Eajazi Alireza, Weinschenk Cindy, Chhabra Avneesh
Department of Radiology, UT Southwestern Medical Center, Dallas, Texas.
Department of Radiology & Orthopedic Surgery, UT Southwestern Medical Center, Dallas, Texas.
Semin Musculoskelet Radiol. 2024 Feb;28(1):92-102. doi: 10.1055/s-0043-1776427. Epub 2024 Feb 8.
Peripheral neuropathy is a prevalent and debilitating condition affecting millions of individuals globally. Magnetic resonance neurography (MRN) and ultrasonography (US) are noninvasive methods offering comprehensive visualization of peripheral nerves, using anatomical and functional imaging biomarkers to ensure accurate evaluation. For optimized MRN, superior and high-resolution two-dimensional and three-dimensional imaging protocols are essential. The anatomical MRN and US imaging markers include quantitative measures of nerve and fascicular size and signal, and qualitative markers of course and morphology. Among them, quantitative markers of T2-signal intensity ratio are sensitive to nerve edema-like signal changes, and the T1-mapping technique reveals nerve and muscle tissue fatty and fibrous compositional alterations.The functional markers are derived from physiologic properties of nerves, such as diffusion characteristics or blood flow. They include apparent diffusion coefficient from diffusion-weighted imaging and fractional anisotropy and tractography from diffusion tensor imaging to delve into peripheral nerve microstructure and integrity. Peripheral nerve perfusion using dynamic contrast-enhanced magnetic resonance imaging estimates perfusion parameters, offering insights into nerve health and neuropathies involving edema, inflammation, demyelination, and microvascular alterations in conditions like type 2 diabetes, linking nerve conduction pathophysiology to vascular permeability alterations.Imaging biomarkers thus play a pivotal role in the diagnosis, prognosis, and monitoring of nerve pathologies, thereby ensuring comprehensive assessment and elevating patient care. These biomarkers provide valuable insights into nerve structure, function, and pathophysiology, contributing to the accurate diagnosis and management planning for peripheral neuropathy.
周围神经病变是一种普遍且使人衰弱的疾病,影响着全球数百万人。磁共振神经成像(MRN)和超声检查(US)是无创方法,可通过解剖学和功能成像生物标志物对周围神经进行全面可视化,以确保准确评估。为实现优化的MRN,二维和三维的高级高分辨率成像方案至关重要。解剖学MRN和US成像标志物包括神经和束状结构大小及信号的定量测量,以及走行和形态的定性标志物。其中,T2信号强度比的定量标志物对神经水肿样信号变化敏感,而T1映射技术可揭示神经和肌肉组织的脂肪和纤维成分改变。功能标志物源自神经的生理特性,如扩散特征或血流。它们包括扩散加权成像的表观扩散系数以及扩散张量成像的分数各向异性和纤维束成像,以深入研究周围神经的微观结构和完整性。使用动态对比增强磁共振成像的周围神经灌注可估计灌注参数,有助于了解神经健康以及2型糖尿病等疾病中涉及水肿、炎症、脱髓鞘和微血管改变的神经病变,将神经传导病理生理学与血管通透性改变联系起来。因此,成像生物标志物在神经病变的诊断、预后和监测中发挥着关键作用,从而确保全面评估并提升患者护理水平。这些生物标志物为神经结构、功能和病理生理学提供了有价值的见解,有助于周围神经病变的准确诊断和管理规划。