Naismith R T, Tutlam N T, Xu J, Klawiter E C, Shepherd J, Trinkaus K, Song S-K, Cross A H
Department of Neurology, Washington University, Box 8111, 660 S. Euclid Ave., St. Louis, MO 63110, USA.
Neurology. 2009 Mar 24;72(12):1077-82. doi: 10.1212/01.wnl.0000345042.53843.d5.
Neuromyelitis optica (NMO) is associated with destructive inflammatory lesions, resulting in necrosis and axonal injury. Disability from multiple sclerosis (MS) is due to a combination of demyelination and varying axonal involvement. Optical coherence tomography (OCT), by measuring retinal nerve fiber layer (RNFL) as a surrogate of axonal injury, has potential to discriminate between these two conditions.
Included were 22 subjects with NMO or NMO spectrum disorders and 47 with MS. Seventeen subjects with NMO and all with MS had a remote history of optic neuritis (ON) in at least one eye, at least 6 months before OCT. Linear mixed modeling was used to compare the two diagnoses for a given level of vision loss, while controlling for age, disease duration, and number of episodes of ON.
After ON, NMO was associated with a thinner mean RNFL compared to MS. This was found when controlling for visual acuity (56.7 vs 66.6 microm, p = 0.01) or for contrast sensitivity (61.2 vs 70.3 microm, p = 0.02). The superior and inferior quadrants were more severely affected in NMO than MS.
Optic neuritis (ON) within neuromyelitis optica (NMO) is associated with a thinner overall average retinal nerve fiber layer compared to multiple sclerosis, with particular involvement of the superior and inferior quadrants. This suggests that NMO is associated with more widespread axonal injury in the affected optic nerves. Optical coherence tomography can help distinguish the etiology of these two causes of ON, and may be useful as a surrogate marker of axonal involvement in demyelinating disease.
视神经脊髓炎(NMO)与破坏性炎性病变相关,可导致坏死和轴突损伤。多发性硬化症(MS)所致残疾是脱髓鞘和不同程度轴突受累共同作用的结果。光学相干断层扫描(OCT)通过测量视网膜神经纤维层(RNFL)作为轴突损伤的替代指标,有可能区分这两种疾病。
纳入22例视神经脊髓炎或视神经脊髓炎谱系障碍患者以及47例多发性硬化症患者。17例视神经脊髓炎患者和所有多发性硬化症患者在进行OCT检查前至少6个月,至少一只眼睛有视神经炎(ON)的既往史。采用线性混合模型,在控制年龄、病程和视神经炎发作次数的同时,比较两种诊断在给定视力丧失水平下的差异。
视神经炎发作后,与多发性硬化症相比,视神经脊髓炎患者的平均视网膜神经纤维层更薄。在控制视力(56.7对66.6微米,p = 0.01)或对比敏感度(61.2对70.3微米,p = 0.02)时均发现这一情况。视神经脊髓炎患者的上象限和下象限比多发性硬化症患者受影响更严重。
与多发性硬化症相比,视神经脊髓炎(NMO)中的视神经炎(ON)与整体平均视网膜神经纤维层更薄相关,尤其以上象限和下象限受累为著。这表明视神经脊髓炎与受累视神经中更广泛存在的轴突损伤有关。光学相干断层扫描有助于区分这两种视神经炎病因,并且可能作为脱髓鞘疾病中轴突受累的替代标志物。