ASDAS对强直性脊柱炎生物治疗患者药物生存率的可预测性:来自KOBIO注册中心的数据。

IF 3.4 2区 医学 Q2 RHEUMATOLOGY Therapeutic Advances in Musculoskeletal Disease Pub Date : 2023-10-09 eCollection Date: 2023-01-01 DOI:10.1177/1759720X231201714
Jinhyun Kim, Min Jung Kim, Geun Young Oh, Sun Kyung Lee, Taeeun Kim, Kichul Shin
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引用次数: 0

摘要

背景:强直性脊柱炎(AS)疾病活动性评分(ASDAS)主要用于评估AS患者的疾病活动性。目的:我们旨在研究ASDAS对巴斯AS疾病活动性指数(BASDAI)低的患者在生物治疗过程中药物生存的可预测性。设计:使用来自韩国风湿病生物制品和靶向治疗学院(KOBIO)注册中心的多中心、前瞻性、观察性前瞻性队列的数据。方法:研究人群包括2012年12月至2018年12月在KOBIO注册中心登记的患者。从数据库中收集基线人口统计数据和变量,如关节外表现、HLA-B27阳性、脊椎关节炎家族史、ASDAS C反应蛋白(CRP)、BASDAI和Bath as功能指数评分。在启动肿瘤坏死因子(TNF)抑制剂(TNFi)后,每年跟踪疾病活动指数。疾病活动被定义为高(ASDAS-CRP ⩾ 2.1,巴斯岱 ⩾ 4) 和低(ASDAS-CRP 结果:对1773例患者的数据进行了分析。在269名基线时BASDAI较低的患者中,151名(56.1%)患者的ASDAS-CRP较高,但在142名基线时ASDAS-CRP较低的病例中,只有24名(16.9%)患者的BASDAI较高。与高BASDAI患者相比,高ASDAS-CRP捕获了更多开始或改用TNFi的患者(分别为92.5%和84.8%,p 与82.5%相比 结论:ASDAS-CRP不仅在评估疾病活动性方面优于BASDAI,而且在1 一年可以作为TNFi治疗药物长期存活的标志。
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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The predictability of ASDAS on drug survival in patients with ankylosing spondylitis on biologic therapy: data from the KOBIO registry.

Background: The Ankylosing Spondylitis (AS) Disease Activity Score (ASDAS) is largely used for assessing disease activity in patients with AS.

Objectives: We aimed to investigate the predictability of ASDAS on drug survival in patients with low Bath AS Disease Activity Index (BASDAI) during biologic therapy.

Design: Using data from multi-center, prospective, observational prospective cohort, Korean College of Rheumatology Biologics and Targeted Therapy (KOBIO) registry.

Methods: The study population consisted of patients enrolled in the KOBIO registry from December 2012 to December 2018. The baseline demographic data and variables such as extra-articular manifestations, HLA-B27 positivity, family history of spondyloarthritis, ASDAS C-reactive protein (CRP), BASDAI, and Bath AS Functional Index scores were collected from the database. The disease activity indices were followed yearly after initiating a tumor necrosis factor (TNF) inhibitor (TNFi). Disease activities were defined as high (ASDAS-CRP ⩾ 2.1, BASDAI ⩾ 4) and low (ASDAS-CRP < 2.1, BASDAI < 4).

Results: Data from 1773 patients were analyzed. Among 269 patients with low BASDAI at baseline, 151 (56.1%) patients had high ASDAS-CRP, yet in 142 patients with low ASDAS-CRP at baseline, only 24 (16.9%) patients had a high BASDAI. High ASDAS-CRP captured more patients who had initiated or switched to a TNFi than those with high BASDAI (92.5% versus 84.8%, respectively, p < 0.001). Moreover, among AS patients with low BASDAI after 1 year of therapy, drug persistence in the following year was significantly lower in patients with high ASDAS than in those with low ASDAS (68.7% versus 82.5%, p < 0.001).

Conclusion: ASDAS-CRP not only has its advantages over BASDAI in assessing disease activity but also low ASDAS-CRP at 1 year can be a marker of long-term drug survival of TNFi therapy.

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来源期刊
CiteScore
6.80
自引率
4.80%
发文量
132
审稿时长
18 weeks
期刊介绍: Therapeutic Advances in Musculoskeletal Disease delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of musculoskeletal disease.
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