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Ultrasound and multi-biomarker disease activity score for assessing and predicting clinical response to tofacitinib treatment in patients with rheumatoid arthritis

机译:超声波和多生物标志物疾病活动评分用于评估和预测类风湿性关节炎患者对Tofacitinib治疗的临床反应

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Musculoskeletal ultrasound (MSUS) and the multi-biomarker disease activity (MBDA) score are outcome measures that may aid in the management of rheumatoid arthritis (RA) patients. This study evaluated tofacitinib response by MSUS/MBDA scores and assessed whether baseline MSUS/MBDA scores or their early changes predict later clinical response. Twenty-five RA patients treated with tofacitinib were assessed at baseline, 2, 6 and 12-weeks. Power doppler (PDUS) and gray scale (GSUS) ultrasound scores, MBDA score, clinical disease activity index (CDAI), and disease activity score (DAS28) were obtained. Pearson correlations and multiple linear regression models were used to evaluate associations and identify predictors of response to therapy. MSUS, MBDA scores, CDAI, and DAS28 improved significantly over 12?weeks (p??0.0001). Baseline MSUS and MBDA score correlated with each other, and with 12-week changes in CDAI/DAS28 (r?=?0.45–0.62, p??0.05), except for GSUS with DAS28. Two-week change in MSUS correlated significantly with 12-week changes in CDAI/DAS28 (r?=?0.42–0.57, p??0.05), except for early change in PDUS with 12-week change in CDAI. Regression analysis demonstrated significant independent associations between baseline PDUS/MBDA score and 6-week change in CDAI/DAS28, with adjustment for baseline CDAI/DAS28 (all p??0.05); and between baseline MBDA scores and 12-week change in DAS28 (p?=?0.03). RA patients treated with tofacitinib for 12?weeks demonstrated improvement by clinical, imaging, and biomarker end-points. Baseline PDUS and MBDA score were predictive of CDAI and DAS28 responses. This is the first study to evaluate early measurements of MSUS and MBDA score as predictors of clinical response in RA patients treated with tofacitinib. ClinicalTrials.gov NCT02321930 (registered 12/22/2014).
机译:肌肉骨骼超声(MSU)和多生物标志物疾病活动(MBDA)评分是可能有助于管理类风湿性关节炎(RA)患者的结果措施。本研究评估了MSUS / MBDA评分的TOFACITINIB响应,并评估了基线MSUS / MBDA评分或其早期变化预测临床反应。在基线,2,6和12周的基线中评估了用Tofacitinib治疗的二十五名RA患者。获得功率多普勒(PDU)和灰度(GSUS)超声评分,MBDA评分,临床疾病活动指数(CDAI)和疾病活动评分(DAS28)。 Pearson相关性和多元线性回归模型用于评估关联并识别响应治疗的预测因子。 MSU,MBDA分数,CDAI和DAS28显着提高了12个?周(P?&?0.0001)。基线MSU和MBDA分数相互关联,CDAI / DAS28的12周变化(R?= 0.45-0.62,p≤≤0.05),除了使用DAS28的GSU。在CDAI / DAS28的12周变化中,MSU的两周变化显着相关(R?= 0.42-0.57,p≤0.05),除了PDU的早期变化,CDAI的12周变化。回归分析显示基线PDU / MBDA评分与CDAI / DAS28的6周变化之间的重要独立关联,调整基线CDAI / DAS28(所有P?0. 0.05);在基线MBDA分数和12周的DAS28变化之间(P?= 0.03)。 Ra患者用噻acacitinib治疗12?几周通过临床,成像和生物标志物终点进行了改善。基线PDU和MBDA得分是预测CDAI和DAS28的反应。这是第一次评估MSU和MBDA评分的早期测量作为Rafacitinib治疗的RA患者临床反应预测因素的研究。 ClinicalTrials.gov NCT02321930(注册12/22/2014)。

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