McConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, 3801 University Street, Montreal, Quebec, Canada H3A 2B4.
Neuroimage. 2010 Jan 15;49(2):1601-11. doi: 10.1016/j.neuroimage.2009.08.008. Epub 2009 Aug 12.
Precise and accurate quantification of whole-brain atrophy based on magnetic resonance imaging (MRI) data is an important goal in understanding the natural progression of neurodegenerative disorders such as Alzheimer's disease and multiple sclerosis. We found that inconsistent MRI positioning of subjects is common in typically acquired clinical trial data - particularly along the magnet's long (i.e., Z) axis. We also found that, if not corrected for, the gradient distortion effects associated with such Z-shifts can significantly decrease the accuracy and precision of MRI-derived measures of whole-brain atrophy - negative effects that increase in magnitude with (i) increases in the Z-distance between the brains to be compared and (ii) increases in the Z-distance from magnet isocenter of the center of the pair of brains to be compared. These gradient distortion effects can be reduced by accurate subject positioning, and they can also be corrected post hoc with the use of appropriately-generated gradient-distortion correction fields. We used a novel DUPLO-based phantom to develop a spherical-harmonics-based gradient distortion field that was used to (i) correct for observed Z-shift-associated gradient distortion effects on SIENA-generated measures of brain atrophy and (ii) simulate the gradient distortion effects that might be expected with a greater range of Z-shifts than those that we were able to acquire. Our results suggest that consistent alignment to magnet isocenter and/or correcting for the observed effects of gradient distortion should lead to more accurate and precise estimates of brain-related changes and, as a result, to increased statistical power in studies aimed at understanding the natural progression and the effective treatment of neurodegenerative disorders.
基于磁共振成像 (MRI) 数据准确而精确地量化全脑萎缩是理解阿尔茨海默病和多发性硬化症等神经退行性疾病自然进程的重要目标。我们发现,在典型的临床研究数据中,受试者的 MRI 定位不一致是很常见的——特别是沿着磁体的长轴(即 Z 轴)。我们还发现,如果不加以纠正,与这种 Z 偏移相关的梯度失真效应会显著降低基于 MRI 的全脑萎缩测量的准确性和精密度——这些负面影响随着(i)要比较的大脑之间的 Z 距离的增加和(ii)要比较的大脑中心与磁体等中心之间的 Z 距离的增加而增大。这些梯度失真效应可以通过准确的受试者定位来减少,也可以使用适当生成的梯度失真校正场在事后进行校正。我们使用一种新颖的基于 DUPLO 的仿体来开发基于球谐的梯度失真校正场,用于(i)校正 SIENA 生成的脑萎缩测量值中与观察到的 Z 偏移相关的梯度失真效应,以及(ii)模拟比我们能够获得的更大范围的 Z 偏移可能预期的梯度失真效应。我们的结果表明,一致地对齐到磁体等中心和/或校正观察到的梯度失真效应,应该会导致更准确和精确的脑相关变化估计,从而在旨在理解神经退行性疾病的自然进程和有效治疗的研究中提高统计能力。