评估局部硬皮病患者体内的硫醇二硫化物、缺血修饰白蛋白和 Prolidase 参数。

IF 2.5 4区 医学 Q2 DERMATOLOGY
Ayşe Akbaş, Orhan Şen, Fadime Kılınç, Salim Neşelioğlu, Gülhan Aksoy Saraç, Akın Aktaş
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引用次数: 0

摘要

简介:局限性硬皮病是一种罕见的炎症性皮肤病,引起真皮和皮下组织硬化。氧化应激可能在病因学中起作用,或对疾病的慢性或进展负责。目的:我们旨在通过检测硫醇-二硫平衡、缺血修饰白蛋白(IMA)和脯氨酸酶参数来研究局限性硬皮病患者氧化应激的存在。方法:选取20例18岁以上临床及病理诊断为局限性硬皮病的患者和20例对照组。询问并记录年龄、性别、发病年龄、病程以及是否伴有全身性疾病。通过皮肤病学检查计算病变类型及改良罗德曼评分和LoSSI评分。测量并比较患者组和对照组的CRP、沉降率、总硫醇、天然硫醇和二硫水平(由Erel谱、IMA水平和增殖酶水平指示)。结果:患者与对照组的天然硫醇(P=0.958)、总硫醇(P=0.979)、二硫(P=0.449)、二硫/天然硫醇% (P=0.368)、二硫/总硫醇% (P=0.361)、天然硫醇/总硫醇% (P=0.368)、增殖酶(P=0.121)水平相似。只有IMA有显著差异。天然硫醇、总硫醇、二硫、(二硫/天然硫醇)、(二硫/总硫醇)、IMA、增殖酶、Rodnan和LoSSI评分之间没有明显的关系。结论:根据本研究获得的数据,我们可以说,在局限性硬皮病中,硫醇-二硫平衡没有被破坏,增殖酶水平没有受到影响;然而,IMA受到负面影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Thiol Disulfide, Ischemia Modified Albumin, and Prolidase Parameters in Patients with Localized Scleroderma.

Introduction: Localized scleroderma is a rare inflammatory skin disease that causes sclerosis in the dermis and subcutaneous tissue. Oxidative stress may play a role in the etiology or be responsible for the chronicity or progression of the disease.

Objectives: We aimed to investigate the presence of oxidative stress in patients with localized scleroderma by examining thiol-disulfide balance, ischemia-modified albumin (IMA), and prolidase parameters.

Methods: Twenty patients over the age of 18 who were diagnosed with localized scleroderma both clinically and histopathologically and 20 control subjects were included in the study. Age, sex, age at disease onset, duration of the disease, and presence of accompanying systemic diseases were questioned and recorded. Lesion type and modified Rodnan and LoSSI scores were calculated through dermatological examination. CRP, sedimentation rate, total thiol, native thiol, and disulfide levels indicated by the Erel profile, IMA level, and prolidase levels were measured and compared in both the patient and control groups.

Results: Levels of native thiol (P=0.958), total thiol (P=0.979), disulfide (P=0.449), (disulfide/native thiol%) (P=0.368), (disulfide/total thiol%) (P=0.361), (native thiol/total thiol%) (P=0.368), and prolidase (P=0.121) were similar in both patient and control groups. Only IMA was significantly different. No significant relationship was found between the levels of native thiol, total thiol, disulfide, (disulfide/native thiol), (disulfide/total thiol), IMA, prolidase, and Rodnan and LoSSI scores.

Conclusion: According to the data obtained from this study, we can say that the thiol-disulfide balance is not disrupted and that prolidase levels are not affected in localized scleroderma; however, IMA is negatively affected.

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