Department of Radiology, Stanford University, RM Lucas Center for Imaging, Stanford, CA, USA.
Neuroimage. 2013 Oct 15;80:234-45. doi: 10.1016/j.neuroimage.2013.05.074. Epub 2013 May 24.
The engineering of a 3 T human MRI scanner equipped with 300 mT/m gradients - the strongest gradients ever built for an in vivo human MRI scanner - was a major component of the NIH Blueprint Human Connectome Project (HCP). This effort was motivated by the HCP's goal of mapping, as completely as possible, the macroscopic structural connections of the in vivo healthy, adult human brain using diffusion tractography. Yet, the 300 mT/m gradient system is well suited to many additional types of diffusion measurements. Here, we present three initial applications of the 300 mT/m gradients that fall outside the immediate scope of the HCP. These include: 1) diffusion tractography to study the anatomy of consciousness and the mechanisms of brain recovery following traumatic coma; 2) q-space measurements of axon diameter distributions in the in vivo human brain and 3) postmortem diffusion tractography as an adjunct to standard histopathological analysis. We show that the improved sensitivity and diffusion-resolution provided by the gradients are rapidly enabling human applications of techniques that were previously possible only for in vitro and animal models on small-bore scanners, thereby creating novel opportunities to map the microstructure of the human brain in health and disease.
配备 300mT/m 梯度的 3T 人体 MRI 扫描仪的工程设计——这是为活体人体 MRI 扫描仪制造的最强梯度——是 NIH 人类连接组计划(HCP)的重要组成部分。这一努力的动机是 HCP 的目标,即使用扩散轨迹描绘尽可能完整地描绘出活体健康成年人大脑的宏观结构连接。然而,300mT/m 梯度系统非常适合许多额外类型的扩散测量。在这里,我们提出了超出 HCP 直接范围的 300mT/m 梯度的三个初始应用。这些包括:1)扩散轨迹描绘以研究意识的解剖结构和创伤性昏迷后大脑恢复的机制;2)活体人脑内轴突直径分布的 q 空间测量和 3)死后扩散轨迹描绘作为标准组织病理学分析的辅助手段。我们表明,梯度提供的灵敏度和扩散分辨率的提高正在迅速实现以前仅在小口径扫描仪上的体外和动物模型上可行的技术的人体应用,从而为在健康和疾病状态下绘制人类大脑的微观结构创造了新的机会。