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Eta 蛋白能否区分类风湿性关节炎和银屑病关节炎?

Does Eta Protein Differentiate Rheumatoid Arthritis from Psoriatic Arthritis?

机构信息

Department of Rheumatology, Aksaray Training and Research Hospital, Aksaray, Turkey.

Department of Rheumatology, Ankara Bilkent City Hospital, Ankara, Turkey.

出版信息

Curr Med Chem. 2024;31(39):6510-6520. doi: 10.2174/0109298673295359240422115759.

Abstract

AIM

The clinical symptoms and laboratory markers of Rheumatoid Arthritis (RA) and Psoriatic Arthritis (PsA) can be very similar, so making a differential diagnosis between these two diseases is often difficult. Serological parameters to be used in differential diagnosis can guide the clinician. This study aimed to investigate the usability of 14-3-3η (eta) protein as a biomarker in the differential diagnosis of PsA and RA, and the relationships between eta protein and disease activity scores and joint erosions in PsA and RA.

METHODS

54 PsA patients, 53 RA patients, and 56 healthy individuals were included in this study. The ELISA (Enzyme-Linked ImunoSorbent Assay) kit was used as a quantitative sandwich enzyme immunoassay technique to detect human eta protein levels. Receiver- operating Characteristic (ROC) curves analysis was used to determine the sensitivity and specificity of the eta protein.

RESULTS

Eta protein levels were found to be significantly higher in the RA group than in the PsA [B: -0.341, OR (95% CI): 0.711 (0.556-0.909), p: 0.007] and control [B: -0.225, OR (95% CI): 0.798 (0.641-0.995), p: 0.045] groups. Eta protein median values were significantly higher in patients with joint erosion than in those without [β= 0.151, OR (95% CI): 1.163 (1.003-1.349), p: 0.046].

CONCLUSION

Eta protein levels are higher in the serum of RA patients than PsA and are associated with joint erosion. Eta protein may be a potential biomarker in the differential diagnosis of RA and PsA. It may represent a possible therapeutic step in the pathophysiological pathways in the development of joint erosion.

摘要

目的

类风湿关节炎(RA)和银屑病关节炎(PsA)的临床症状和实验室标志物可能非常相似,因此这两种疾病的鉴别诊断往往很困难。用于鉴别诊断的血清学参数可以指导临床医生。本研究旨在探讨 14-3-3η(eta)蛋白作为鉴别诊断 PsA 和 RA 的生物标志物的可用性,以及 eta 蛋白与 PsA 和 RA 疾病活动评分和关节侵蚀之间的关系。

方法

本研究纳入了 54 例 PsA 患者、53 例 RA 患者和 56 名健康对照者。采用酶联免疫吸附试验(ELISA)试剂盒作为定量夹心酶免疫分析技术检测人 eta 蛋白水平。受试者工作特征(ROC)曲线分析用于确定 eta 蛋白的敏感性和特异性。

结果

RA 组 eta 蛋白水平明显高于 PsA [B:-0.341,OR(95%CI):0.711(0.556-0.909),p:0.007]和对照组 [B:-0.225,OR(95%CI):0.798(0.641-0.995),p:0.045]。有关节侵蚀的患者 eta 蛋白中位数明显高于无关节侵蚀的患者[β=0.151,OR(95%CI):1.163(1.003-1.349),p:0.046]。

结论

RA 患者血清中的 eta 蛋白水平高于 PsA,且与关节侵蚀有关。Eta 蛋白可能是 RA 和 PsA 鉴别诊断的潜在生物标志物。它可能代表了关节侵蚀发展的病理生理途径中的一个潜在治疗靶点。

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