Gøransson Lasse G, Brun Johan G, Harboe Erna, Mellgren Svein I, Omdal Roald
Clinical Immunology Unit, Department of Internal Medicine, Stavanger University Hospital, Stavanger, Norway.
Arch Neurol. 2006 Oct;63(10):1410-3. doi: 10.1001/archneur.63.10.1410.
Some patients with systemic lupus erythematosus have selective loss of small-diameter nerve fibers, while larger nerve fibers are unaffected.
To determine intraepidermal nerve fiber densities in patients with different chronic inflammatory autoimmune diseases.
Cross-sectional study.
Stavanger University Hospital, Stavanger, and Haukeland University Hospital, Haukeland, Norway.
Sixty patients with systemic lupus erythematosus (SLE) (mean +/- SD age, 43.2 +/- 13.5 years), 61 patients with primary Sjögren syndrome (age, 57.1 +/- 14.7 years), and 52 patients with rheumatoid arthritis (age, 57.4 +/- 12.3 years) were compared with 106 healthy subjects (age, 49.0 +/- 19.6 years).
Skin biopsy specimens.
To evaluate small-diameter nerve fiber loss, intraepidermal nerve fiber densities were measured in skin punch biopsy specimens obtained from the distal part of the leg.
The mean +/- SD densities were 7.5 +/- 3.8 fibers/mm in patients with SLE, 9.2 +/- 3.8 fibers/mm in primary Sjögren syndrome, and 10.9 +/- 5.4 fibers/mm in rheumatoid arthritis vs 12.4 +/- 4.6 fibers/mm in healthy subjects. Densities were significantly less in patients with SLE vs patients with rheumatoid arthritis and vs healthy subjects (P<.001 for both), as well as in patients with primary Sjögren syndrome vs healthy subjects (P<.001). Eight patients (13%) with SLE, 2 patients (3%) with primary Sjögren syndrome, and 2 patients (4%) with rheumatoid arthritis had densities below the lower reference limit of 3.4 fibers/mm, consistent with small-diameter nerve fiber neuropathy.
The degree of loss of small-diameter nerve fibers differs among patients with these chronic inflammatory autoimmune diseases, likely reflecting differences in pathogenesis and organ affinity of the individual disease entities.
一些系统性红斑狼疮患者存在小直径神经纤维选择性缺失,而较大直径神经纤维未受影响。
确定不同慢性炎症性自身免疫病患者的表皮内神经纤维密度。
横断面研究。
挪威斯塔万格的斯塔万格大学医院和豪克兰的豪克兰大学医院。
60例系统性红斑狼疮(SLE)患者(平均±标准差年龄,43.2±13.5岁)、61例原发性干燥综合征患者(年龄,57.1±14.7岁)和52例类风湿关节炎患者(年龄,57.4±12.3岁),与106名健康受试者(年龄,49.0±19.6岁)进行比较。
皮肤活检标本。
为评估小直径神经纤维缺失情况,在取自小腿远端的皮肤打孔活检标本中测量表皮内神经纤维密度。
SLE患者的平均±标准差密度为7.5±3.8条纤维/mm,原发性干燥综合征患者为9.2±3.8条纤维/mm,类风湿关节炎患者为10.9±5.4条纤维/mm,而健康受试者为12.4±4.6条纤维/mm。SLE患者的密度显著低于类风湿关节炎患者和健康受试者(两者P均<0.001),原发性干燥综合征患者与健康受试者相比密度也显著降低(P<0.001)。8例(13%)SLE患者、2例(3%)原发性干燥综合征患者和2例(4%)类风湿关节炎患者的密度低于3.4条纤维/mm的下限参考值,符合小直径神经纤维神经病变。
这些慢性炎症性自身免疫病患者中小直径神经纤维的缺失程度不同,这可能反映了个体疾病实体在发病机制和器官亲和力方面的差异。