Dortch Richard D, Dethrage Lindsey M, Gore John C, Smith Seth A, Li Jun
From the Department of Radiology and Radiological Sciences (R.D.D., J.C.G., S.A.S.), Vanderbilt University Institute of Imaging Science (R.D.D., L.M.D., J.C.G., S.A.S.), and the Departments of Biomedical Engineering (R.D.D., J.C.G., S.A.S.), Physics and Astronomy (J.C.G., S.A.S.), Molecular Physiology and Biophysics (J.C.G.), and Neurology (J.L.), Vanderbilt University, Nashville, TN.
Neurology. 2014 Oct 21;83(17):1545-53. doi: 10.1212/WNL.0000000000000919. Epub 2014 Sep 24.
The objectives of this study were (1) to develop a novel magnetization transfer ratio (MTR) MRI assay of the proximal sciatic nerve (SN), which is inaccessible via current tools for assessing peripheral nerves, and (2) to evaluate the resulting MTR values as a potential biomarker of myelin content changes in patients with Charcot-Marie-Tooth (CMT) diseases.
MTR was measured in the SN of patients with CMT type 1A (CMT1A, n = 10), CMT type 2A (CMT2A, n = 3), hereditary neuropathy with liability to pressure palsies (n = 3), and healthy controls (n = 21). Additional patients without a genetically confirmed subtype (n = 4), but whose family histories and electrophysiologic tests were consistent with CMT, were also included. The relationship between MTR and clinical neuropathy scores was assessed, and the interscan and inter-rater reliability of MTR was estimated.
Mean volumetric MTR values were significantly decreased in the SN of patients with CMT1A (33.8 ± 3.3 percent units) and CMT2A (31.5 ± 1.9 percent units) relative to controls (37.2 ± 2.3 percent units). A significant relationship between MTR and disability scores was also detected (p = 0.01 for genetically confirmed patients only, p = 0.04 for all patients). From interscan and inter-rater reliability analyses, proximal nerve MTR values were repeatable at the slicewise and mean volumetric levels.
MTR measurements may be a viable biomarker of proximal nerve pathology in patients with CMT.
本研究的目的是:(1)开发一种新型的磁化传递率(MTR)磁共振成像(MRI)检测方法,用于检测目前评估周围神经的工具无法触及的坐骨神经近端;(2)评估所得的MTR值,将其作为夏科-马里-图斯(CMT)病患者髓鞘含量变化的潜在生物标志物。
对10例1A型CMT(CMT1A)患者、3例2A型CMT(CMT2A)患者、3例遗传性压力易感性周围神经病患者以及21名健康对照者的坐骨神经近端进行MTR测量。还纳入了4例未经过基因确诊亚型,但家族史和电生理检查结果与CMT相符的患者。评估MTR与临床神经病变评分之间的关系,并估计MTR的扫描间和评分者间可靠性。
相对于对照组(37.2±2.3%单位),CMT1A患者(33.8±3.3%单位)和CMT2A患者(31.5±1.9%单位)坐骨神经近端的平均体积MTR值显著降低。还检测到MTR与残疾评分之间存在显著关系(仅基因确诊患者p = 0.01,所有患者p = 0.04)。通过扫描间和评分者间可靠性分析,近端神经MTR值在层面和平均体积水平上具有可重复性。
MTR测量可能是CMT患者近端神经病变的一种可行生物标志物。