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评估 CIRCLES 队列中视神经脊髓炎谱系障碍的残疾和疾病负担。

Assessment of disability and disease burden in neuromyelitis optica spectrum disorders in the CIRCLES Cohort.

机构信息

Genentech, Inc, South San Francisco, CA, USA.

Department of Statistics, The Ohio State University, Columbus, OH, USA.

出版信息

Sci Rep. 2024 Oct 30;14(1):26150. doi: 10.1038/s41598-024-75013-z.

DOI:10.1038/s41598-024-75013-z
PMID:39477975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11525583/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bfc/11525583/ca91a1ec5794/41598_2024_75013_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bfc/11525583/5f386bf05f8c/41598_2024_75013_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bfc/11525583/6803e1c45a21/41598_2024_75013_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bfc/11525583/ca91a1ec5794/41598_2024_75013_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bfc/11525583/5f386bf05f8c/41598_2024_75013_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bfc/11525583/6803e1c45a21/41598_2024_75013_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bfc/11525583/ca91a1ec5794/41598_2024_75013_Fig3_HTML.jpg

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本文引用的文献

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