Verhoeven Maxime M A, Tekstra Janneke, Marijnissen Anne C A, Meier Anna J L, Westgeest Antonius A A, Lafeber Floris P J G, Jacobs Johannes W G, van Laar Jacob M, Welsing Paco M J
Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht.
Department of Rheumatology, Máxima MC, Eindhoven, The Netherlands.
Rheumatol Adv Pract. 2021 Jan 28;5(1):rkab004. doi: 10.1093/rap/rkab004. eCollection 2021.
The aims were to determine the ability of the HandScan [assessing inflammation in hand and wrist joints using optical spectral transmission (OST)] to measure RA disease activity longitudinally, compared with DAS28, and to determine whether short-term (i.e. 1 month) changes in the OST score can predict treatment response at 3 or 6 months.
Participants visited the outpatient clinic before the start of (additional) RA medication and 1, 3 and 6 months thereafter. Disease activity was monitored at each visit with the HandScan and DAS28 in parallel. A mixed effects model with DAS28 as the outcome variable with a random intercept at patient level, visit month and DAS28 one visit earlier was used to evaluate whether changes in the OST score are related to changes in DAS28. Binary logistic regression was used to test the predictive value of short-term changes in the OST score together with the baseline OST score for achievement of treatment response (EULAR or ACR criteria). All models were adjusted for RA stage (early or established).
In total, 64 RA patients were included. One unit change in OST score was found to be related to an average DAS28 change of 0.03 (95% CI: 0.01, 0.06, = 0.03). When adding OST score as a variable in the longitudinal model, the ability of the model to estimate DAS28 (i.e. explained variance) increased by 2%, to 59%. Neither baseline OST score nor short-term change in OST score was predictive for treatment response at 3 or 6 months.
A longitudinal association of OST score with DAS28 exists, although explained variance is low. The predictive ability of short-term changes in HandScan for treatment response is limited.
本研究旨在确定HandScan(利用光谱透射法评估手和腕关节炎症)纵向测量类风湿关节炎(RA)疾病活动度的能力,并与DAS28进行比较,同时确定OST评分的短期(即1个月)变化是否能预测3个月或6个月时的治疗反应。
参与者在开始(额外)RA药物治疗前及之后的1、3和6个月到门诊就诊。每次就诊时同时使用HandScan和DAS28监测疾病活动度。以DAS28为结果变量,在患者水平、就诊月份和前一次就诊的DAS28处设置随机截距,采用混合效应模型评估OST评分变化是否与DAS28变化相关。采用二元逻辑回归检验OST评分的短期变化与基线OST评分对治疗反应(依欧洲抗风湿病联盟或美国风湿病学会标准)达成情况的预测价值。所有模型均根据RA分期(早期或已确诊)进行调整。
共纳入64例RA患者。发现OST评分每变化1个单位与DAS28平均变化0.03相关(95%置信区间:0.01,0.06,P = 0.03)。在纵向模型中加入OST评分作为变量后,模型估计DAS28的能力(即解释方差)提高了2%,达到59%。基线OST评分和OST评分的短期变化均不能预测3个月或6个月时的治疗反应。
OST评分与DAS28存在纵向关联,尽管解释方差较低。HandScan短期变化对治疗反应的预测能力有限。