颈椎病脊髓弥散张量成像:可量化标记物在手术减压评估中的初步研究

Matthew M. Kang, Erich G. Anderer, Robert E. Elliott, S. Kalhorn, P. Cooper, A. Frempong-Boadu, S. M. Hesseltine, Y. Ge, Joshua Marcus, M. Law
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引用次数: 10

摘要

目的:常规MRI评估脊髓型颈椎病(CSM)可能与患者的症状和预后相关性较差。对椎管狭窄、轮廓畸形和T2信号有无改变的解释,可能使患者难以决定是否需要进行减压手术。弥散张量成像(DTI)提供定量测量,可以帮助阐明退行性颈椎病压迫脊髓疾病的程度和慢性。DTI还可以检测急性脊柱炎受压区弥散异常,而T2信号无变化。本研究的目的是比较有严重临床和影像学证据的CSM患者与对照组的定量DTI测量(即指标)。方法:采用脉冲梯度、双旋回波、回波平面成像技术,对11例计划行手术减压的严重影像学和临床多节段颈椎病患者与10名健康志愿者(由2名神经外科医生A.F.B.和p.r.c.以及1名神经放射学家M.L.确定)进行颈椎DTI检查。在C2-3、C3-4和C4-5水平,计算双侧脊髓前部、外侧和后部感兴趣区域内的平均FA、MD、E1(纵向扩散)、E2和E3(横向扩散)。由于DTI上的伪影,未分析C4-5尾部的水平。颈椎病患者的平均年龄为67.2±9.8岁,对照组为33.4±15.2岁(p< 0.001)。结果:分数各向异性(FA)和次要横向特征值(E2和E3)最一致地显示了放射学和临床CSM患者与对照组在C4-5处的显著差异。在C4-5的常规T2成像上,FA与压迫的相关性最强;然而,与对照组相比,次要特征值在DTI指标上显示出最大程度的显著差异。在C2-3时,平均扩散率(MD)在外侧和中心区域有显著差异,在后部、外侧和中心区域有较小的特征值差异。CSM患者与对照组的主要纵向特征值(E1)无显著差异。结论:小特征值和分数各向异性在临床明显的颈椎病中有显著差异,常规影像学证据表明压迫与对照组相比,主要特征值保持不变。这些值显示了作为脊髓显微损伤的生物标志物的前景,这可能有助于早期识别可能从减压治疗中受益的患者。DTI还可以提供脊髓受压持续时间的信息,以帮助区分可逆性和不可逆性疾病。资助:国家癌症研究所/国家卫生研究所RO1CA093992和RO1111996基金。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diffusion Tensor Imaging of the Spondylotic Cervical Spinal Cord: A Preliminary Study of Quantifiable Markers in the Evaluation for Surgical Decompression
Objective: Conventional MRI for the evaluation of cervical spondylotic myelopathy (CSM) may be poorly correlated with a patient’s symptoms and prognosis. Interpretation of canal stenosis, contour deformities, and the presence or absence of T2 signal change, can make it difficult to decide who needs decompressive surgery. Diffusion tensor imaging (DTI) provides quantitative measurements that could help clarify the degree and chronicity of spinal cord disease as a result of compression from degenerative spondylosis. DTI can also detect diffusion abnormalities in areas of acute spondylotic compression occurring without T2 signal change. The purpose of this study is to compare these quantitative DTI measures (i.e. metrics) in patients with severe clinical and radiographic evidence of CSM with controls. Methods: DTI of the cervical spine was performed in 11 patients with severe radiographic and clinical multilevel spondylosis who were planned for surgical decompression versus 10 healthy volunteers (as determined by 2 neurosurgeons A.F.B. and P.R.C., and a neuroradiologist M.L.), using pulsed gradient, double spin echo, echo planar imaging. At the C2-3, C3-4 and C4-5 levels, average FA, MD, E1 (longitudinal diffusion), E2 and E3 (transverse diffusion) were calculated within regions of interest at bilateral anterior, lateral, and posterior regions of the cord. Levels caudal to C4-5 were not analyzed due to artifact on DTI. The average age of the spondylosis patients was 67.2±9.8 years vs. 33.4±15.2 years in the control group (p<.001). Results: Fractional anisotropy (FA) and the minor transverse eigenvalues (E2 and E3) most consistently demonstrated significant differences in values between patients with radiographic and clinical CSM versus controls at C4-5. FA was the most specific in correlating with compression seen on conventional T2 imaging at C4-5; however, the minor eigenvalues showed the greatest degree of significant difference in DTI metrics when compared to controls. At C2-3, significant differences in mean diffusivity (MD) were found at the lateral and central regions as well as minor eigenvalue differences in the posterior, lateral, and central regions. There were no significant differences in the major longitudinal eigenvalue (E1) between patients with CSM versus controls. Conclusion: Minor eigenvalues and fractional anisotropy are significantly different in clinically significant spondylosis with conventional imaging evidence of compression versus controls, with preservation of the major eigenvalue. These values show promise as biomarkers of microscopic injury to the cord, which may help in the early identification of patients who would likely benefit from decompressive therapy. DTI can also provide information on the duration of cord compression in helping to distinguish reversible versus irreversible disease. Supported by: Grants RO1CA093992 and RO1111996 from the National Cancer Institute/National Institute of Health.
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