Structural disease modification in axial spondyloarthritis

被引:2
|
作者
Dinneen, Brona [1 ,4 ]
Shea, Finbar O. ' [1 ,2 ]
Gensler, Lianne [3 ]
机构
[1] St James Hosp, Dept Rheumatol, Dublin, Ireland
[2] Trinity Coll Dublin, Sch Med, Dublin, Ireland
[3] Univ Calif San Francisco, UCSF Diabet Ctr, Dept Med, San Francisco, CA 94143 USA
[4] St James Hosp, Rheumatol Dept, James St, Dublin, Ireland
来源
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY | 2023年 / 37卷 / 03期
关键词
Axial spondylarthritis; Ankylosing spondylitis; Spondylarthritis; Radiographic progression; Imaging; Risk factors; Smoking; Structural progression; Non-Steroidal anti-in flammatory agents; Antirheumatic agents; Disease progression; Outcomes assessment; Tumor necrosis factor-alpha; Diagnostic imaging; SPINAL RADIOGRAPHIC PROGRESSION; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; ANKYLOSING-SPONDYLITIS; DOUBLE-BLIND; INFLAMMATORY PATHWAYS; PSORIATIC-ARTHRITIS; EFFICACY; SAFETY; MULTICENTER; ADALIMUMAB;
D O I
10.1016/j.berh.2023.101898
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
"Disease modification" in axial spondyloarthritis (axSpA) seeks to not only alleviate clinical symptoms but also alter the disease's natural course by impeding new bone formation. Recent years have witnessed the effectiveness of treatments, including biologics and nonsteroidal anti-inflammatory drugs, in managing axSpA symptoms. Emerging evidence points toward their potential impact on slowing structural disease progression. This comprehensive review centers on the pivotal role of inhibiting new bone formation in axSpA disease modification. It delves into the significance of imaging techniques for assessing disease progression and explores the disease-modifying properties of available axSpA treatments, encompassing NSAIDs, TNF inhibitors, IL-17 inhibitors, and JAK inhibitors. This article offers valuable insights into the evolving landscape of disease modification strategies in axial spondyloarthritis, highlighting the multifaceted approaches used to attain these objectives.(c) 2023 Elsevier Ltd. All rights reserved.
引用
收藏
页数:12
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