摘要
目的观察复发性视神经炎的临床特点以及自身免疫抗体(水通道蛋白4抗体和血清抗核抗体)的分布。方法收集2010年10月至2012年4月间在解放军总医院神经眼科住院诊治的复发性视神经炎患者54例的临床资料,回顾分析其一般临床特点,统计其水通道蛋白4抗体(AQP4-Ab)(36例)和血清抗核抗体(ANAs)的阳性率,并与相关文献数据分析比较。结果男女比例1:2.6,发病年龄平均30.3岁;病程50d~20年,发病次数2。8次。病程中最差视力(矫正后)在0.1以下者44例,占81.5%。ANAs阳性率22.2%(12/54),AQP4-Ab阳性率27.8%(10/36);颅脑和,或脊髓核磁异常者占48.0%(24/50);脑脊液异常70.0%(16/23)。结论复发性视神经炎多发于青壮年,视力损害较重,自身免疫抗体(AQP4-Ab和ANAs)阳性率较视神经脊髓炎及复发性长节段横贯性脊髓炎略低,中枢神经系统影像检查对其诊治有重要价值。
ObJective To investigate the clinical features and seroprevalence of autoimmune antibodies (aquaporin-4 antibodies, AQP4-Ab and antinucl^ar antibodies, ANAs) in patients with recurrent optic neuritis (RON). Methods Fifty-four RON patients who were in -hospital in Ophthalmolo- gy Department of PLA from October 2010 to April 2012 were enrolled in the study. The general clinical features and statistic the positive rate of AQP4-Ab and ANAs were analyzed retrospectively, and the relative data in other studies were compared. Results The ratio of male to female was 1: 2.6 and the average age of onset was 30.3 years old. The recurrent attacks of optic neuritis were 2 to 8 times during 50 days to 20 years. There were 44 patients (81.5%) who had ever appeared the lowest visual acuity (corrected) of 〈0.1 in the course of disease. The rate of seropositive ANAs was 22.2% (12/54) while 27.8% (10/36) for AQP4-Ab. The 48.0% (24/50) cases were abnormal in Brain and/or spinal cord MRI and 70.0% (16/23) in CSF. Conclusions RON is more appeared in youth with poor visual acuity. The positive rate of AQP4-Ab and ANAs are lower than neuromyelitis optica (NMO) and recurrent longitudinally extensive transverse myelitis (r-LETM). The MRI of central nervous system posses important value for diagnosis and treatment of RON.
出处
《中国实用眼科杂志》
CSCD
北大核心
2013年第3期346-349,共4页
Chinese Journal of Practical Ophthalmology