钙保护蛋白水平作为斑秃患者新的炎症标志物。

Q3 Medicine
Hala M El-Sadek, Eman E Mohamed, Mona S Ali, Doaa A H Pessar, Fatima G Yehia, Basma E M Risha
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引用次数: 0

摘要

斑秃(AA)是一种炎症性、自身免疫性、非瘢痕性疾病。导致免疫特权丧失的确切机制尚不清楚。血清钙保护蛋白(CLP)水平是一些自身免疫性疾病的一个强大的预测因素和独特的炎症标志物。本研究旨在评估斑秃患者的CLP水平,并将其与疾病的各种临床特征(特别是严重程度)联系起来,以确定任何潜在的关联。本研究包括30名AA患者和30名年龄和性别匹配的志愿者作为对照。AA的严重程度根据脱发严重程度工具(SALT)评分确定。通过酶联免疫吸附试验测定所有参与者的血清CLP水平。AA患者血清CLP水平显著高于对照组(p < 0.0001)。CLP血清水平与患者年龄、SALT评分和病程有显著相关性(p=0.048, p < 0.0001和p < 0.0001)。此外,CLP水平与AA类型、严重程度和指甲影响之间存在显著关联(p < 0.0001, p < 0.0001和p=0.003)。综上所述,本研究结果表明AA与全身性炎症有关,CLP可能是AA患者炎症的有益指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum level of calprotectin as a new inflammatory marker in patients with alopacia areata.

Alopecia areata (AA) is an inflammatory and autoimmune, non-scarring condition. The exact mechanism that induces loss of immune privilege is unknown. Serum calprotectin (CLP) levels are a strong predictive factor and a unique inflammatory marker in several autoimmune disorders. This study aimed to evaluate CLP levels in alopecia areata patients and correlate them with various clinical characteristics of the disease, particularly severity, to identify any potential associations. The present study included 30 AA patients and 30 age and gender-matched volunteers as controls. Severity of AA was determined according to the Severity of Alopecia Tool (SALT) score. Serum CLP levels were measured in all participants by the Enzyme-Linked Immunosorbent Assay. The CLP serum levels were significantly higher in AA patients than in controls (p < 0.0001). A significant association was observed between CLP serum levels and age of patients, SALT score, and duration of disease (p=0.048, p < 0.0001 and p < 0.0001, respectively). Additionally, a significant association was present between CLP levels and type, severity of AA, and nail affection (p < 0.0001, p < 0.0001 and p=0.003, respectively). In conclusion, the present results demonstrated that AA was linked to systemic inflammation, and CLP could be a beneficial indicator of inflammation in AA patients.

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CiteScore
1.20
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0.00%
发文量
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