We would like to comment on magnetic resonance imaging (MRI) assessment of focal cartilage defects in osteoarthritis (OA) research from a radiologic point of view. Doré et al recently reported the association between baseline tibial bone area and tibial subchondral bone mineral density (BMD) with tibial cartilage defect development and cartilage volume loss (1). They concluded that bone area predicted medial and lateral cartilage defect development and medial cartilage volume loss, while subchondral BMD predicted medial defect development, but not cartilage loss. Tibial cartilage defects were graded on a scale of 0-4 using T1-weighted fat suppressed 3-dimensional (3-D) gradient-recalled acquisition in the steady-state sequence, which is one of several gradientrecalled echo (GRE) type of sequences. GRE-type sequences such as 3-D spoiled gradient-recalled acquisition in the steadystate (SPGR), fast low-angle shot, 3-point Dixon, and doubleecho steady-state are well suited for depicting the cartilage volume, and thus they are the sequence of choice for quantitative (volumetric) analysis of cartilage (2,3).However, for depicting subtle cartilage abnormalities, GRE-type sequences are less suited than fluid-sensitive sequences (such as fat-suppressed intermediate [IM]-weighted, proton density [PD]-weighted, or fast spin-echo [FSE] T2-weighted image sequences [4,5]). With fat-suppressed IM-, PD-, and T2-weighted FSE sequences, normal hyaline cartilage has intermediate signal intensity, and intraarticular fluid is bright and displays good contrast due to an "arthrographic" effect that identifies surface abnormalities as well as abnormalities in cartilage matrix (6) ( Figures 1A and B). Moreover, GRE-type sequences are very susceptible to artifacts (motion artifacts from long imaging time and susceptibility artifacts), leading to difficulty differentiating between true cartilage defect and signal changes due to artifact (Figures 1C and D).Recent studies applying MRI semiquantitative assessment of focal cartilage defects use fluid-sensitive sequences (7-9) rather than GRE-type sequences because of these difficulties. Doré and colleagues' choice of MR sequence for assessment of focal cartilage defects is therefore not appropriate, according to the latest reports that advocate using these techniques. The authors should have at least acknowledged these facts in their report.As a consequence of the inadequate choice of pulse sequences in their study, it is unclear what the results presented by this group pertaining to cartilage defects represent. Detection of lesions and the estimations of their size will be inaccurate, so adequately interpreting the results and drawing conclusions based upon them seems impossible. We would strongly encourage others to use appropriate MRI pulse sequences to evaluate focal cartilage abnormalities, and if there is uncertainty, to seek advice from adequately trained musculoskeletal radiologists when developing studies, in order to achieve highest possible image quality with currently available t...