Zhou Luyao, Liao Ziyu, Long Yingming, Li Zhibin, Qiu Wei, Tan Zefeng, Lu Tingting
Department of Neurology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Department of Radiology, Daping Hospital, Army Medical University, Chongqing, China.
Brain Behav. 2025 Apr;15(4):e70472. doi: 10.1002/brb3.70472.
This study aims to investigate the relationship between treatment delay and poor prognosis in acute myelitis of Neuromyelitis Optica Spectrum Disorder (NMOSD). Additionally, we seek to explore the related factors that contribute to poor prognosis, with the intention of providing more precise clinical guidance.
We retrospectively analyzed the acute myelitis attacks of NMOSD patients who were continuously followed up or referred to our hospital from January 2018 to September 2022. We further calculated the proportion of clinical score improvement: (acute-follow-up)/(acute-baseline); poor prognosis was assigned to 0%-33% improvement. The relationship between treatment delay and poor prognosis was evaluated with clustered Receiver Operating Characteristic (ROC) analysis. A Generalized linear mixed model was used to analyze the related factors.
This study included a total of 144 episodes of myelitis attacks, of which 21.5% (31/144) resulted in poor prognosis. Based on the results of the clustered ROC analysis, it has been determined that treatment delay holds significant predictive value for poor prognosis (p = 0.001), with the optimal cut-off point being 15 days. The generalized linear mixed model revealed that factors contributing to poor prognosis in NMOSD myelitis include age (OR, 1.041; CI, 1.013-1.071; p = 0.004) and treatment delay (OR, 1.034; CI, 1.014-1.054; p = 0.001).
Our results confirm the treatment delay and age as predictors of poor prognosis in acute myelitis of NMOSD.
本研究旨在探讨视神经脊髓炎谱系障碍(NMOSD)急性脊髓炎的治疗延迟与预后不良之间的关系。此外,我们试图探索导致预后不良的相关因素,以便提供更精确的临床指导。
我们回顾性分析了2018年1月至2022年9月期间持续随访或转诊至我院的NMOSD患者的急性脊髓炎发作情况。我们进一步计算了临床评分改善的比例:(急性发作时评分-随访时评分)/(急性发作时评分-基线评分);预后不良定义为改善比例为0%-33%。采用聚类受试者工作特征(ROC)分析评估治疗延迟与预后不良之间的关系。使用广义线性混合模型分析相关因素。
本研究共纳入144例脊髓炎发作病例,其中21.5%(31/144)预后不良。基于聚类ROC分析结果,已确定治疗延迟对预后不良具有显著预测价值(p = 0.001),最佳截断点为15天。广义线性混合模型显示,NMOSD脊髓炎预后不良的因素包括年龄(OR,1.041;CI,1.013 - 1.071;p = 0.004)和治疗延迟(OR,1.034;CI,1.014 - 1.054;p = 0.001)。
我们的结果证实治疗延迟和年龄是NMOSD急性脊髓炎预后不良的预测因素。