Department of Neurology, Mayo Clinic, Rochester, MN 55905, USA.
Neurology. 2010 Dec 7;75(23):2103-9. doi: 10.1212/WNL.0b013e318200d80c.
To asses the presence of cortical demyelination in brains of patients with neuromyelitis optica (NMO). NMO is an autoimmune inflammatory demyelinating disease that specifically targets aquaporin-4-rich regions of the CNS. Since aquaporin-4 is highly expressed in normal cortex, we anticipated that cortical demyelination may occur in NMO.
This is a cross-sectional neuropathologic study performed on archival forebrain and cerebellar tissue sections from 19 autopsied patients with a clinically and/or pathologically confirmed NMO spectrum disorder.
Detailed immunohistochemical analyses of 19 archival NMO cases revealed preservation of aquaporin-4 in a normal distribution within cerebral and cerebellar cortices, and no evidence of cortical demyelination.
This study provides a plausible explanation for the absence of a secondary progressive clinical course in NMO and shows that cognitive and cortical neuroimaging abnormalities previously reported in NMO cannot be attributed to cortical demyelination. Lack of cortical demyelination is another characteristic that further distinguishes NMO from MS.
评估视神经脊髓炎(NMO)患者脑内是否存在皮质脱髓鞘。NMO 是一种自身免疫性炎症性脱髓鞘疾病,专门针对中枢神经系统中富含水通道蛋白-4 的区域。由于水通道蛋白-4 在正常皮质中高度表达,我们预计 NMO 中可能会发生皮质脱髓鞘。
这是一项在 19 例经临床和/或病理证实的 NMO 谱障碍尸检患者的存档前脑和小脑组织切片上进行的横断面神经病理学研究。
对 19 例存档的 NMO 病例进行详细的免疫组织化学分析显示,水通道蛋白-4 在大脑和小脑皮质内呈正常分布,无皮质脱髓鞘证据。
本研究为 NMO 中无继发性进行性临床病程提供了合理的解释,并表明以前在 NMO 中报道的认知和皮质神经影像学异常不能归因于皮质脱髓鞘。缺乏皮质脱髓鞘是 NMO 与 MS 进一步区分的另一个特征。