Combined use of Serum miR-338-3p, Cartilage Oligomeric Matrix Protein and Chondroitin Sulfate-846 in the Early Diagnosis of Knee Osteoarthritis

被引:9
|
作者
Dou, Xiaojie [1 ]
Zhang, Zhaodong [1 ]
Wang, Shuai [2 ]
Zhou, Xuemei [3 ]
机构
[1] Dalian Univ, Dept Orthoped, Affiliated Zhongshan Hosp, Jiefang St 6, Dalian 116001, Liaoning, Peoples R China
[2] Binzhou Peoples Hosp, Dept Orthoped, Binzhou, Shandong, Peoples R China
[3] Dalian Childrens Hosp, Dept Pediat, Dalian, Liaoning, Peoples R China
关键词
miR-338-3p; cartilage oligomeric matrix protein; chondroitin sulfate-846; knee osteoarthritis; BIOMARKER; COMP;
D O I
10.7754/Clin.Lab.2018.180803
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: In this study, the serum levels of miR-338-3p, COMP, and CS-846 were detected in the patients with KOA and healthy controls, to explore the value of miR-338-3p, COMP, and CS-846 in the early diagnosis of KOA. Methods: Real-time PCR was carried out to evaluate the level of miR-338-3p in KOA patients and healthy controls. Spearman's correlation coefficient was performed to examine the correlation between the expression of miR-338-3p, COMP, and CS-846. Receiver operating characteristic (ROC) curves were carried out to evaluate the diagnostic values of miR-338-3p, COMP, and CS-846 for KOA patients. Results: In the current study, we first demonstrated that serum miR-338-3p, COMP, and CS-846 levels were increased in KOA patients compared to healthy controls. Moreover, the increase of miR-338-3p, COMP, and CS846 levels positively correlated with VAS scores and joint space narrowing, suggesting miR-338-3p positively correlated with comprehensive disease severity. In addition, miR-338-3p, COMP, and CS-846 could be used as an independent biomarker for KOA patients. More importantly, combined use of miR-338-3p, COMP, and CS-846 demonstrates a higher diagnostic value with an AUC 0.926 for KOA patients. Conclusions: The combination of miR-338-3p, COMP, and CS-846 demonstrated higher diagnostic value for KOA patients, indicating their combination as novel and promising biomarkers for diagnosis and disease severity of KOA.
引用
收藏
页码:319 / 324
页数:6
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