Zhang Meini, Zhang Chuntao, Bai Peng, Xue Huiru, Wang Guilian
Department of Neurology, First Hospital of Shanxi Medical University, No. 85 Jiefangnan Road, Taiyuan, 030001, Shanxi, China.
Acta Neurol Belg. 2017 Sep;117(3):695-702. doi: 10.1007/s13760-017-0795-6. Epub 2017 Jun 12.
Neuromyelitis optical (NMO) and neuromyelitis optical spectrum disorder (NMOSD) are inflammatory autoimmune demyelination diseases affecting the central nervous system. We investigated the efficiency of low-dose rituximab treatment in 31 Chinese patients with NMO/NMOSD across a median period of 2.29 ± 0.97 years and azathioprine combined with corticosteroid treatment in 34 Chinese patients with NMO/NMOSD across a median period of 2.61 ± 0.94 years. Among the rituximab-treated patients, the mean Expanded Disability Status Scale (EDSS) was 5.62 ± 1.35 before treatment and 4.48 ± 0.78 at last follow-up, and the mean annualized relapse rate (ARR) was 1.39 ± 0.42 before treatment and 0.03 ± 0.13 at last follow-up. Among the azathioprine-treated patients, the mean EDSS was 5.63 ± 1.29 before treatment and 5.05 ± 1.00 at last follow-up, and the mean ARR was 1.28 ± 0.34 before treatment and 0.49 ± 0.21 at last follow-up. In this study, we showed that using low-dosage rituximab could benefit Chinese patients with NMO by reducing the new occurrence of relapses dramatically. Compared with the azathioprine-treated patients, we concluded that rituximab is more effective in preventing NMO relapse and could improve the symptoms.
视神经脊髓炎(NMO)和视神经脊髓炎谱系障碍(NMOSD)是影响中枢神经系统的炎症性自身免疫性脱髓鞘疾病。我们对31例中国NMO/NMOSD患者进行了中位时间为2.29±0.97年的低剂量利妥昔单抗治疗效果研究,并对34例中国NMO/NMOSD患者进行了中位时间为2.61±0.94年的硫唑嘌呤联合皮质类固醇治疗。在接受利妥昔单抗治疗的患者中,治疗前平均扩展残疾状态量表(EDSS)评分为5.62±1.35,末次随访时为4.48±0.78,治疗前平均年化复发率(ARR)为1.39±0.42,末次随访时为0.03±0.13。在接受硫唑嘌呤治疗的患者中,治疗前平均EDSS评分为5.63±1.29,末次随访时为5.05±1.00,治疗前平均ARR为1.28±0.34,末次随访时为0.49±0.21。在本研究中,我们表明使用低剂量利妥昔单抗可通过显著减少新的复发事件使中国NMO患者获益。与接受硫唑嘌呤治疗的患者相比,我们得出结论,利妥昔单抗在预防NMO复发方面更有效,且能改善症状。