首页> 外文期刊>International journal of rheumatology >The Nonradiographic Axial Spondyloarthritis, the Radiographic Axial Spondyloarthritis, and Ankylosing Spondylitis: The Tangled Skein of Rheumatology
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The Nonradiographic Axial Spondyloarthritis, the Radiographic Axial Spondyloarthritis, and Ankylosing Spondylitis: The Tangled Skein of Rheumatology

机译:非显影性轴向脊椎炎,射线照相轴向脊椎炎和强直性脊柱炎:风湿病的缠结

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摘要

Since 1984 the diagnosis of ankylosing spondylitis (AS) has been based upon the modified New York (mNY) criteria with mandatory presence of radiographic sacroiliitis, without which the diagnosis is not tenable. However, it may take years or decades for radiographic sacroiliitis to develop delaying the diagnosis for long periods. It did not matter in the past because no effective treatment was available. However, with the availability of a highly effective treatment, namely, tumour necrosis factor-α inhibitors (TNFi), the issue of early diagnosis of AS acquired an urgency. The Assessment of SpondyloArthritis International Society (ASAS) classification criteria published in 2009 was a significant step towards this goal. These criteria described an early stage of the disease where sacroiliitis was demonstrable only on MRI but not on standard radiograph. Therefore, this stage of the disease was labelled “nonradiographic axial SpA” (nr-axSpA). But questions have been raised if, in search of early diagnosis, specificity was compromised. The Federal Drug Administration (FDA, USA) withheld approval for the use of TNFi in patients with nr-axSpA because of issues related to the specificity of these criteria. This review attempts to clarify some of these aspects of the nr-axSpA-AS relationship and also tries to answer the question whether ASAS classifiable radiographic axial spondyloarthritis (r-axSpA) term can be interchangeably used with the term AS.
机译:自1984年以来,诊断强直性脊柱炎(AS)基于修改的纽约(MNY)标准,其强制性存在放射学骶髂炎,无论诊断都不是危险的。然而,射线照相骶髂炎可能需要数年或数十年来发展长期延迟诊断。它过去无关紧要,因为没有有效的治疗。然而,随着高效治疗的可用性,即肿瘤坏死因子-α抑制剂(TNFI),早期诊断的问题是获得的紧急性。 2009年发布的脊椎关节炎国际社会(ASAS)分类标准的评估是实现这一目标的重要一步。这些标准描述了疾病的早期阶段,其中骶髂炎仅在MRI上证明,但不是标准射线照片。因此,该疾病的这种阶段被标记为“非显影轴向SPA”(NR-AXSPA)。但是,如果寻找早期诊断,具体妥协,则提出了问题。由于与这些标准的特异性有关的问题,联邦药物管理局(FDA,USA)批准用于使用NR-AXSPA患者的TNFI。该审查试图阐明NR-AXSPA的一些方面 - 作为关系,并试图回答ASAS可分类的放射线轴向脊髓灰质炎(R-AXSPA)术语的问题可以与术语互换使用。

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