病例报告:利用弥散加权MRI对脊髓刺激治疗的慢性腰痛患者进行检查。

Isaiah Ailes, Mashaal Syed, Caio M Matias, Laura Krisa, Jingya Miao, Anish Sathe, Islam Fayed, Abdulaziz Alhussein, Peter Natale, Feroze B Mohamed, Kiran Talekar, Mahdi Alizadeh
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摘要

扩散加权磁共振成像(dwMRI)在分析神经元微观结构方面的应用越来越广泛。在慢性腰痛(cLBP)患者中,使用dwMRI观察神经元微观结构可以获得非侵入性的生物标志物,为临床医生提供客观的定量预后工具。在本病例报告中,我们通过对一名接受脊髓刺激(SCS)治疗的55岁男性背部手术综合征(FBSS)患者进行基于区域的分析,研究了dwMRI对非侵入性生物标志物的开发。我们假设dwMRI可以安全地生成反映神经调节驱动的大脑微观结构改变的定量数据。在scs植入后6个月和12个月进行神经影像学检查。生成的定量图包括扩散张量成像(DTI)参数;分数各向异性(FA)、轴向扩散率(AD)、径向扩散率(RD)和平均扩散率(MD)由全脑导管造影计算。为了检查大脑的特定区域,提取44个感兴趣区域(roi),共同代表疼痛神经基质,并将其注册到患者的扩散空间。根据6个月和12个月的roi计算平均扩散指数。在4幅地图中,至少有3幅报告了相对变化>10%的地区。使用此选择标准,8个roi显示出超过10%的相对变化。这些roi主要位于岛回。除了定量数据外,在6个月和12个月的访问期间,还进行了一系列问卷调查,以评估疼痛强度、功能残疾和生活质量。在这些成分中观察到总体改善,其中疼痛灾难量表(PCS)显示出最大的变化。最后,我们证明了dwMRI对SCS患者的安全性。总之,该病例报告的结果提示在更大的队列中应用dwMRI进行进一步的研究,以更好地将SCS的影响与脑微结构改变联系起来,支持dwMRI在产生非侵入性生物标志物用于预测方面的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Case report: Utilizing diffusion-weighted MRI on a patient with chronic low back pain treated with spinal cord stimulation.

Diffusion-weighted magnetic resonance imaging (dwMRI) has increasingly demonstrated greater utility in analyzing neuronal microstructure. In patients with chronic low back pain (cLBP), using dwMRI to observe neuronal microstructure can lead to non-invasive biomarkers which could provide clinicians with an objective quantitative prognostic tool. In this case report, we investigated dwMRI for the development of non-invasive biomarkers by conducting a region-based analysis of a 55-year-old male patient with failed back surgery syndrome (FBSS) treated with spinal cord stimulation (SCS). We hypothesized that dwMRI could safely generate quantitative data reflecting cerebral microstructural alterations driven by neuromodulation. Neuroimaging was performed at 6- and 12- months post-SCS implantation. The quantitative maps generated included diffusion tensor imaging (DTI) parameters; fractional anisotropy (FA), axial diffusivity (AD), radial diffusivity (RD), and mean diffusivity (MD) computed from whole brain tractography. To examine specific areas of the brain, 44 regions of interest (ROIs), collectively representing the pain NeuroMatrix, were extracted and registered to the patient's diffusion space. Average diffusion indices were calculated from the ROIs at both 6- and 12- months. Regions with >10% relative change in at least 3 of the 4 maps were reported. Using this selection criterion, 8 ROIs demonstrated over 10% relative changes. These ROIs were mainly located in the insular gyri. In addition to the quantitative data, a series of questionnaires were administered during the 6- and 12-month visits to assess pain intensity, functional disability, and quality of life. Overall improvements were observed in these components, with the Pain Catastrophizing Scale (PCS) displaying the greatest change. Lastly, we demonstrated the safety of dwMRI for a patient with SCS. In summary, the results from the case report prompt further investigation in applying dwMRI in a larger cohort to better correlate the influence of SCS with brain microstructural alterations, supporting the utility of dwMRI to generate non-invasive biomarkers for prognostication.

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