Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.
Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan.
J Neuroimmunol. 2018 May 15;318:45-52. doi: 10.1016/j.jneuroim.2018.02.002. Epub 2018 Feb 8.
Differential diagnosis for neuromyelitis optica spectrum disorder (NMOSD) and multiple sclerosis (MS) is always doubtful. To differentiate these diseases, we studied the immune status in the blood of patients with MS (n = 45) or NMOSD (n = 23) at remission phase. Remitting NMOSD patients had increased levels of CXCL13 and memory B cells, while remitting MS patients had elevated levels of galectin-9 and Th1 cells. A diagnostic model with these four variables is built to distinguish remitting NMOSD from MS with a sensitivity of 91.30%. Our diagnostic model may help to improve the differentiation of remitting NMOSD from MS.
视神经脊髓炎谱系疾病(NMOSD)和多发性硬化症(MS)的鉴别诊断一直存在疑问。为了区分这些疾病,我们研究了缓解期 MS(n=45)和 NMOSD(n=23)患者血液中的免疫状态。缓解期 NMOSD 患者的 CXCL13 和记忆 B 细胞水平升高,而缓解期 MS 患者的 galectin-9 和 Th1 细胞水平升高。我们建立了一个包含这四个变量的诊断模型,用于区分缓解期 NMOSD 和 MS,其敏感性为 91.30%。我们的诊断模型可能有助于改善缓解期 NMOSD 与 MS 的鉴别诊断。