Beck Roy W, Trobe Jonathan D, Moke Pamela S, Gal Robin L, Xing Dongyuan, Bhatti M Tariq, Brodsky Michael C, Buckley Edward G, Chrousos Georgia A, Corbett James, Eggenberger Eric, Goodwin James A, Katz Barrett, Kaufman David I, Keltner John L, Kupersmith Mark J, Miller Neil R, Nazarian Sarkis, Orengo-Nania Silvia, Savino Peter J, Shults William T, Smith Craig H, Wall Michael
Optic Neuritis Study Group Coordinating Center, Jaeb Center for Health Research, Tampa, FL 33647, USA.
Arch Ophthalmol. 2003 Jul;121(7):944-9. doi: 10.1001/archopht.121.7.944.
To identify factors associated with a high and low risk of developing multiple sclerosis after an initial episode of optic neuritis.
Three hundred eighty-eight patients who experienced acute optic neuritis between July 1, 1988, and June 30, 1991, were followed up prospectively for the development of multiple sclerosis. Consenting patients were reassessed after 10 to 13 years.
The 10-year risk of multiple sclerosis was 38% (95% confidence interval, 33%-43%). Patients (160) who had 1 or more typical lesions on the baseline magnetic resonance imaging (MRI) scan of the brain had a 56% risk; those with no lesions (191) had a 22% risk (P<.001, log rank test). Among the patients who had no lesions on MRI, male gender and optic disc swelling were associated with a lower risk of multiple sclerosis, as was the presence of the following atypical features for optic neuritis: no light perception vision; absence of pain; and ophthalmoscopic findings of severe optic disc edema, peripapillary hemorrhages, or retinal exudates.
The 10-year risk of multiple sclerosis following an initial episode of acute optic neuritis is significantly higher if there is a single brain MRI lesion; higher numbers of lesions do not appreciably increase that risk. However, even when brain lesions are seen on MRI, more than 40% of the patients will not develop clinical multiple sclerosis after 10 years. In the absence of MRI lesions, certain demographic and clinical features seem to predict a very low likelihood of developing multiple sclerosis. This natural history information is a critical input for estimating a patient's 10-year multiple sclerosis risk and for weighing the benefit of initiating prophylactic treatment at the time of optic neuritis or other initial demyelinating events in the central nervous system.
确定首次视神经炎发作后发生多发性硬化症高风险和低风险相关的因素。
对1988年7月1日至1991年6月30日期间经历急性视神经炎的388例患者进行前瞻性随访,观察多发性硬化症的发生情况。同意参与的患者在10至13年后接受重新评估。
多发性硬化症的10年风险为38%(95%置信区间,33%-43%)。在脑部基线磁共振成像(MRI)扫描中有1个或更多典型病变的患者(160例)风险为56%;无病变的患者(191例)风险为22%(P<0.001,对数秩检验)。在MRI无病变的患者中,男性、视盘肿胀以及存在以下视神经炎非典型特征与较低的多发性硬化症风险相关:无光感视力;无疼痛;以及眼底镜检查发现严重视盘水肿、视乳头周围出血或视网膜渗出。
首次急性视神经炎发作后,如果脑部MRI有单个病变,10年发生多发性硬化症的风险显著更高;病变数量增多并不会明显增加该风险。然而,即使MRI发现脑部病变,超过40%的患者10年后也不会发展为临床多发性硬化症。在无MRI病变的情况下,某些人口统计学和临床特征似乎预示发生多发性硬化症的可能性非常低。这一自然病史信息对于估计患者10年多发性硬化症风险以及权衡在视神经炎或中枢神经系统其他初始脱髓鞘事件时启动预防性治疗的益处至关重要。