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多发性硬化症中的中枢神经性疼痛是由于胸段脊髓的特定病变引起的。

Central neuropathic pain in MS is due to distinct thoracic spinal cord lesions.

机构信息

UT Southwestern Medical Center, Department of Neurology & Neurotherapeutics, Clinical Center for Multiple Sclerosis Dallas, Texas.

University of Arizona College of Medicine, Phoenix 550 E. Van Buren, Phoenix, Arizona, 85004.

出版信息

Ann Clin Transl Neurol. 2014 Aug;1(8):554-61. doi: 10.1002/acn3.85. Epub 2014 Jul 28.

Abstract

OBJECTIVE

To determine a neuro-anatomic cause for central neuropathic pain (CNP) observed in multiple sclerosis (MS) patients.

METHODS

Parallel clinical and neuro-anatomical studies were performed. A clinical investigation of consecutively acquired MS patients with and without CNP (i.e. cold allodynia or deep hyperesthesia) within a single MS center was pursued. A multivariate logistic regression model was used to assess the relationship between an upper central thoracic spinal cord focus to central pain complaints. To identify the hypothesized autonomic interneurons with bilateral descending projections to lumbosacral sensory neurons, retrograde single- and double-labeling experiments with CTb and fluorescent tracers were performed in three animal species (i.e. rat, cat, and monkey).

RESULTS

Clinical data were available in MS patients with (n = 32; F:23; median age: 34.6 years (interquartile range [IQR]: 27.4-45.5)) and without (n = 30; F:22; median age: 36.6 years [IQR: 31.6-47.1]) CNP. The value of a central focus between T1-T6 in relation to CNP demonstrated a sensitivity of 96.9% (95% confidence interval [CI]: 83.8-99.9) and specificity of 83.3% (95% CI: 65.3-94.4). A significant relationship between CNP and a centrally located focus within the thoracic spine was also observed (odds ratio [OR]: 155.0 [95% CI lower limit: 16.0]; P < 0.0001, two-tailed Fisher exact test). In all animal models, neurons with bilateral descending projections to the lumbosacral superficial dorsal horn were concentrated in the autonomic intermediomedial nucleus surrounding the mid-thoracic central canal.

INTERPRETATION

Our observations provide the first evidence for the etiology of CNP. These data may assist with the development of refined symptomatic therapies and allow for insights into unique pain syndromes observed in other demyelinating subtypes.

摘要

目的

确定多发性硬化症(MS)患者中观察到的中枢神经性疼痛(CNP)的神经解剖学原因。

方法

进行了平行的临床和神经解剖学研究。在单一的 MS 中心,对患有和不患有 CNP(即冷感觉过敏或深部感觉过敏)的连续获得的 MS 患者进行了临床调查。使用多元逻辑回归模型评估上胸段脊髓中央焦点与中央疼痛主诉之间的关系。为了确定具有双侧向腰骶感觉神经元下行投射的假定自主中间神经元,在三个动物物种(即大鼠、猫和猴子)中进行了 CTb 和荧光示踪剂的逆行单标和双标实验。

结果

在患有 CNP 的 MS 患者(n = 32;F:23;中位年龄:34.6 岁(四分位距 [IQR]:27.4-45.5))和不患有 CNP 的 MS 患者(n = 30;F:22;中位年龄:36.6 岁 [IQR:31.6-47.1])中,获得了临床数据。T1-T6 之间中央焦点与 CNP 的相关性的价值显示出 96.9%(95%置信区间 [CI]:83.8-99.9)的敏感性和 83.3%(95% CI:65.3-94.4)的特异性。还观察到 CNP 与胸段脊柱中央部位的焦点之间存在显著的关系(比值比 [OR]:155.0 [95% CI 下限:16.0];P < 0.0001,双侧 Fisher 精确检验)。在所有动物模型中,具有向腰骶部浅层背角双侧下行投射的神经元集中在围绕胸段中央管的自主中间内侧核中。

结论

我们的观察结果为 CNP 的病因提供了第一个证据。这些数据可能有助于开发更精细的对症治疗方法,并深入了解其他脱髓鞘亚型中观察到的独特疼痛综合征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a195/4184558/27ecd477acc3/acn30001-0554-f1.jpg

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