Trip S Anand, Schlottmann Patricio G, Jones Stephen J, Li Wai-Yung, Garway-Heath David F, Thompson Alan J, Plant Gordon T, Miller David H
NMR Research Unit, Department of Neuroinflammation, Institute of Neurology, University College London, UK.
Neuroimage. 2006 May 15;31(1):286-93. doi: 10.1016/j.neuroimage.2005.11.051. Epub 2006 Jan 27.
Magnetic resonance imaging (MRI) measures of brain atrophy are often considered to be a marker of axonal loss in multiple sclerosis (MS) but evidence is limited. Optic neuritis is a common manifestation of MS and results in optic nerve atrophy. Retinal nerve fibre layer (RNFL) imaging is a non-invasive way of detecting axonal loss following optic neuritis. We hypothesise that if the optic nerve atrophy that develops following optic neuritis is contributed to by axonal loss, it will correlate with thinning of the RNFL. Twenty-five patients were studied at least 1 year after a single unilateral attack of optic neuritis without recurrence, with a selection bias towards incomplete recovery. They had MR quantification of optic nerve cross-sectional area and optic nerve lesion length, as well as optical coherence tomography (OCT) measurement of mean RNFL thickness and macular volume, quantitative visual testing, and visual evoked potentials (VEPs). Fifteen controls were also studied. Significant optic nerve atrophy (mean decrease 30% versus controls), RNFL thinning (mean decrease 33% versus controls), and macular volume loss occurred in patients' affected eyes when compared with patients' unaffected eyes and healthy controls. The optic nerve atrophy was correlated with the RNFL thinning, macular volume loss, visual acuity, visual field mean deviation, and whole field VEP amplitude but not latency. These findings suggest that axonal loss contributes to optic nerve atrophy following a single attack of optic neuritis. By inference, axonal loss due to other post-inflammatory brain lesions is likely to contribute to the global MRI measure of brain atrophy in multiple sclerosis.
磁共振成像(MRI)对脑萎缩的测量通常被认为是多发性硬化症(MS)轴突丢失的一个标志,但证据有限。视神经炎是MS的常见表现,会导致视神经萎缩。视网膜神经纤维层(RNFL)成像是非侵入性检测视神经炎后轴突丢失的方法。我们假设,如果视神经炎后发生的视神经萎缩是由轴突丢失所致,那么它将与RNFL变薄相关。对25例在单次单侧视神经炎发作且无复发至少1年后进行研究的患者进行了研究,这些患者存在偏向不完全恢复的选择偏倚。他们进行了视神经横截面积和视神经病变长度的MR定量分析,以及平均RNFL厚度和黄斑体积的光学相干断层扫描(OCT)测量、定量视觉测试和视觉诱发电位(VEP)检测。还对15名对照者进行了研究。与患者未受影响的眼睛及健康对照者相比,患者受影响眼睛出现了显著的视神经萎缩(平均减少30% 对比对照者)、RNFL变薄(平均减少33% 对比对照者)以及黄斑体积丢失。视神经萎缩与RNFL变薄、黄斑体积丢失、视力、视野平均偏差及全视野VEP波幅相关,但与潜伏期无关。这些发现提示,单次视神经炎发作后轴突丢失导致了视神经萎缩。由此推断,其他炎症后脑病变所致的轴突丢失很可能导致了多发性硬化症中脑萎缩的整体MRI测量结果。