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解偶联蛋白1(UCP1)水平与银屑病之间的关系。

Relationship between uncoupling protein 1 (UCP1) levels and psoriasis.

作者信息

Akyürek Fikret, Tuncez Akyürek Fatma, Şengül Bağ Fatma

机构信息

Department of Medical Biochemistry, Faculty of Medicine, Selçuk University, Konya, Turkiye.

Department of Dermatology, Faculty of Medicine, Selçuk University, Konya, Turkiye.

出版信息

Turk J Med Sci. 2024 Dec 30;55(1):215-222. doi: 10.55730/1300-0144.5960. eCollection 2025.

Abstract

BACKGROUND/AIM: Psoriasis is a common chronic autoimmune skin disease. Comorbidities increase the mortality risk of the disease. The aim of this study was to investigate the changes in uncoupling protein 1 (UCP1) level in psoriasis patients and evaluate its possible role in the pathogenesis of the disease, focusing on disease severity (Psoriasis Area and Severity Index), dyslipidemia, inflammation, and cardiovascular risk.

MATERIALS AND METHODS

This study included 30 psoriasis patients and 30 healthy individuals as a control group. Serum UCP1 was measured using an ELISA test kit. The laboratory results of psoriasis patients and healthy controls were compared.

RESULTS

UCP1 level was a significant candidate marker for the prediction of psoriatic disease (AUC: 0.708, 95% CI: 0.577-0.819, p = 0.002) with sensitivity of 66.67%, specificity of 76.67%, negative predictive value of 69.7%, and positive predictive value of 74.1%. Simple logistic regression analysis showed that an individual with a UCP1 value below 7.561 had a 73% lower probability (OR: 0.27, 95% CI: 0.08-0.94, p = 0.039) of developing psoriasis than an individual with a UCP1 value above 7.561. Among the biochemical parameters, the high-sensitivity C-reactive protein and triglyceride levels of the patients were significantly higher compared to those of the healthy controls while their high-density lipoprotein levels were lower.

CONCLUSION

According to the sensitivity (66.67%) and specificity (76.67%) of UCP1, it may be a valuable candidate marker in the diagnosis of psoriasis patients in symptomatic and asymptomatic phases. Further work is needed to substantiate these findings.

摘要

背景/目的:银屑病是一种常见的慢性自身免疫性皮肤病。合并症会增加该疾病的死亡风险。本研究旨在调查银屑病患者中解偶联蛋白1(UCP1)水平的变化,并评估其在疾病发病机制中的可能作用,重点关注疾病严重程度(银屑病面积和严重程度指数)、血脂异常、炎症和心血管风险。

材料与方法

本研究纳入30例银屑病患者和30名健康个体作为对照组。使用酶联免疫吸附测定(ELISA)试剂盒检测血清UCP1。比较银屑病患者和健康对照的实验室结果。

结果

UCP1水平是预测银屑病的重要候选标志物(曲线下面积:0.708,95%置信区间:0.577 - 0.819,p = 0.002),敏感性为66.67%,特异性为76.67%,阴性预测值为69.7%,阳性预测值为74.1%。简单逻辑回归分析显示,UCP1值低于7.561的个体患银屑病的概率比UCP1值高于7.561的个体低73%(比值比:0.27,95%置信区间:0.08 - 0.94,p = 0.039)。在生化参数方面,患者的高敏C反应蛋白和甘油三酯水平显著高于健康对照,而高密度脂蛋白水平较低。

结论

根据UCP1的敏感性(66.67%)和特异性(76.67%),它可能是银屑病患者有症状和无症状阶段诊断中有价值的候选标志物。需要进一步开展工作来证实这些发现。

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