Choate Evan A, Kaeley Gurjit S, Brook Jenny, Altman Roy D, FitzGerald John D, Floegel-Shetty Astrid R, Elashoff David A, Ranganath Veena K
1Department of Medicine, Division of Rheumatology, University of California, Los Angeles, CA USA.
2College of Medicine, University of Florida, Jacksonville, Florida USA.
BMC Rheumatol. 2020 Feb 3;4:8. doi: 10.1186/s41927-019-0107-2. eCollection 2020.
Joint replacements continue to occur during a rheumatoid arthritis (RA) patient's lifetime despite significant advances in available treatment options. The purpose of this study was to examine and quantify synovitis in surgically operated joints by ultrasound (US) in RA patients starting a new therapeutic agent.
RA subjects were enrolled in either tocilizumab or tofacitinib open-label, investigator-initiated trials and were assessed by ultrasound. In a subset of RA patients with joint replacements and/or operations of joint areas (OJA; e.g. joint arthroscopies, fusions, and synovectomies), joint-level scores of synovitis were compared between replaced joints, OJAs, and native joints. Joint-level synovitis was measured by grayscale (GSUS (0-3)) and power Doppler (PDUS (0-3)) at baseline and follow-up (3-6 months). McNemar's test or Wilcoxon signed rank test utilized the mixed effects ordinal logistic regression models.
Twenty RA patients had a total of 25 replaced joints and 24 OJA. All replaced joints had GSUS> 1 and 92% had PDUS> 1 at baseline, while OJA and native joints had lower evidence of GSUS> 1 (37.5, 38% respectively) and PDUS> 1 (45.8, 62% respectively). GSUS and PDUS semiquantitative scores improved significantly with treatment in replaced joints ( = 0.01, = 0.007), and native joints ( < 0.001 both), but not OJA.
In RA, joint replacement does not eliminate or prevent ultrasound measured synovitis, where all replaced joints have some evidence of US synovitis. US can also act as a potential marker of response to therapy in replaced joints. Scoring US synovitis in replaced joints should be considered in ultrasound RA clinical trials.
ClinicalTrials.gov NCT01717859 (registered 10/31/2012); ClinicalTrials.gov NCT02321930 (registered 12/22/2014).
尽管现有治疗方案取得了重大进展,但类风湿性关节炎(RA)患者一生中仍会持续进行关节置换。本研究的目的是通过超声(US)检查并量化开始使用新治疗药物的RA患者手术关节中的滑膜炎。
RA受试者参加了托珠单抗或托法替布的开放标签、研究者发起的试验,并接受了超声评估。在一部分进行过关节置换和/或关节区域手术(OJA;如关节镜检查、融合术和滑膜切除术)的RA患者中,比较了置换关节、OJA和天然关节之间的滑膜炎关节水平评分。在基线和随访(3 - 6个月)时,通过灰阶(GSUS(0 - 3))和能量多普勒(PDUS(0 - 3))测量关节水平的滑膜炎。McNemar检验或Wilcoxon符号秩检验采用混合效应有序逻辑回归模型。
20例RA患者共有25个置换关节和24个OJA。所有置换关节在基线时GSUS>1,92%的关节PDUS>1,而OJA和天然关节中GSUS>1(分别为37.5%、38%)和PDUS>1(分别为45.8%、62%)的证据较少。置换关节(P = 0.01,P = 0.007)和天然关节(两者P < 0.001)中,GSUS和PDUS半定量评分在治疗后有显著改善,但OJA没有。
在RA中,关节置换并不能消除或预防超声测量的滑膜炎,所有置换关节都有一些US滑膜炎的证据。US还可作为置换关节对治疗反应的潜在标志物。在超声RA临床试验中应考虑对置换关节的US滑膜炎进行评分。
ClinicalTrials.gov NCT01717859(2012年10月31日注册);ClinicalTrials.gov NCT02321930(2014年12月22日注册)。