Kosmidis Michalis L, Koutsogeorgopoulou Loukia, Alexopoulos Harry, Mamali Ioanna, Vlachoyiannopoulos Panagiotis G, Voulgarelis Michalis, Moutsopoulos Haralampos M, Tzioufas Athanasios G, Dalakas Marinos C
Neuroimmunology Unit, Department of Pathophysiology, Faculty of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Neuroimmunology Unit, Department of Pathophysiology, Faculty of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
J Neurol Sci. 2014 Dec 15;347(1-2):143-7. doi: 10.1016/j.jns.2014.09.035. Epub 2014 Sep 28.
Fibromyalgia (FM) is one of the most common chronic pain syndromes. Various pathogenetic mechanisms have been implicated but none is proven. Our scope was to determine if Intraepidermal Nerve Fiber Density (IENFD) is reduced in the skin of FM patients, as observed in patients with painful small fiber sensory neuropathy (SFSN).
DESIGN, SETTING AND PARTICIPANTS: We prospectively studied 46 FM patients (5 men and 41 women), aged 29 to 76 (mean: 52.5) years, diagnosed according to the ACR 2010 criteria, and 34 controls (18 women and 16 men) aged 19 to 84 (mean: 31.7) years. IENFD was measured using published guidelines and immune markers were sought immunocytochemically. In 30 FM patients, pain intensity was assessed with the Neuropathic Pain Symptom Inventory (NPSI), a scale validated for neuropathic pain.
15 of 46 (32.6%) FM patients had reduced IENFD [range: 0.6-12.5 fibers/mm (mean: 4.83 SD: 2.5)], compared to healthy controls [2.8-11.5 fibers/mm (mean: 7.35, SD: 1.85)] (p<0.0001). No significant correlation was noticed between NPSI scores and IENFD. No difference in the Langerhans cells, the major Antigen Presenting Cells (APCs) in the epidermis, or in IL-6 staining, was noted between FM and controls. IENFD was equally reduced in a subset of FM patients who also had another autoimmune disease.
This is one of the largest series of FM patients demonstrating a significant reduction of IENFD in their skin biopsies. The findings indicate that in a subset of FM patients, the pain syndrome is, at least partially, of neuropathic origin. Skin biopsy may prove a useful tool and a potential biomarker in future studies of FM patients.
纤维肌痛(FM)是最常见的慢性疼痛综合征之一。虽然有多种发病机制被提出,但均未得到证实。我们的研究目的是确定FM患者皮肤中的表皮内神经纤维密度(IENFD)是否如疼痛性小纤维感觉神经病变(SFSN)患者那样降低。
设计、地点和参与者:我们前瞻性地研究了46例FM患者(5名男性和41名女性),年龄在29至76岁(平均52.5岁),根据美国风湿病学会(ACR)2010标准确诊,以及34名对照者(18名女性和16名男性),年龄在19至84岁(平均31.7岁)。使用已发表的指南测量IENFD,并通过免疫细胞化学方法寻找免疫标志物。在30例FM患者中,使用神经病理性疼痛症状量表(NPSI)评估疼痛强度,该量表已被验证可用于评估神经病理性疼痛。
46例FM患者中有15例(32.6%)IENFD降低[范围:每毫米0.6 - 12.5条纤维(平均:4.83,标准差:2.5)],而健康对照者为[每毫米2.8 - 11.5条纤维(平均:7.35,标准差:1.85)](p<0.0001)。未发现NPSI评分与IENFD之间存在显著相关性。在FM患者和对照者之间,未观察到表皮中主要抗原呈递细胞(APC)朗格汉斯细胞或白细胞介素-6染色有差异。在患有另一种自身免疫性疾病的FM患者亚组中,IENFD同样降低。
这是最大规模的FM患者系列研究之一,证明其皮肤活检中IENFD显著降低。研究结果表明,在一部分FM患者中,疼痛综合征至少部分源于神经病变。皮肤活检可能是未来FM患者研究中的有用工具和潜在生物标志物。