Construct validity and responsiveness of ASAS Health Index assessed in two longitudinal studies of tumour necrosis factor alpha inhibitor initiation and dose reduction in patients with axial spondyloarthritis.

IF 5.1 2区 医学 Q1 RHEUMATOLOGY
Mate Lorincz, Mikkel Østergaard, Marie Wetterslev, Inge Juul Sørensen, Ole Rintek Madsen, Sara Nysom Christiansen, Merete Lund Hetland, Mads Bakkegaard, Mette Klarlund, Anne Duer, Mikael Boesen, Kasper Kjærulf Gosvig, Susanne Juhl Pedersen
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引用次数: 0

Abstract

Background: The Assessment of SpondyloArthritis international Society Health Index (ASAS HI) is a novel questionnaire of global functioning for patients with axial spondyloarthritis (SpA).

Objective: The objective was to assess the construct validity, discriminatory ability and responsiveness of ASAS HI in relation to patient-reported outcome measures (PROMs), MRI and radiography.

Methods: Data from two longitudinal studies with tumour necrosis factor inhibitor (TNFi) initiation (novel MRI And biomarkers in Golimumab-treated patients with axial spondyloarthritis (MANGO): n=45) respectively tapering (Dose adjustment of Biological treatment in patients with SpA (DOBIS): n=106) were used. Analyses included a wide panel of PROMs, MRI and radiography scores of the spine and sacroiliac joints (SIJs).

Results: In the MANGO study, 30 (68%) patients were clinical responders at week 16. In the DOBIS study, 105 (99%) patients flared after mean (SD; min-max) 31 (17; 2.7-81) weeks. After initiation of TNF inhibitor in MANGO, ASAS HI significantly decreased from baseline to week 4, 16 and 52. In DOBIS, ASAS significantly increased from baseline to the flare visit and significantly decreased from the flare visit to week 96. In multivariate regression models, ASAS HI was independently associated with Spondyloarthritis Research Consortium of Canada MRI SIJ Inflammation score, Canada-Denmark MRI Spine Inflammation score, EuroQol, Ankylosing Spondylitis Disease Activity Index, Bath Ankylosing Spondylitis Disease Activity Index and Patient Global. Patients stratified according to ASAS HI health status groups (good, moderate, poor) at baseline and change categories (absolute and percentage change) from baseline to week 16/flare showed good discriminatory ability for almost all outcome variables (p≤0.001). ASAS HI had a large responsiveness in MANGO (standardised response mean (SRM)=-1.3, effect size (ES)=-1.7) and moderate responsiveness in DOBIS (SRM=0.7, ES=0.6).

Conclusion: ASAS HI showed good construct validity, discriminatory ability and responsiveness.

Trial registration number: ClinicalTrials.gov: NCT02011386.

在两项纵向研究中评估了肿瘤坏死因子α抑制剂的启动和剂量减少对轴性脊柱炎患者的ASAS健康指数的构建有效性和反应性。
背景:国际社会健康指数评估(ASAS HI)是一项针对轴性脊柱炎(SpA)患者的整体功能的新型问卷。目的:目的是评估ASAS HI与患者报告的结果测量(PROMs)、MRI和x线摄影的结构效度、区分能力和反应性。方法:采用两项纵向研究的数据,分别采用肿瘤坏死因子抑制剂(TNFi)起始(golimumab治疗的轴性脊柱炎患者的新型MRI和生物标志物(MANGO): n=45)逐渐减少(SpA患者的生物治疗剂量调整(DOBIS): n=106)。分析包括广泛的PROMs, MRI和脊柱和骶髂关节(sij)的x线摄影评分。结果:在MANGO研究中,30例(68%)患者在第16周达到临床应答。在DOBIS研究中,105例(99%)患者在平均(SD;Min-max) 31 (17;-81年2.7)周。在MANGO开始TNF抑制剂治疗后,ASAS HI从基线到第4,16和52周显著下降。在DOBIS中,ASAS从基线到耀斑发作显著增加,从耀斑发作到第96周显著降低。在多元回归模型中,ASAS HI与加拿大脊柱炎研究联盟MRI SIJ炎症评分、加拿大-丹麦MRI脊柱炎症评分、EuroQol、强直性脊柱炎疾病活动指数、Bath强直性脊柱炎疾病活动指数和Patient Global独立相关。根据基线时ASAS HI健康状况组(好、中、差)和从基线到第16周/发作的变化类别(绝对和百分比变化)对患者进行分层,几乎所有结果变量都显示出良好的区分能力(p≤0.001)。ASAS HI在MANGO中有较大的反应性(标准化反应均值(SRM)=-1.3,效应量(ES)=-1.7),在DOBIS中有中等的反应性(SRM=0.7, ES=0.6)。结论:ASAS HI具有良好的构念效度、区分能力和反应性。试验注册号:ClinicalTrials.gov: NCT02011386。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
RMD Open
RMD Open RHEUMATOLOGY-
CiteScore
7.30
自引率
6.50%
发文量
205
审稿时长
14 weeks
期刊介绍: RMD Open publishes high quality peer-reviewed original research covering the full spectrum of musculoskeletal disorders, rheumatism and connective tissue diseases, including osteoporosis, spine and rehabilitation. Clinical and epidemiological research, basic and translational medicine, interesting clinical cases, and smaller studies that add to the literature are all considered.
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