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首页> 外文期刊>Annals of Dermatology >Clinical Relevance for Serum Cold-Inducible RNA-Binding Protein Level in Alopecia Areata
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Clinical Relevance for Serum Cold-Inducible RNA-Binding Protein Level in Alopecia Areata

机译:脱发症患者血清冷诱导RNA结合蛋白水平的临床意义

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Background Alopecia areata (AA), a chronic, relapsing hair-loss disorder, is considered to be a T-cell-mediated autoimmune disease. Cold-inducible RNA-binding protein (CIRP) belongs to a family of cold-shock proteins that respond to cold stress, and has been identified as a damage-associated molecular pattern (DAMP) molecule that triggers the inflammatory response. Recent studies have shown that high-mobility group box 1, another DAMP molecule, is elevated in serum and scalp tissue of AA patients, suggesting a relationship between DAMP molecules and the pathogenesis of AA. Objective To investigate the clinical significance of serum CIRP levels in AA. Methods The serum levels of CIRP were compared between 68 patients with AA and 20 healthy controls. Additionally, the correlation between CIRP level and various clinical parameters was evaluated. Results The serum CIRP levels were significantly higher in AA patients compared to healthy subjects. Moreover, there was an association between the serum CIRP level and clinical characteristics, such as disease duration and disease activity. However, there was no significant difference in the serum CIRP level among the clinical types of AA (AA multiplex, alopecia totalis, and alopecia universalis). Conclusion These results suggest that CIRP may play a significant role in the pathogenesis of AA and could be a potential biologic marker for monitoring the disease activity of AA.
机译:背景斑秃(AA)是一种慢性复发性脱发疾病,被认为是T细胞介导的自身免疫性疾病。冷诱导RNA结合蛋白(CIRP)属于一种冷休克蛋白家族,可响应冷应激,并且已被鉴定为触发炎症反应的损伤相关分子模式(DAMP)分子。最近的研究表明,AA病人的血清和头皮组织中的另一种DAMP分子高迁移率族框1升高,表明DAMP分子与AA的发病机理之间存在关联。目的探讨AA患者血清CIRP水平的临床意义。方法比较68例AA患者和20例健康对照者的CIRP血清水平。此外,还评估了CIRP水平与各种临床参数之间的相关性。结果与健康受试者相比,AA患者的血清CIRP水平显着更高。此外,血清CIRP水平与临床特征(如疾病持续时间和疾病活动)之间存在关联。但是,在AA的临床类型(AA多重性,总秃发和通用性秃发)之间,血清CIRP水平没有显着差异。结论这些结果表明CIRP在AA的发病机制中可能起着重要作用,并且可能是监测AA疾病活动的潜在生物学标记。

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