Rates of brain atrophy derived from serial magnetic resonance (MR) studies may be used to assess therapies for Alzheimer's disease (AD). These measures may be confounded by changes in scanner voxel sizes. For this reason, the Alzheimer's Disease Neuroimaging Initiative (ADNI) included the imaging of a geometric phantom with every scan. This study compares voxel scaling correction using a phantom with correction using a 9 degrees of freedom (9DOF) registration algorithm. We took 129 pairs of baseline and 1-year repeat scans, and calculated the volume scaling correction, previously measured using the phantom. We used the registration algorithm to quantify any residual scaling errors, and found the algorithm to be unbiased, with no significant (p=0.97) difference between control (n=79) and AD subjects (n=50), but with a mean (SD) absolute volume change of 0.20 (0.20) % due to linear scalings. 9DOF registration was shown to be comparable to geometric phantom correction in terms of the effect on atrophy measurement and unbiased with respect to disease status. These results suggest that the additional expense and logistic effort of scanning a phantom with every patient scan can be avoided by registration-based scaling correction. Furthermore, based upon the atrophy rates in the AD subjects in this study, sample size requirements would be approximately 10-12% lower with (either) correction for voxel scaling than if no correction was used.

译文

来自连续磁共振 (MR) 研究的脑萎缩率可用于评估阿尔茨海默氏病 (AD) 的治疗方法。这些措施可能会因扫描仪体素大小的变化而混淆。因此,阿尔茨海默氏病神经成像计划 (ADNI) 每次扫描都包括几何体模的成像。本研究比较了使用体模的体素缩放校正与使用9自由度 (9DOF) 配准算法的校正。我们进行了129对基线和1年重复扫描,并计算了先前使用体模测量的体积缩放校正。我们使用配准算法来量化任何残余缩放误差,发现该算法是无偏的,对照 (n = 79) 和AD受试者 (n = 50) 之间没有显着 (p = 0.97) 差异,但由于线性定标,平均 (SD) 绝对体积变化为0.20 (0.20) %。就萎缩测量的影响而言,9DOF配准与几何体模校正相当,并且在疾病状态方面没有偏见。这些结果表明,通过基于配准的缩放校正可以避免每次患者扫描时扫描幻影的额外费用和后勤工作。此外,基于本研究中AD受试者的萎缩率,与不使用校正的情况相比,使用 (任一) 体素标度校正的样本量要求将低约10-12%。

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