Abstract

We would like to comment on magnetic resonance imaging (MRI) assessment of bone marrow lesions (BMLs) in osteoarthritis (OA) research from a radiologic perspective. Selection of pulse sequences that are able to depict the maximum extent of BMLs is of paramount importance for subsequent correct assessment of the size of these lesions. A recently published article investigating a canine OA model by MRI suggested that to accurately assess semiquantitative size and extent of BMLs a combination of different pulse sequences should be used, and that this information could also apply to human clinical studies 1 . In that study the authors used a protocol of T1-weighted threedimensional (3D) fast gradient recalled echo (GRE), sagittal fat-suppressed (FS) 3D spoiled gradient echo at a steady state (SPGR), and sagittal T2-weighted fast spin echo (FSE) with fat saturation sequences and assessed BMLs using a semiquantitative scoring approach. Another article by the same research group published in ‘‘Annals of the Rheumatic Diseases’’ recently investigated subchondral bone lesions with a quantitative MRI approach 2 . Acquisition of BMLs in that publication was performed on a 1.5 T system using a single 3D fast imaging with steady state precession (FISP) e sequence, a GRE-type sequence. While it has been shown that GRE-type sequences such as SPGR, fast low angle shot (FLASH), 3-point Dixon, double echo steady state (DESS) and others are very sensitive in delineating subchondral cysts, ‘‘even with robust FS or WE [water excitation], these sequences are notoriously

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