Imaging Strategies To Improve Diagnosis and Treatment of Entrapment Neuropathy

周围神经是存在于动态生物力学环境中的组织良好的复合体组织 由关节的运动产生的。为了适应机械负荷，神经滑动和伸展。 在他们的床上。神经卡压改变了神经的结构，限制了他们的滑行能力，并且过度 增加局部变形，最终损害感觉和运动功能。最常见的 退伍军人中的嵌顿性神经病是腕管综合征(CTS)，这种疾病的中位数是 神经位于腕管内的手腕处。腕管综合征的外科治疗 一般有效，但3%-20%的手术可能需要修改。鉴于CTS的流行，这一点 相当于相当数量的病人。电诊断被认为是 对于CTS的诊断，不确定的结果并不少见，特别是在存在其他重叠的情况下 神经病变，如糖尿病神经病变。 尽管它们可能影响神经病变的进展，但神经结构和生物力学的变化 仅最低限度地用于诊断或追踪神经病，或评估手术治疗的效果。 这在很大程度上是由于使用当前技术对神经进行成像所带来的挑战。我们的 研究小组开发了新的磁共振成像(MRI)和基于超声波的成像方法 这使得神经可以在高空间分辨率的对比度下可视化。这些功能使您能够准确地 神经生物力学(形变和僵硬)的测量，以及识别和定量 神经内部结构元素的特征。这些方法有望提供一种强大的 敏感的非侵入性评估神经病变和手术疗效的方法。 鉴于它的流行，CTS为翻译我们的神经成像和图像提供了一个理想的试验台 将加工技术应用于临床环境。特别是，我们建议使用超声波和核磁共振技术来 评价CTS手术患者正中神经的结构和生物力学。我们的建议 使用多学科方法来解决两个具体目标。我们的首要目标是优化基于MRI的 正中神经的超声成像方法。我们将使用人体身体和活体模型来 验证和优化将用于临床的成像方案。我们预计，基于核磁共振的战略将 提供高分辨率和高对比度的神经结构图像，而超声波将提供快速 神经运动学和僵硬的评估。我们的第二个目标是检查结构和运动学的变化 对CTS患者正中神经在腕管松解前后进行MRI和B超检查。我们 假设基于MRI的成像将检测神经外膜、神经外膜和神经纤维的结构差异 对照神经和被困神经之间的间隔，超声波将检测神经的差异 手术前后对照神经和缠绕神经的变形和僵硬程度。 更广泛地说，我们预计将我们的方法应用于影响退伍军人的其他神经疾病 医疗保健系统，其中的神经结构和生物力学可能被改变。其中包括其他 嵌顿性神经病变、糖尿病神经病变和创伤性神经损伤。最终，成功地执行 我们建议的研究将使我们能够更早地认识到神经病变，提供对神经病变的非侵入性监测 这有助于更准确地评估康复和治疗效果。 1

Peripheral nerves are well-organized composite tissues that exist in a dynamic biomechanical environment created by the movement of articulating joints. To accommodate mechanical loads, nerves glide and stretch within their beds. Nerve entrapment alters the structure of nerves, restricts their ability to glide, and excessively increases regional deformation, ultimately impairing sensory and motor function. The most common entrapment neuropathy among Veterans is carpal tunnel syndrome (CTS), a disease in which the median nerve is impinged at the wrist, within the carpal tunnel. Surgical treatment of carpal tunnel syndrome is generally effective, but revision may be required for 3-20% of surgeries. Given the prevalence of CTS, this corresponds to a substantial number of patients. Electrodiagnostics are considered to be the gold standard for CTS diagnosis, inconclusive outcomes are not uncommon, especially in the presence of other overlying neuropathies, such as diabetic neuropathy. Despite their likely influence on neuropathic progression, nerve structural and biomechanical changes have been used only minimally to diagnose or track neuropathy, or to assess the efficacy of surgical management. This is in large part due to the challenges associated with imaging nerves using current techniques. Our research team has developed new magnetic resonance imaging (MRI) and ultrasound-based imaging methods that allow the visualization of nerves at high spatial resolution on contrast. These capabilities allow accurate measurement of nerve biomechanics (deformation and stiffness), and also identification and quantitative characterization of structural elements within nerves. These methods are expected to provide a powerful and sensitive approach to non-invasively assess neuropathy and surgical efficacy. Given its prevalence, CTS provides an ideal test-bed for translating our nerve imaging and image processing techniques to a clinical setting. In particular, we propose to use ultrasound and MRI techniques to evaluate structure and biomechanics of median nerves in patients requiring surgery for CTS. Our proposal uses a multi-disciplinary approach to address two specific aims. Our first aim is to optimize MRI-based and ultrasound imaging methodology in median nerves. We will use human cadaveric and in vivo models to validate and optimize imaging protocols that will be used clinically. We expect that MRI-based strategies will provide high resolution and high contrast structural images of nerves, while ultrasound will provide rapid assessment of nerve kinematics and stiffness. Our second aim is to examine structural and kinematic changes of median nerves in patients with CTS, before and after carpal tunnel release, using MRI and ultrasound. We hypothesize that MRI-based imaging will detect structural differences in epineurial, perineurial, and nerve fiber compartments between control and entrapped nerves, and ultrasound will detect differences in nerve deformation and stiffness among control nerves and entrapped nerves before and after surgery. More broadly, we anticipate applying our approach to other neurological conditions that impact the Veteran healthcare system, in which nerve structure and biomechanics may be altered. These include other entrapment neuropathies, diabetic neuropathy, and traumatic nerve injury. Ultimately, successful execution of our proposed study will enable earlier recognition of neuropathy, provide noninvasive monitoring of neuropathic progression, and facilitate more accurate assessment of rehabilitative and therapeutic efficacy. 1