Genentech, Inc, South San Francisco, CA, USA.
Department of Statistics, The Ohio State University, Columbus, OH, USA.
Sci Rep. 2024 Oct 30;14(1):26150. doi: 10.1038/s41598-024-75013-z.
Neuromyelitis optica spectrum disorders (NMOSD) comprise autoimmune diseases imposing substantial disability. We compared an NMOSD-targeted disability assessment of mobility, vision, and self-care domains (individually and composite) with the multiple sclerosis-targeted Expanded Disability Status Scale (EDSS) to assess NMOSD disease burden. An overall cohort (n = 505) and a subset of these patients with an enriched dataset (n = 198) were analyzed from the CIRCLES longitudinal, observational database of patients with AQP4-IgG-seropositive or -seronegative NMOSD in North America. Multinomial modeling was used to identify temporal correlates of disability improvement, stability, and worsening. Prior on-study relapse correlated with worsening mobility (OR, 3.08; 95% CI: 1.61-5.90), vision (OR, 3.99; 95% CI: 2.03-7.86), self-care disability (OR, 1.90; 95% CI: 1.07-3.38), and mean composite index disability (OR, 4.20; 95% CI: 1.71-10.34). Higher vision disability was associated with Black race, shorter time on-study, and AQP4-IgG-seropositive status in patients ≥ 18 years (p < 0.05). Disease onset phenotype and sex correlated with pain interference (p < 0.05). These correlates of NMOSD disability were undetected by EDSS. The CIRCLES real-world experience supports the need for NMOSD-specific disability assessment to improve recognition of disease burden, facilitate proactive clinical management, offer insights into resilience, and inform clinical trial design.
视神经脊髓炎谱系疾病(NMOSD)包括自身免疫性疾病,会导致严重残疾。我们比较了 NMOSD 靶向的移动、视力和自我护理领域(单独和综合)的残疾评估与多发性硬化靶向的扩展残疾状况量表(EDSS),以评估 NMOSD 的疾病负担。分析了来自北美 AQP4-IgG 阳性或阴性 NMOSD 患者的 CIRCLES 纵向观察性数据库中的一个总体队列(n=505)和这些患者的一个数据集(n=198)。使用多项建模来确定残疾改善、稳定和恶化的时间相关性。研究前的复发与移动能力恶化(OR,3.08;95%CI:1.61-5.90)、视力恶化(OR,3.99;95%CI:2.03-7.86)、自我护理残疾恶化(OR,1.90;95%CI:1.07-3.38)和平均综合指数残疾恶化(OR,4.20;95%CI:1.71-10.34)相关。更高的视力残疾与黑人种族、研究期间的时间较短以及 18 岁及以上患者的 AQP4-IgG 阳性状态相关(p<0.05)。疾病发作表型和性别与疼痛干扰相关(p<0.05)。EDSS 未检测到 NMOSD 残疾的这些相关性。CIRCLES 的真实世界经验支持需要 NMOSD 特异性残疾评估,以提高对疾病负担的认识,促进主动临床管理,深入了解弹性,并为临床试验设计提供信息。