Department of Neurology, Children's National Medical Center, Washington, D.C. 20010, USA.
Mol Genet Metab. 2011 Nov;104(3):195-205. doi: 10.1016/j.ymgme.2011.06.020. Epub 2011 Jun 30.
Most inborn errors of metabolism (IEMs) are associated with potential for injury to the developing central nervous system resulting in chronic encephalopathy, though the etiopathophysiology of neurological injury have not been fully established in many disorders. Shared mechanisms can be envisioned such as oxidative injury due to over-activation of N-Methyl-d-Aspartate (NMDA) receptors with subsequent glutamatergic damage, but other causes such as energy depletion or inflammation are possible. Neuroimaging has emerged as a powerful clinical and research tool for studying the brain in a noninvasive manner. Several platforms exist to study neural networks underlying cognitive processes, white matter/myelin microstructure, and cerebral metabolism in vivo. The scope and limitations of these methods will be discussed in the context of valuable information they provide in the study and management of selected inborn errors of metabolism. This review is not meant to be an exhaustive coverage of diagnostic findings on MRI in multiple IEMs, but rather to illustrate how neuroimaging modalities beyond T1 and T2 images, can add depth to an understanding of the underlying brain changes evoked by the selected IEMs. Emphasis will be placed on techniques that are available in the clinical setting. Though technically complex, many of these modalities have moved - or soon will - to the clinical arena.
大多数先天性代谢缺陷(IEMs)都与潜在的中枢神经系统发育损伤有关,导致慢性脑病,尽管许多疾病的神经损伤的病因和发病机制尚未完全确定。可以设想一些共同的机制,如 NMDA 受体过度激活引起的氧化损伤,随后发生谷氨酸能损伤,但也可能有其他原因,如能量耗竭或炎症。神经影像学已成为一种强大的临床和研究工具,用于非侵入性地研究大脑。目前有几种平台可用于研究认知过程、白质/髓鞘微观结构和体内大脑代谢的神经网络。将讨论这些方法的范围和局限性,以及它们在选定的先天性代谢缺陷的研究和管理中提供的有价值的信息。本综述并非旨在全面涵盖多种先天性代谢缺陷的 MRI 诊断结果,而是旨在说明 T1 和 T2 图像以外的神经影像学方式如何深入了解所选先天性代谢缺陷引起的潜在脑变化。重点将放在临床环境中可用的技术上。尽管技术上很复杂,但其中许多方式已经或即将进入临床领域。