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肿瘤坏死因子-α刺激基因-6:反映类风湿关节炎疾病活动的生物标志物。

Tumor necrosis factor-alpha stimulated gene-6: A biomarker reflecting disease activity in rheumatoid arthritis.

机构信息

Department of Clinical Laboratory, The Second Affiliated Hospital of Nanchang University, Nanchang, China.

Jiangxi Province Key Laboratory of Laboratory Medicine, Nanchang, China.

出版信息

J Clin Lab Anal. 2022 May;36(5):e24395. doi: 10.1002/jcla.24395. Epub 2022 Mar 30.

DOI:10.1002/jcla.24395
PMID:35353944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9102767/
Abstract

BACKGROUND

To explore the serum tumor necrosis factor-alpha stimulated gene-6 (TSG-6) level and its association with disease activity in rheumatoid arthritis (RA) patients.

METHODS

We recruited 176 RA patients, 178 non-RA patients (lupus erythematosus, osteoarthritis, ulcerative colitis, ankylosing spondylitis and psoriasis) and 71 healthy subjects. Serum TSG-6 levels were detected by enzyme-linked immunosorbent assay (ELISA). RA patients were divided into inactive RA and active RA groups by disease activity score of 28 joints based on C-reactive protein (DAS28-CRP). The receiver operating characteristic (ROC) curve and Spearman's rank correlation test analyzed the correlation between TSG-6 concentration and RA disease activity.

RESULTS

Tumor necrosis factor-alpha stimulated gene-6 levels in the RA group were increased (p < 0.01). TSG-6 concentrations indicated an upward tendency with increased disease activity; The area under the curve (AUC) of TSG-6 for diagnosing RA and assessing the severity of RA were 0.78 and 0.80, respectively; The combination of TSG-6 and anti-mutated citrullinated vimentin antibodies (anti-MCV) (sensitivity:98.4%)improved the diagnostic accuracy of RA. Binary logistic regression analysis showed that TSG-6 was an independent risk factor related to the severity of RA, and OR (95% CI) was 1.2 (1.003-1.453).

CONCLUSION

The TSG-6 levels in RA patients were elevated and related to disease activity. Therefore, TSG-6 may serve as a new potential biomarker for evaluating RA disease activity.

摘要

背景

探讨类风湿关节炎(RA)患者血清肿瘤坏死因子-α刺激基因-6(TSG-6)水平及其与疾病活动度的关系。

方法

招募了 176 例 RA 患者、178 例非 RA 患者(狼疮、骨关节炎、溃疡性结肠炎、强直性脊柱炎和银屑病)和 71 例健康对照者。采用酶联免疫吸附试验(ELISA)检测血清 TSG-6 水平。根据 C 反应蛋白(DAS28-CRP)计算的 28 关节疾病活动评分(DAS28)将 RA 患者分为活动期 RA 组和缓解期 RA 组。通过受试者工作特征(ROC)曲线和斯皮尔曼等级相关检验分析 TSG-6 浓度与 RA 疾病活动度的相关性。

结果

RA 组 TNF-α刺激基因-6(TSG-6)水平升高(p<0.01)。TSG-6 浓度随着疾病活动度的增加呈上升趋势;TSG-6 诊断 RA 和评估 RA 严重程度的曲线下面积(AUC)分别为 0.78 和 0.80;TSG-6 与抗突变型瓜氨酸波形蛋白抗体(anti-MCV)联合(敏感度:98.4%)提高了 RA 的诊断准确性。二元逻辑回归分析显示,TSG-6 是与 RA 严重程度相关的独立危险因素,OR(95%CI)为 1.2(1.003-1.453)。

结论

RA 患者 TSG-6 水平升高,与疾病活动度相关。因此,TSG-6 可能成为评估 RA 疾病活动度的新的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae69/9102767/590a40807313/JCLA-36-e24395-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae69/9102767/fec60c26a25e/JCLA-36-e24395-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae69/9102767/8395991fe8c3/JCLA-36-e24395-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae69/9102767/590a40807313/JCLA-36-e24395-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae69/9102767/fec60c26a25e/JCLA-36-e24395-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae69/9102767/8395991fe8c3/JCLA-36-e24395-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae69/9102767/590a40807313/JCLA-36-e24395-g001.jpg

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