Movahedi Mohammad, Weber Deborah, Akhavan Pooneh, Keystone Edward C
Ontario Best Practices Research Initiative, Toronto General Research Institute, University Health Network, Toronto, ON, Canada and Institute of Health Policy, Management, and Evaluation (IHPME), University of Toronto, Toronto, ON, Canada.
Institute of Health Policy, Management, and Evaluation (IHPME), University of Toronto, Toronto, ON, Canada.
ACR Open Rheumatol. 2020 Mar;2(3):188-194. doi: 10.1002/acr2.11123. Epub 2020 Mar 14.
Progressive rheumatoid arthritis (RA) is responsible for joint damage causing disabilities, but there is no agreement on which disease measures best predict radiographic progression. We aimed to determine which disease activity measures, including the disease activity score, the modified disease activity score in 28 joints with C-reactive protein testing (M-DAS28-CRP), the Clinical Disease Activity Index, and the Health Assessment Questionnaire Disability Index, at baseline and 3 months best predicted rapid radiographic progression (RRP) in patients with early RA.
Data were used from PREMIER, a 2-year, multicenter, double-blind, active comparator controlled study with methotrexate (MTX)-naïve patients with RA and active disease for less than 3 years. Treatments included adalimumab plus oral MTX, adalimumab, or oral MTX. Only patients in the MTX arm were analyzed in this study. RRP was defined as a change in the modified total Sharp score of less than 3.5 at month 12. The logistic regression analysis assessed the impact of measures at baseline and 3 months on RRP at 12 months. Best cutoff points of the M-DAS28-CRP were also estimated by using area under the receiver operating characteristic curve.
A total of 149 patients were included (female patients: n = 113 [75.8%]; positive rheumatoid factor: n = 127 [85.2%]; mean [SD] age: 52.9 [13.3] years; mean [SD] disease duration: 0.8 [0.9] year; mean [SD] M-DAS28-CRP: 6.3 [0.9]). After adjusting for potential confounders, only the M-DAS28-CRP at baseline (adjusted odds ratio [AOR] = 3.29; 95% confidence interval [CI]: 1.70-6.36) and 3 months (AOR = 2.56; 95% CI: 1.43-4.56) strongly predicted RRP at 12 months. M-DAS28-CRP of 4.5 and 2.6 at baseline and 3 months, respectively, maximized positive and negative predictive values for prediction of RRP.
The M-DAS28-CRP was a stronger predictor at baseline and 3 months for RRP compared with other disease activity measures. Removing tender joint count and patient global assessment from the DAS28-CRP improves prediction of RRP.
进行性类风湿关节炎(RA)会导致关节损伤并造成残疾,但对于哪种疾病指标能最佳预测影像学进展尚无定论。我们旨在确定哪些疾病活动指标,包括疾病活动评分、28个关节的改良疾病活动评分联合C反应蛋白检测(M-DAS28-CRP)、临床疾病活动指数以及健康评估问卷残疾指数,在基线期和3个月时能最佳预测早期RA患者的快速影像学进展(RRP)。
数据来自PREMIER研究,这是一项为期2年的多中心、双盲、活性对照药物对照研究,纳入了未使用过甲氨蝶呤(MTX)、患RA且疾病活动时间少于3年的患者。治疗方案包括阿达木单抗加口服MTX、阿达木单抗或口服MTX。本研究仅分析了MTX组的患者。RRP定义为第12个月时改良总Sharp评分变化小于3.5。逻辑回归分析评估了基线期和3个月时各指标对12个月时RRP的影响。还通过使用受试者工作特征曲线下面积估计了M-DAS28-CRP的最佳截断点。
共纳入149例患者(女性患者:n = 113 [75.8%];类风湿因子阳性:n = 127 [85.2%];平均[标准差]年龄:52.9 [13.3]岁;平均[标准差]病程:0.8 [0.9]年;平均[标准差]M-DAS28-CRP:6.3 [0.9])。在对潜在混杂因素进行校正后,仅基线期的M-DAS28-CRP(校正比值比[AOR] = 3.29;95%置信区间[CI]:1.70 - 6.36)和3个月时的M-DAS28-CRP(AOR = 2.56;95% CI:1.43 - 4.56)能强烈预测12个月时的RRP。基线期和3个月时M-DAS28-CRP分别为4.5和2.6时,预测RRP的阳性和阴性预测值最大化。
与其他疾病活动指标相比,M-DAS28-CRP在基线期和3个月时对RRP的预测能力更强。从DAS28-CRP中去除压痛关节计数和患者整体评估可提高对RRP的预测能力。