断AD。由同一位过敏症专科医生使用客观SCORAD指数对疾病严重程度进行评分。分析皮肤点刺试验(SPT)、总IgE水平和嗜酸性粒细胞计数。使用ELISA技术测定pGSN水平。
年龄在0.5至3.0岁之间的儿童纳入研究。AD患儿(AD;n = 84)根据SPT阳性(AD+/特应性体质+;n = 54)或阴性(AD+/特应性体质-;n = 30)分为两组。与年龄和性别匹配的健康对照组(n = 81)进行比较。AD+/A+组、AD+/A-组和对照组的pGSN水平中位数(四分位间距)分别为267μg/ml(236 - 368)、293(240 - 498)和547(361 - 695)(p<0.001)。经Bonferroni校正后,对照组与AD亚组之间的差异仍具有显著性(p<0.001)。相关性分析未发现与疾病严重程度、总IgE水平和嗜酸性粒细胞计数有显著相关性。
这是第一项研究pGSN水平与AD及疾病严重程度之间关联的研究。AD患者的pGSN水平降低。这些发现表明凝溶胶蛋白可能在AD患者的疾病进程中起作用。