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皮肤不同深度的神经支配与小纤维功能相关,但与神经病理性疼痛患者的疼痛无关。

Skin innervation at different depths correlates with small fibre function but not with pain in neuropathic pain patients.

机构信息

Department of Anesthesiology and Intensive Care Medicine, Medical Faculty Mannheim, Heidelberg University, Germany.

出版信息

Eur J Pain. 2012 Nov;16(10):1414-25. doi: 10.1002/j.1532-2149.2012.00157.x. Epub 2012 May 3.

Abstract

BACKGROUND

Neuropathy can lead not only to impaired function but also to sensory sensitization. We aimed to link reduced skin nerve fibre density in different levels to layer-specific functional impairment in neuropathic pain patients and tried to identify pain-specific functional and structural markers.

METHODS

In 12 healthy controls and 36 patients with neuropathic pain, we assessed clinical characteristics, thermal thresholds (quantitative sensory testing) and electrically induced pain and axon reflex erythema. At the most painful sites and at intra-individual control sites, skin biopsies were taken and innervation densities in the different skin layers were assessed. Moreover, neuronal calcitonin gene-related peptide staining was quantified.

RESULTS

Perception of warm, cold and heat pain and nerve fibre density were reduced in the painful areas compared with the control sites and with healthy controls. Warm and cold detection thresholds correlated best with epidermal innervation density, whereas heat and cold pain thresholds and axon reflex flare correlated best with dermal innervation density. Clinical pain ratings correlated only with epidermal nerve fibre density (r = 0.38, p < 0.05) and better preserved cold detection thresholds (r = 0.39, p < 0.05), but not with other assessed functional and structural parameters.

CONCLUSIONS

Thermal thresholds, axon reflex measurements and assessment of skin innervation density are valuable tools to characterize and quantify peripheral neuropathy and link neuronal function to different layers of the skin. The severity of small fibre neuropathy, however, did not correspond to clinical pain intensity and a specific parameter or pattern that would predict pain intensity in peripheral neuropathy could not be identified.

摘要

背景

神经病变不仅会导致功能受损,还会导致感觉过敏。我们旨在将不同水平的皮肤神经纤维密度与神经病理性疼痛患者的特定于层的功能障碍联系起来,并试图确定疼痛特异性的功能和结构标志物。

方法

在 12 名健康对照者和 36 名神经病理性疼痛患者中,我们评估了临床特征、热阈值(定量感觉测试)和电诱导疼痛和轴突反射红斑。在最疼痛的部位和个体内对照部位采集皮肤活检,并评估不同皮肤层的神经支配密度。此外,还对神经元降钙素基因相关肽染色进行了定量。

结果

与对照部位和健康对照组相比,疼痛部位的温暖、寒冷和热痛感知以及神经纤维密度降低。温暖和寒冷的检测阈值与表皮神经支配密度相关性最好,而热和冷痛阈值以及轴突反射红斑与真皮神经支配密度相关性最好。临床疼痛评分仅与表皮神经纤维密度相关(r = 0.38,p < 0.05)和更好地保持冷检测阈值相关(r = 0.39,p < 0.05),但与其他评估的功能和结构参数无关。

结论

热阈值、轴突反射测量和皮肤神经支配密度评估是表征和量化周围神经病变并将神经元功能与皮肤不同层联系起来的有用工具。然而,小纤维神经病变的严重程度与临床疼痛强度不对应,无法确定预测周围神经病变疼痛强度的特定参数或模式。

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