Predominant ligament-centric soft-tissue involvement differentiates axial psoriatic arthritis from ankylosing spondylitis

IF 29.4 1区 医学 Q1 RHEUMATOLOGY Nature Reviews Rheumatology Pub Date : 2023-11-02 DOI:10.1038/s41584-023-01038-9
Dennis McGonagle, Paula David, Tom Macleod, Abdulla Watad
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Abstract

Since the original description of spondyloarthritis 50 years ago, results have demonstrated similarities and differences between ankylosing spondylitis (AS) and axial psoriatic arthritis (PsA). HLA-B27 gene carriage in axial inflammation is linked to peri-fibrocartilaginous sacroiliac joint osteitis, as well as to spinal peri-entheseal osteitis, which is often extensive and which provides a crucial anatomical and immunological differentiation between the AS and PsA phenotypes. Specifically, HLA-B27-related diffuse bone marrow oedema (histologically an osteitis) and bone marrow fatty corners detected via magnetic resonance imaging, as well as radiographic changes such as sacroiliitis, vertebral squaring, corner erosions and Romanus lesions, all indicate initial bone phenotypes in HLA-B27+ axial disease. However, in much of PsA with axial involvement, enthesitis primarily manifests in ligamentous soft tissue as ‘ligamentitis’, with characteristic lesions that include para-syndesmophytes and sacroiliac joint bony sparing. Like axial PsA, diffuse idiopathic skeletal hyperostosis phenotypes, which can be indistinguishable from PsA, exhibit a thoracic and cervical spinal ligamentous soft-tissue tropism, clinically manifesting as syndesmophytosis that is soft-tissue-centric, including paravertebral soft-tissue ossification and sacroiliac soft-ligamentous ossification instead of joint-cavity fusion. The enthesis bone and soft tissues have radically different immune cell and stromal compositions, which probably underpins differential responses to immunomodulatory therapy, especially IL-23 inhibition. In this Perspective, the authors propose that despite the known similarities between ankylosing spondylitis and axial psoriatic arthritis, the localization of inflammation to bone in ankylosing spondylitis and to ligamentous soft tissue in axial axial psoriatic arthritis differentiates these diseases and has important implications for diagnosis, pathology and treatment.

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主要以韧带为中心的软组织受累将轴性银屑病关节炎与强直性脊柱炎区分开来。
自从50年前对脊椎关节炎的最初描述以来,研究结果证明了强直性脊柱炎(AS)和轴性银屑病关节炎(PsA)之间的相似性和差异性。轴性炎症中的HLA-B27基因携带与纤维软骨周围骶髂关节炎以及脊髓端部周围骨炎有关,后者通常是广泛的,在as和PsA表型之间提供了至关重要的解剖学和免疫学分化。具体而言,通过磁共振成像检测到的HLA-B27相关的弥漫性骨髓水肿(组织学上是一种骨炎)和骨髓脂肪角,以及骶髂关节炎、椎体方正、角侵蚀和Romanus病变等放射学变化,都表明HLA-B27+轴性疾病的初始骨表型。然而,在大多数轴位受累的PsA中,附着点炎主要表现为韧带软组织“韧带炎”,其特征性病变包括韧带旁植物和骶髂关节骨保留。与轴性PsA一样,与PsA无法区分的弥漫性特发性骨骼增生表型表现出胸椎和颈椎韧带软组织向性,临床表现为以软组织为中心的韧带骨化,包括椎旁软组织骨化和骶髂软韧带骨化,而不是关节腔融合。骨端和软组织具有完全不同的免疫细胞和基质成分,这可能是对免疫调节治疗,特别是IL-23抑制的不同反应的基础。
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来源期刊
Nature Reviews Rheumatology
Nature Reviews Rheumatology 医学-风湿病学
CiteScore
29.90
自引率
0.90%
发文量
137
审稿时长
6-12 weeks
期刊介绍: Nature Reviews Rheumatology is part of the Nature Reviews portfolio of journals. The journal scope covers the entire spectrum of rheumatology research. We ensure that our articles are accessible to the widest possible audience.
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