Neurology. 2018 May 22;90(21):e1858-e1869. doi: 10.1212/WNL.0000000000005560. Epub 2018 Apr 25.
To describe clinical and radiologic features associated with myelin oligodendrocyte glycoprotein antibodies (MOG-Ab) in a large French nationwide adult cohort, to assess baseline prognostic features of MOG-Ab-associated diseases after a first acute demyelinating syndrome, and to evaluate the clinical value of MOG-Ab longitudinal analysis.
Clinical data were obtained from 197 MOG-Ab-positive patients ≥18 years of age. Complete imaging data were available in 108, and 54 serum samples were eligible for longitudinal evaluation. For survival analysis comparison, 169 aquaporin-4 antibody (AQP4-Ab)-positive patients from the NOMADMUS database were included.
Median age at onset was 36.46 (range 18.0-76.8) years, and patients were predominantly white (92.9%) with male:female ratio, 1.1. Clinical phenotype at onset included optic neuritis or myelitis in 90.86%, isolated brainstem or encephalopathy syndromes in 6.6%, and a combination of syndromes in 2.5%. Distinctive brain MRI findings in MOG-Ab-positive patients were thalamic and pontine lesions. Cortical and leptomeningeal lesions were found in 16.3% and 6.1%, respectively. The probability of reaching a first relapse after 2 and 5 years was 44.8% and 61.8%, respectively. MOG-Ab-positive patients were at lower risk at presentation of further clinical relapse (hazard ratio [HR] 0.45, 95% confidence interval [CI] 0.26-0.79) compared to AQP4-Ab-positive individuals. MOG-Ab-positive individuals had a lower risk of reaching Disability Status Scale score of 3.0 (HR 0.46, 95% CI 0.22-0.94) and visual acuity of 20/100 (HR 0.23, 95% CI 0.07-0.72). Finally, MOG-Ab titers were higher at relapse than in remission ( = 0.009).
In adults, MOG-Ab-associated disease extends beyond clinical and radiologic abnormalities in the optic nerve and spinal cord. Despite the relapsing course, the overall visual and motor outcome is better compared with AQP4-Ab-positive patients.
描述在法国一个大型全国性成人队列中与髓鞘少突胶质细胞糖蛋白抗体(MOG-Ab)相关的临床和影像学特征,评估首次急性脱髓鞘综合征后 MOG-Ab 相关疾病的基线预后特征,并评估 MOG-Ab 纵向分析的临床价值。
从 197 名年龄≥18 岁的 MOG-Ab 阳性患者中获取临床数据。108 名患者有完整的影像学资料,54 份血清样本符合纵向评估条件。为了进行生存分析比较,纳入了 NOMADMUS 数据库中的 169 名水通道蛋白 4 抗体(AQP4-Ab)阳性患者。
发病时的中位年龄为 36.46 岁(范围 18.0-76.8),患者主要为白人(92.9%),男女比例为 1.1。发病时的临床表型包括视神经炎或脊髓炎 90.86%,孤立性脑干或脑病综合征 6.6%,以及综合征组合 2.5%。MOG-Ab 阳性患者独特的脑部 MRI 表现为丘脑和脑桥病变。皮质和软脑膜病变分别为 16.3%和 6.1%。发病后 2 年和 5 年达到首次复发的概率分别为 44.8%和 61.8%。与 AQP4-Ab 阳性患者相比,MOG-Ab 阳性患者在出现进一步临床复发的风险较低(风险比[HR]0.45,95%置信区间[CI]0.26-0.79)。MOG-Ab 阳性患者达到残疾状态量表评分 3.0(HR0.46,95%CI0.22-0.94)和视力 20/100(HR0.23,95%CI0.07-0.72)的风险较低。最后,MOG-Ab 滴度在复发时高于缓解期( = 0.009)。
在成年人中,MOG-Ab 相关疾病不仅限于视神经和脊髓的临床和影像学异常。尽管存在复发过程,但与 AQP4-Ab 阳性患者相比,总体视觉和运动预后更好。