Concha L
Instituto de Neurobiología, Universidad Nacional Autónoma de México, Mexico.
Neuroscience. 2014 Sep 12;276:14-28. doi: 10.1016/j.neuroscience.2013.09.004. Epub 2013 Sep 17.
Since its introduction in the early 1990s, diffusion-weighted magnetic resonance imaging (MRI) has played a crucial role in the non-invasive evaluation of tissue microstructure of brain parenchyma in vivo. Diffusion anisotropy, in particular, has been extensively used to infer histological changes due to brain maturation and pathology, as it shows a clear dependence on tissue architecture. Although the resolution used in most studies lies in the macroscopic range, the information provided originates at the microscopic level and, as such, diffusion MRI serves as a microscope that can reveal profound details of tissue with direct clinical and research applications. The interpretation of diffusion parameters of white matter rests on what is known to drive diffusion anisotropy, namely axonal membranes, density and coherence, as well as myelin sheaths. However, these factors interact to modulate anisotropy, making interpretations potentially difficult. While there are numerous publications that report diffusion changes in response to particular, histologically confirmed tissue abnormalities in animal models of disease, the microscopic correlates of altered diffusion parameters due to neurological disorders in humans have been difficult to characterize. Animal models may provide insight into the mechanisms involved, but do not necessarily provide accurate representations of the human condition, making human diffusion MRI studies with direct histological confirmation crucial for our understanding of tissue changes secondary to neurodevelopment and disease. This work provides a synopsis of tissue characteristics that give rise to highly informative, specific diffusion patterns, and also of how methodological and artifactual aspects can provide erroneous diffusion measurements that do not accurately reflect tissue and may lead to misinterpretation of results. Examples of diffusion changes due to human conditions are provided to illustrate the wealth of applications of diffusion MRI in clinical and research fields.
自20世纪90年代初引入以来,扩散加权磁共振成像(MRI)在体内对脑实质组织微观结构的无创评估中发挥了关键作用。特别是扩散各向异性,由于其明显依赖于组织结构,已被广泛用于推断因脑成熟和病理导致的组织学变化。尽管大多数研究中使用的分辨率处于宏观范围,但所提供的信息源自微观层面,因此,扩散MRI就像一台显微镜,能够揭示具有直接临床和研究应用价值的组织深层细节。对白质扩散参数的解释取决于已知驱动扩散各向异性的因素,即轴突膜、密度和连贯性以及髓鞘。然而,这些因素相互作用以调节各向异性,使得解释可能变得困难。虽然有许多出版物报道了在疾病动物模型中,特定的、经组织学证实的组织异常所引起的扩散变化,但人类神经系统疾病导致的扩散参数改变的微观相关性一直难以确定。动物模型可能有助于深入了解其中涉及的机制,但不一定能准确反映人类情况,因此,进行具有直接组织学证实的人类扩散MRI研究对于我们理解神经发育和疾病继发的组织变化至关重要。这项工作概述了产生高度信息丰富、特定扩散模式的组织特征,以及方法学和人为因素如何导致错误的扩散测量,这些测量不能准确反映组织情况,可能导致结果的错误解读。文中提供了人类疾病导致的扩散变化实例,以说明扩散MRI在临床和研究领域的广泛应用。