Department of Medicine, Division of Rheumatology, University of Alberta, 568 Heritage Medical Research Building, T6G 2S2, Edmonton, Canada.
CARE Arthritis, Edmonton, Canada.
Arthritis Res Ther. 2023 Apr 28;25(1):70. doi: 10.1186/s13075-023-03055-1.
To (i) determine whether sustained disease activity states, as measured by Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Ankylosing Spondylitis Disease Activity Score (ASDAS), impact function, and (ii) evaluate characteristics predicting sustained low functional impairment in a prospective axial spondyloarthritis (axSpA) cohort.
Biologic Treatment Registry Across Canada (BioTRAC) was a multi-center, prospective registry that collected real-world data on axSpA patients receiving infliximab or golimumab between 2006 and 2017. Generalized estimating equations (GEE) were used to test baseline characteristics, treatment, and duration (at 6 and 12 months vs. only at 6 or 12 months vs. neither) of low BASDAI (< 3), ASDAS-inactive disease (ID)(< 1.3), and ASDAS-low disease activity (LDA) in predicting sustained low Bath Ankylosing Spondylitis Functional Index (BASFI)(< 3) between 12 and 18 months. The adjusted impact of achieving low disease state at 6 and/or 12 months on BASFI at 18 months was analyzed by generalized linear models.
Eight hundred ten patients were enrolled. 33.7%, 13.4%, and 24.7% achieved sustained low BASDAI, ASDAS-ID, and ASDAS-LDA, respectively. In univariable GEE of baseline variables, age and baseline BASDAI, BASFI, and ASDAS significantly predicted sustained low BASFI. In multivariable GEE, sustained low BASDAI (p < 0.001), low BASDAI only at 6 or 12 months (p = 0.001), and baseline BASFI (p < 0.001) were the only predictors of sustained low BASFI. Sustained ASDAS-ID (p = 0.040) and ASDAS-LDA (p < 0.001) were also predictors when forced into the model. Similar results were obtained when evaluating the BASFI score at 18 months.
Sustained BASDAI < 3 may be a valid and feasible target for a treat-to-target strategy in axSpA having function as treatment goal.
(i)确定通过巴斯强直性脊柱炎疾病活动指数(BASDAI)和强直性脊柱炎疾病活动评分(ASDAS)测量的持续疾病活动状态是否会影响功能,以及(ii)评估前瞻性轴性脊柱关节炎(axSpA)队列中持续低功能障碍的预测特征。
加拿大生物治疗登记处(BioTRAC)是一个多中心、前瞻性登记处,收集了 2006 年至 2017 年接受英夫利昔单抗或戈利木单抗治疗的 axSpA 患者的真实世界数据。使用广义估计方程(GEE)测试基线特征、治疗和持续时间(6 个月和 12 个月时与仅在 6 个月或 12 个月时与均未达到)低 BASDAI(<3)、ASDAS 无疾病活动(ID)(<1.3)和 ASDAS 低疾病活动(LDA)在预测 12 至 18 个月时持续低巴斯强直性脊柱炎功能指数(BASFI)(<3)方面的预测作用。通过广义线性模型分析 6 个月和/或 12 个月时达到低疾病状态对 18 个月时 BASFI 的影响。
共纳入 810 例患者。分别有 33.7%、13.4%和 24.7%的患者持续低 BASDAI、ASDAS-ID 和 ASDAS-LDA。在单变量 GEE 的基线变量中,年龄和基线 BASDAI、BASFI 和 ASDAS 显著预测持续低 BASFI。在多变量 GEE 中,持续低 BASDAI(p<0.001)、仅在 6 个月或 12 个月时低 BASDAI(p=0.001)和基线 BASFI(p<0.001)是持续低 BASFI 的唯一预测因素。持续的 ASDAS-ID(p=0.040)和 ASDAS-LDA(p<0.001)在模型中也是预测因素。当评估 18 个月时的 BASFI 评分时,也得到了类似的结果。
持续的 BASDAI<3 可能是 axSpA 中以功能为治疗目标的靶向治疗策略的一个有效和可行的目标。