Evaluation of synovial inflammation in juvenile idiopathic arthritis using superb microvascular imaging compared with power Doppler ultrasound

被引:3
|
作者
Sun, P. [1 ]
Tong, Y. [2 ]
Xu, X. [1 ]
Gao, M. [1 ]
Shi, J. [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Childrens Med Ctr, Diagnost Imaging Ctr, Sch Med, 1678 Dongfang Rd, Shanghai 200127, Peoples R China
[2] Fudan Univ, Shanghai Canc Ctr, Shanghai Med Coll, Dept Ultrasound, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
juvenile idiopathic arthritis; ultrasound; power Doppler; superb microvascular imaging; prognosis; DISEASE-ACTIVITY SCORE; REMISSION; CHILDREN;
D O I
10.55563/clinexprheumatol/ksl2uy
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective This study aimed to investigate the diagnostic and prognostic performance of superb microvascular imaging (SMI) in evaluation of synovial inflammation in patients with juvenile idiopathic arthritis (JIA) compared with power Doppler ultrasound (PDUS). Methods Fifty-nine patients with active disease and 62 patients with inactive disease were enrolled. The synovial inflammation was evaluated via vascularity index (VI) of SMI and PDUS. The correlations between VIs and the inflammatory biomarkers were analysed by Spearman's coefficient. Receiver operating characteristics curves were plotted to examine the prognostic value of SMI and PDUS. Results The VI of SMI was significantly higher than that of PDUS in JIA patients regardless of the disease activity. The SMI and PDUS VI were significantly correlated with levels of erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and serum amyloid A (SAA). The SMI VI was significantly higher in patients with relapse than in those with remission, and showed superior performance in predicting relapse in JIA patients with inactive disease. Conclusion SMI may detect the synovial inflammation with greater sensitivity than PDUS in patients with JIA, and correlate well with the inflammatory biomarkers. SMI signal in the knees might play an important role in prediction of relapse in clinically inactive patients, thus allowing personalised treatment strategies for JIA patients.
引用
收藏
页码:1127 / 1134
页数:8
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