Glaser C, Mendlik T, Dinges J, Weber J, Stahl R, Trumm C, Reiser M
Institut für Klinische Radiologie, Klinikum der LMU München/Grosshadern, München, Germany.
Magn Reson Med. 2006 Sep;56(3):527-34. doi: 10.1002/mrm.21005.
Seven T2 maps (multiecho (ME) sequence: 3000 ms, eight echoes with 13.2 ms of echo spacing, 20 sections) and T1-weighted (T1-w) fast low-angle shot (FLASH-water excitation (WE)) data sets from four imaging sessions (right patellae of 10 healthy volunteers) were obtained. A segmentation of cartilage (WE sequence) was overlaid on the ME data and T2 values were calculated for total cartilage, three layers, three facets (global), and 240 ROIs (regional). Reproducibility (precision error) was calculated as the root mean square average (RMSA) of the individual coefficients of variation (COVs, %) and standard deviations (SDs, ms) for intra- and intersession reproducibility. The precision error was 3-7% and 6-29% for global and regional T2, respectively. There was no difference between intra- and intersession reproducibility, but there was worse reproducibility in the superficial layers compared to the deeper layers. Peripheral ROI reproducibility (mean=13%) was worse than in the central portions (mean=11%), but omission of the periphery did not positively affect the globally calculated T2 reproducibility. The precision errors were small compared to reported changes in diseased cartilage, suggesting good discriminatory power of the technique. Our data provide a first estimate of global and regional reproducibility errors of T2 in healthy cartilage, and may serve as a basis for sample size calculations and aid study designs for longitudinal and cross-sectional trials in osteoarthritis (OA).
获取了来自四个成像时段(10名健康志愿者的右髌骨)的七幅T2图(多回波(ME)序列:3000毫秒,八个回波,回波间隔为13.2毫秒,20层)以及T1加权(T1-w)快速低角度激发(FLASH-水激发(WE))数据集。对软骨进行分割(WE序列)并叠加在ME数据上,计算全层软骨、三层、三个面(整体)以及240个感兴趣区(局部)的T2值。再现性(精确误差)计算为个体变异系数(COV,%)和标准差(SD,毫秒)在时段内和时段间再现性的均方根平均值(RMSA)。整体和局部T2的精确误差分别为3%-7%和6%-29%。时段内和时段间再现性无差异,但表层的再现性比深层差。周边感兴趣区的再现性(平均值=13%)比中央部分(平均值=11%)差,但忽略周边对整体计算的T2再现性没有积极影响。与报道的病变软骨变化相比,精确误差较小,表明该技术具有良好的鉴别能力。我们的数据首次估计了健康软骨中T2整体和局部的再现性误差,可为样本量计算提供依据,并有助于骨关节炎(OA)纵向和横断面试验的研究设计。