Martinelli V, Comi G, Filippi M, Poggi A, Colombo B, Rodegher M, Scotti G, Triulzi F, Canal N
Department of Neurology, Scientific Institute H.S. Raffaele, University of Milan, Italy.
Acta Neurol Scand. 1991 Sep;84(3):231-6. doi: 10.1111/j.1600-0404.1991.tb04944.x.
Up to now it is still doubtful whether there is a real risk of developing multiple sclerosis (MS) after initial monosymptomatic optic neuritis (ON). In this study we evaluated 43 patients with isolated acute-onset ON, in order to demonstrate the presence of oligoclonal bands (OBs) in the cerebrospinal fluid (CSF) and any additional clinically silent central nervous system (CNS) lesions. All examinations were performed from 5 days to 4 months (mean 43 days), from the onset of visual disturbances. Brain magnetic resonance imaging (MRI) detected white matter areas with increased signal in 21 patients (49%), while somatosensory and brainstem auditory evoked potentials revealed CNS abnormalities in only 5 patients (12%). OBs were present in the CSF of 20 patients (46%). Visual evoked potentials were abnormal in 39 patients (91%). Seven out of the 37 patients (19%) with at least one year follow-up, (mean duration of the follow-up = 32 months, range = 12-74), developed clinically definite MS (CDMS). All 7 patients had positive brain MRI and 6 had positive CSF examination at the basal evaluation. Our data suggest that MRI and CSF-OBs are the most reliable means of identifying patients with isolated ON who subsequently develop CDMS. They may therefore have a predictive value in defining MS risk.
迄今为止,在最初出现单症状性视神经炎(ON)后是否真的存在发生多发性硬化症(MS)的风险仍存疑问。在本研究中,我们评估了43例孤立性急性起病的ON患者,以证明脑脊液(CSF)中寡克隆带(OBs)的存在以及任何其他临床上无症状的中枢神经系统(CNS)病变。所有检查均在视觉障碍发作后的5天至4个月(平均43天)内进行。脑磁共振成像(MRI)在21例患者(49%)中检测到白质区域信号增强,而体感诱发电位和脑干听觉诱发电位仅在5例患者(12%)中显示出CNS异常。20例患者(46%)的CSF中存在OBs。39例患者(91%)的视觉诱发电位异常。在37例至少随访1年的患者中(平均随访时间=32个月,范围=12 - 74个月),有7例(19%)发展为临床确诊的MS(CDMS)。所有7例患者在基础评估时脑MRI均呈阳性,6例CSF检查呈阳性。我们的数据表明,MRI和CSF-OBs是识别随后发展为CDMS的孤立性ON患者的最可靠方法。因此,它们在确定MS风险方面可能具有预测价值。