New bone formation at the sacroiliac joint in axial spondyloarthritis: characterization of backfill in MRI and CT

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Abstract

Objective: MRI findings of the SI joint space in axial SpA (axSpA) include inflammation and fat metaplasia inside an erosion; the latter is also termed ‘backfill’. We compared such lesions with CT to better characterize whether they represent new bone formation. Methods: We identified patients with axSpA who underwent both CT and MRI of the SI joints in two prospective studies. MRI datasets were jointly screened by three readers for joint space–related findings and grouped into three categories: type A—high short tau inversion recovery (STIR) and low T1 signal; type B—high signal in both sequences; type C—low STIR and high T1 signal. Image fusion was used to identify MRI lesions in CT before we measured Hounsfield units (HU) in each lesion and surrounding cartilage and bone. Results: Ninety-seven patients with axSpA were identified and we included 48 type A, 88 type B, and 84 type C lesions (maximum 1 lesion per type and joint). The HU values were 73.6 (S.D. 15.0) for cartilage, 188.0 (S.D. 69.9) for spongious bone, 1086.0 (S.D. 100.3) for cortical bone, 341.2 (S.D. 96.7) for type A, 359.3 (S.D. 153.5) for type B and 446.8 (S.D. 123.0) for type C lesions. Lesion HU values were significantly higher than those for cartilage and spongious bone, but lower than those for cortical bone (P < 0.001). Type A and B lesions showed similar HU values (P ¼ 0.93), whereas type C lesions were denser (P < 0.001). Conclusion: All joint space lesions show increased density and might contain calcified matrix, suggesting new bone formation, with a gradual increase in the proportion of calcified matrix towards type C lesions (backfill).

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Diekhoff, T., Poddubnyy, D., Proft, F., Ziegeler, K., Deppe, D., Niedermeier, C., & Hermann, K. G. A. (2023). New bone formation at the sacroiliac joint in axial spondyloarthritis: characterization of backfill in MRI and CT. Rheumatology (United Kingdom), 62(12), 3893–3898. https://doi.org/10.1093/rheumatology/kead142

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