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Enhancing brain lesions during acute optic neuritis and/or longitudinally extensive transverse myelitis may portend a higher relapse rate in neuromyelitis optica spectrum disorders

机译:急性视神经炎和/或纵向广泛性横贯性脊髓炎期间脑部病变的增强可能预示着神经脊髓炎视神经频谱疾病的复发率更高

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摘要

Background and purposeNeuromyelitis optica spectrum disorders (NMOSD) is an inflammatory demyelinating disorder with optic neuritis (ON) and/or longitudinally extensive transverse myelitis (LETM) episodes. We now know that NMOSD is associated with antibodies to aquaporin 4 (AQP4) which is highly concentrated on astrocytic end-feet at the blood-brain barrier. Immune-mediated disruption of blood brain barrier may manifest as contrast enhancement (CE) on brain MRI. We aim to delineate extent and frequency of CE on brain MRI within one month of ON and/or LETM attacks and to correlate CE with outcomes measures.
机译:背景与目的视神经脊髓炎光谱疾病(NMOSD)是一种伴有视神经炎(ON)和/或纵向广泛性横贯性脊髓炎(LETM)发作的炎性脱髓鞘疾病。我们现在知道NMOSD与抗水通道蛋白4(AQP4)的抗体有关,该蛋白高度集中在血脑屏障的星形胶质细胞的末端。免疫介导的血脑屏障破坏可能表现为脑MRI上的对比增强(CE)。我们的目的是描绘ON和/或LETM发作一个月内脑MRI上CE的程度和频率,并将CE与结局指标相关联。

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