Nakajima Hideki, Motomura Masakatsu, Tanaka Keiko, Fujikawa Azusa, Nakata Ruka, Maeda Yasuhiro, Shima Tomoaki, Mukaino Akihiro, Yoshimura Shunsuke, Miyazaki Teiichiro, Shiraishi Hirokazu, Kawakami Atsushi, Tsujino Akira
Unit of Translational Medicine, Department of Neurology and Strokology, Nagasaki University Hospital, Nagasaki, Japan.
Unit of Translational Medicine, Department of Neurology and Strokology, Nagasaki University Hospital, Nagasaki, Japan Faculty of Engineering Department of Engineering, Medical Engineering Course, Nagasaki Institute of Applied Science, Nagasaki, Japan.
BMJ Open. 2015 Apr 2;5(4):e007766. doi: 10.1136/bmjopen-2015-007766.
To investigate the differences of clinical features, cerebrospinal fluid (CSF), MRI findings and response to steroid therapies between patients with optic neuritis (ON) who have myelin oligodendrocyte glycoprotein (MOG) antibodies and those who have seronegative ON.
We recruited participants in the department of neurology and ophthalmology in our hospital in Japan.
We retrospectively evaluated the clinical features and response to steroid therapies of patients with ON. Sera from patients were tested for antibodies to MOG and aquaporin-4 (AQP4) with a cell-based assay.
Between April 2009 and March 2014, we enrolled serial 57 patients with ON (27 males, 30 females; age range 16-84 years) who ophthalmologists had diagnosed as having or suspected to have ON with acute visual impairment and declined critical flicker frequency, abnormal findings of brain MRI, optical coherence tomography and fluorescein fundus angiography at their onset or recurrence. We excluded those patients who fulfilled the diagnostic criteria of neuromyelitis optica (NMO)/NMO spectrum disorders (NMOSD), MS McDonald's criteria, and so on. Finally we defined 29 patients with idiopathic ON (14 males, 15 females, age range 16-84 years).
27.6% (8/29) were positive for MOG antibodies and 3.4% (1/29) were positive for AQP4. Among the eight patients with MOG antibodies, five had optic pain (p=0.001) and three had prodromal infection (p=0.179). Three of the eight MOG-positive patients showed significantly high CSF levels of myelin basic protein (p=0.021) and none were positive for oligoclonal band in CSF. On MRIs, seven MOG-positive patients showed high signal intensity on optic nerve, three had a cerebral lesion and one had a spinal cord lesion. Seven of the eight MOG-positive patients had a good response to steroid therapy.
Although not proving primary pathogenicity of anti-MOG antibodies, the present results indicate that the measurement of MOG antibodies is useful in diagnosing and treating ON.
研究髓鞘少突胶质细胞糖蛋白(MOG)抗体阳性的视神经炎(ON)患者与血清学阴性的ON患者在临床特征、脑脊液(CSF)、磁共振成像(MRI)表现及对类固醇治疗反应方面的差异。
我们在日本我院神经内科和眼科招募参与者。
我们回顾性评估了ON患者的临床特征及对类固醇治疗的反应。采用基于细胞的检测方法检测患者血清中的MOG抗体和水通道蛋白4(AQP4)抗体。
2009年4月至2014年3月期间,我们连续纳入了57例ON患者(男27例,女30例;年龄范围16 - 84岁),这些患者经眼科医生诊断为患有或疑似患有ON伴急性视力损害,且在发病或复发时临界闪烁频率下降、脑MRI、光学相干断层扫描及荧光素眼底血管造影有异常表现。我们排除了符合视神经脊髓炎(NMO)/NMO谱系障碍(NMOSD)、MS McDonald标准等诊断标准的患者。最终确定29例特发性ON患者(男14例,女15例,年龄范围16 - 84岁)。
29例患者中,27.6%(8/29)MOG抗体阳性,3.4%(1/29)AQP4阳性。在8例MOG抗体阳性患者中,5例有视盘疼痛(p = 0.001),3例有前驱感染(p = 0.179)。8例MOG阳性患者中有3例脑脊液髓鞘碱性蛋白水平显著升高(p = 0.021),脑脊液寡克隆带均为阴性。MRI检查显示,8例MOG阳性患者中有7例视神经呈高信号,3例有脑部病变,1例有脊髓病变。8例MOG阳性患者中有7例对类固醇治疗反应良好。
尽管未证实抗MOG抗体的原发性致病性,但本研究结果表明,检测MOG抗体对视神经炎的诊断和治疗具有重要意义。