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儿童慢性自发性荨麻疹患者的血浆脂氧素A4水平

Plasma lipoxin A4 levels in childhood chronic spontaneous urticaria.

作者信息

Dilek Fatih, Özçeker Deniz, Güler Eray Metin, Özkaya Emin, Yazıcı Mebrure, Tamay Zeynep, Koçyiğit Abdurrahim, Güler Nermin

机构信息

Department of Pediatric Allergy and Immunology, University of Health Sciences, Kayseri Training and Research Hospital, Kayseri, Turkey.

Department of Pediatric Allergy, University of Health Sciences, Okmeydanı Training and Research Hospital, İstanbul, Turkey.

出版信息

Turk J Pediatr. 2018;60(5):527-534. doi: 10.24953/turkjped.2018.05.009.

Abstract

Dilek F, Özçeker D, Güler EM, Özkaya E, Yazıcı M, Tamay Z, Koçyiğit A, Güler N. Plasma lipoxin A4 levels in childhood chronic spontaneous urticaria. Turk J Pediatr 2018; 60: 527-534. Chronic spontaneous urticaria (CSU) is an idiopathic inflammatory disorder. Despite great research progress, the pathogenesis of the disease is still not fully understood. Lipoxins (LXs) are autacoid lipid metabolites that are the first discovered members of a new genus named called specialized proresolving mediators. In this study, we aimed to investigate the possible role of LXA4 in the pathogenesis of CSU. Forty-two children with CSU and 25 healthy children were enrolled in the study. The demographic and clinical features of patients were evaluated, autologous serum skin tests (ASSTs), and routine laboratory assessments were performed. Disease activity was determined using the urticaria activity score. An enzyme-linked immunosorbent assay was used to evaluate LXA4 plasma levels. The median value of plasma LXA4 was found to be 60.8 ng/ml (interquartile range, 48.1-71.8) in CSU patients and 137.4 ng/ml (121.4-150.8) in the control group. The difference between the groups was statistically significant (p < 0.001). Additionally, the median plasma LXA4 levels in the ASST-positive patients were significantly reduced compared to the ASST-negative ones (45.8 [36.7-67.6] versus 63.8 [58.3-78.9] ng/ml, respectively, p < 0.05). Our results showed that diminished LXA4 biosynthesis may be a critical part of CSU pathogenesis in children, especially in patients with an autoimmune component.

摘要

迪莱克·F、厄兹切克·D、居勒·E·M、厄兹卡亚·E、亚齐奇·M、塔迈·Z、科奇伊吉特·A、居勒·N。儿童慢性自发性荨麻疹患者血浆脂氧素A4水平。《土耳其儿科学杂志》2018年;60:527 - 534。慢性自发性荨麻疹(CSU)是一种特发性炎症性疾病。尽管研究取得了很大进展,但该疾病的发病机制仍未完全阐明。脂氧素(LXs)是自分泌脂质代谢产物,是名为“特殊促消退介质”的新一类物质中最早被发现的成员。在本研究中,我们旨在探讨LXA4在CSU发病机制中的可能作用。42例CSU患儿和25例健康儿童纳入研究。评估患者的人口统计学和临床特征,进行自体血清皮肤试验(ASSTs)和常规实验室检查。使用荨麻疹活动评分确定疾病活动度。采用酶联免疫吸附测定法评估血浆LXA4水平。CSU患者血浆LXA4的中位数为60.8 ng/ml(四分位间距,48.1 - 71.8),对照组为137.4 ng/ml(121.4 - 150.8)。两组间差异有统计学意义(p < 0.001)。此外,ASST阳性患者的血浆LXA4中位数水平显著低于ASST阴性患者(分别为45.8 [36.7 - 67.6]与63.8 [58.3 - 78.9] ng/ml,p < 0.05)。我们的结果表明,LXA4生物合成减少可能是儿童CSU发病机制的关键部分,尤其是在有自身免疫成分的患者中。

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