Doppler Kathrin, Rittner Heike L, Deckart Maximiliane, Sommer Claudia
Department of Neurology, University Hospital Würzburg, Würzburg, Germany Department of Anesthesia and Critical Care, Interdisciplinary Pain Clinic, University Hospital Würzburg, Würzburg, Germany Schmerzklinik am Arkauwald, Bad Mergentheim, Germany.
Pain. 2015 Nov;156(11):2319-2325. doi: 10.1097/j.pain.0000000000000285.
Recent studies have provided evidence of pathology and functional abnormalities of small nerve fibers as a potential correlate of pain in the fibromyalgia syndrome. Here, we aimed to quantify dermal unmyelinated nerve fiber diameter at the electron microscopic level to find a potential morphological correlate of the functional disturbance. Thirty-two patients with fibromyalgia syndrome, 12 patients with small fiber neuropathy, and 24 healthy controls were prospectively recruited. Skin biopsies of the distal and proximal legs and index finger were taken and processed for immunofluorescence and for electron microscopy. We determined the diameter of small unmyelinated nerve fibers by measuring ten transversely cut axons of each biopsy. The mean axon diameter was reduced in patients with fibromyalgia syndrome compared with patients with small fiber neuropathy and controls (P < 0.05). Furthermore, we confirmed previous findings of disturbed small fiber function in quantitative sensory testing and of reduced intraepidermal nerve fiber density in patients with fibromyalgia. Our study provides further evidence of small fiber pathology in fibromyalgia syndrome and discloses differences compared with small fiber neuropathy, indicating that different pathomechanisms may lead to small fiber loss in the 2 disorders.
近期研究已证实,小神经纤维的病理学及功能异常可能与纤维肌痛综合征中的疼痛相关。在此,我们旨在通过电子显微镜水平量化真皮无髓神经纤维直径,以寻找功能障碍的潜在形态学关联。前瞻性招募了32例纤维肌痛综合征患者、12例小纤维神经病变患者及24名健康对照者。采集远端和近端腿部以及食指的皮肤活检样本,进行免疫荧光和电子显微镜处理。通过测量每个活检样本中十条横切轴突来确定小无髓神经纤维的直径。与小纤维神经病变患者及对照者相比,纤维肌痛综合征患者的平均轴突直径减小(P < 0.05)。此外,我们证实了先前在定量感觉测试中关于纤维肌痛综合征患者小纤维功能障碍以及表皮内神经纤维密度降低的研究结果。我们的研究进一步证明了纤维肌痛综合征中存在小纤维病理学,并揭示了与小纤维神经病变的差异,表明不同的发病机制可能导致这两种疾病中的小纤维丢失。