ReviewImaging study scores for ankylosing spondylitis
Introduction
The management of ankylosing spondylitis (AS) and other spondyloarthropathies is undergoing radical changes that are chiefly related to the introduction of TNFα antagonists. These agents have proved capable of improving the signs and symptoms of the disease, as well as overall short- and mid-term outcomes [1]. Studies of the potential structural effects of TNFα antagonists are ongoing in patients with rheumatoid arthritis. A prerequisite to the conduct of similar studies in AS is the availability of validated scoring systems for imaging studies that take into account the specific features of the disease, most notably at the sacroiliac joints and spine. Although work in this field is less advanced for AS than for rheumatoid arthritis, scores for AS are in the final phases of development and have a number of practical applications. Therefore, an overview of these scoring systems is timely.
The many available techniques for imaging the skeleton supply different levels of information. In practice, plain radiography and computed tomography (CT) provide structural information that represents the cumulative effect of the disease over time, indicating either stabilization or progression. These imaging methods are widely used for the diagnosis of AS, and the slow pace of radiological changes may explain the often unacceptably long diagnostic delays. In addition, plain radiography and CT show little sensitivity to short-term changes and are therefore of limited usefulness for evaluating treatment responses. In contrast, magnetic resonance imaging (MRI) with appropriate sequences [2] and power Doppler ultrasonography of the entheses provide an accurate assessment of inflammation at target sites and can show not only progression, but also reversal of abnormalities in the short-term.
A number of studies have led to the development of scoring systems for imaging studies in AS. These scoring systems are used in clinical research and therapeutic trials. Their contribution to everyday clinical practice and to the diagnosis of AS will need to be clarified.
Section snippets
Radiograph scores for AS
The sacroiliac joints and hips are the sites of interest on radiographs of the pelvis. In classification criteria for AS, a five-grade system (0–4) is used to describe sacroiliac joint involvement. Various patterns of inflammatory hip disease may be seen [3]. Hip involvement is associated with worse functional outcomes. Abnormalities of the sacroiliac joints and hips exhibit little sensitivity to change.
Plain radiographs of the spine may show the shiny corner sign (Romanus lesion), squaring of
MRI
Fewer data are available for MRI in AS. An OMERACT task force [17] has found that MRI is useful chiefly for assessing inflammatory changes, as opposed to structural changes. Published and unpublished scores for the sacroiliac joints and spine were compared using various MRI sequences and sections. Intra- and interobserver agreement and sensitivity to change were compared between the global and the analytical method. A validated standardized score suitable for use in everyday practice is being
Ultrasonography
B-mode ultrasonography coupled with power Doppler imaging (which visualizes vascular supply) shows entheseal lesions and detects evidence of inflammation. D'Agostino et al. [30] developed a five-grade ultrasound score for enthesitis, as follows: 1, vascularization at the cortical junction without abnormalities in B mode; 2a: vascularization associated with swelling and/or decreased echogenicity at the cortical junction in B mode; 3a: same as 2a plus erosions of cortical bone and/or
Conclusion
Imaging scores for AS will be used increasingly to meet the growing need for objective data on treatment effects. Although MRI scores hold promise for evaluating spinal inflammation and detecting changes over time, further validation and standardization are needed. With this respect, the conclusions of the OMERACT task force are impatiently awaited. For evaluating structural alterations, the mSASSS seems to be the best tool for clinical studies. However, the slow pace of lesion progression and,
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