Department of Child Health and Diseases, Health Sciences University, Dr. Sami Ulus Maternity and Children's Health and Diseases Training and Research Hospital, Ankara, 06080, Turkey.
Department of Child Health and Diseases, Division of Pediatric Immunology and Allergy, Health Sciences University, Gülhane Education and Research Hospital, Ankara, 06010, Turkey.
Arch Dermatol Res. 2020 Dec;312(10):697-703. doi: 10.1007/s00403-020-02054-5. Epub 2020 Mar 11.
Atopic dermatitis (AD) is a chronic disease of infancy and its pathogenesis remains unclear. There are recent studies suggesting that oxidative stress could play a role in the pathophysiology of atopic dermatitis. The aim of this study was to evaluate thiol (SH)-disulfide (SS) hemostasis as a new marker of oxidative stress (OS) in infants with atopic dermatitis. Thirty-one infants with AD and 30 healthy infants were included in a prospective, cross-sectional study. PO-SCORAD Index of infants with atopic dermatitis was calculated at the time of sample collection. Total antioxidant status (TAS), total oxidant status (TOS), native thiol (-SH), total thiol (-SH + -S-S-), and disulfide (SS) were measured in the control and patient groups. SS/SH, SS/total SH, SH/total SH ratios were compared between the groups. Mean native thiol and total thiol concentrations of the patient group were lower than the control group (p = 0.012; 0.047). The mean disulfide concentration of the patient group was significantly higher than the control group (p = 0.025). SS/SH, SS/total SH, and SH/total SH ratios were significantly higher in the patient group than in the control group (p < 0.05). There was a positive correlation between the duration of the breasting of the patients and thiol concentrations (p = 0.000). In our study, we found increased oxidative stress and decreased antioxidant defense mechanisms in infants with AD. Dynamic thiol-disulfide balance in the patient group was weakened and the balance shifted towards the oxidative side. These results may shed light on etiopathogenesis of atopic dermatitis and be useful in the development of new therapeutic methods.
特应性皮炎(AD)是一种婴幼儿期的慢性疾病,其发病机制尚不清楚。最近的研究表明,氧化应激可能在特应性皮炎的病理生理学中起作用。本研究旨在评估硫醇(SH)-二硫键(SS)止血作为特应性皮炎患儿氧化应激(OS)的新标志物。将 31 名特应性皮炎患儿和 30 名健康婴儿纳入前瞻性、横断面研究。在采集样本时计算特应性皮炎患儿的 PO-SCORAD 指数。在对照组和患者组中测量总抗氧化状态(TAS)、总氧化状态(TOS)、天然硫醇(-SH)、总硫醇(-SH+ -S-S-)和二硫键(SS)。比较两组之间 SS/SH、SS/总 SH 和 SH/总 SH 比值。患者组的平均天然硫醇和总硫醇浓度低于对照组(p=0.012;0.047)。患者组的平均二硫键浓度明显高于对照组(p=0.025)。患者组的 SS/SH、SS/总 SH 和 SH/总 SH 比值明显高于对照组(p<0.05)。患者的母乳喂养时间与硫醇浓度呈正相关(p=0.000)。在我们的研究中,我们发现 AD 患儿存在氧化应激增加和抗氧化防御机制减弱。患者组的硫醇-二硫键动态平衡减弱,平衡向氧化侧转移。这些结果可能有助于阐明特应性皮炎的发病机制,并有助于开发新的治疗方法。