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在ABILITY-1临床试验中,非放射性中轴型脊柱关节炎患者的ASAS40和ASDAS临床反应转化为身体功能、健康相关生活质量和工作效率的显著改善。

ASAS40 and ASDAS clinical responses in the ABILITY-1 clinical trial translate to meaningful improvements in physical function, health-related quality of life and work productivity in patients with non-radiographic axial spondyloarthritis.

作者信息

van der Heijde Désirée, Joshi Avani, Pangan Aileen L, Chen Naijun, Betts Keith, Mittal Manish, Bao Yanjun

机构信息

Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands,

Health Economics & Outcomes Research.

出版信息

Rheumatology (Oxford). 2016 Jan;55(1):80-8. doi: 10.1093/rheumatology/kev267. Epub 2015 Aug 27.

Abstract

OBJECTIVE

To assess the impact of achieving Assessment in SpondyloArthritis international Society 40% (ASAS40) response or an Ankylosing Spondylitis Disease Activity Score inactive disease (ASDAS-ID) state on patient-reported outcomes (PROs) among patients with non-radiographic axial SpA (nr-axSpA).

METHODS

Data are from ABILITY-1, a phase 3 trial of adalimumab vs placebo in nr-axSpA patients. PROs included the HAQ for Spondyloarthropathies (HAQ-S), 36-item Short Form Health Survey (SF-36) physical component summary (PCS) score and Work Productivity and Activity Impairment Questionnaire. Patients were grouped by clinical response using ASAS40 response and ASDAS disease states at week 12. Changes in PROs from baseline to week 12 were compared between groups using analysis of covariance with adjustment for baseline scores.

RESULTS

At week 12, 47 of 179 patients were ASAS40 responders and 26 of 176 patients achieved ASDAS-ID (ASDAS <1.3). Compared with non-responders (n = 132), ASAS40 responders (n = 47) had a significantly greater improvement in mean HAQ-S (-0.65 vs -0.05, P < 0.0001), SF-36 PCS (12.4 vs 0.7, P < 0.0001), presenteeism (-24.7 vs -2.2, P < 0.0001), overall work impairment (-23.9 vs -2.5, P < 0.0001) and activity impairment (-33.5 vs -0.9, P < 0.0001) at week 12. Similarly, ASDAS-ID, ASDAS clinically important improvement (ASDAS-CII; improvement >1.1) and major improvement (ASDAS-MI; improvement >2.0) were associated with significantly greater improvements from baseline in the majority of the PROs.

CONCLUSION

Among nr-axSpA patients, ASAS40, ASDAS-CII and ASDAS-MI response and achievement of ASDAS-ID were associated with statistically significant and clinically meaningful improvements in physical function, health-related quality of life and work productivity in a higher percentage of patients.

摘要

目的

评估达到脊柱关节炎国际协会40%反应(ASAS40)或强直性脊柱炎疾病活动评分无疾病活动(ASDAS-ID)状态对非放射学轴向脊柱关节炎(nr-axSpA)患者报告结局(PROs)的影响。

方法

数据来自ABILITY-1,这是一项在nr-axSpA患者中比较阿达木单抗与安慰剂的3期试验。PROs包括脊柱关节病健康评估问卷(HAQ-S)、36项简短健康调查(SF-36)身体成分总结(PCS)评分以及工作生产力和活动障碍问卷。在第12周时,根据ASAS40反应和ASDAS疾病状态将患者按临床反应分组。使用协方差分析并对基线评分进行调整,比较各组从基线到第12周PROs的变化。

结果

在第12周时,179例患者中有47例为ASAS40反应者,176例患者中有26例达到ASDAS-ID(ASDAS<1.3)。与无反应者(n = 132)相比,ASAS40反应者(n = 47)在第12周时平均HAQ-S(-0.65对-0.05,P<0.0001)、SF-36 PCS(12.4对0.7,P<0.00

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5179/4676905/588dad27939b/kev267f1p.jpg

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