医学
多发性硬化
视神经脊髓炎
髓鞘少突胶质细胞糖蛋白
发病机制
病理
脑脊液
视神经炎
免疫学
实验性自身免疫性脑脊髓炎
作者
Akiyuki Uzawa,Masahiro Mori,Hiroki Masuda,Mayumi Muto,Ryohei Ohtani,Shinji Aoyama,Kazuyuki Matsushita,Satoshi Kuwabara
标识
DOI:10.1177/13524585241254731
摘要
Background: Myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD) is a rare neuroinflammatory disorder characterized by acute episodes of central nervous system (CNS) demyelination. Previous studies have reported elevated interleukin (IL)-6 in cerebrospinal fluid (CSF) of MOGAD patients. Objective: We examined if CSF IL-6 level increase is associated with clinical parameters in MOGAD. Methods: IL-6 levels were measured using 44 CSF samples during the acute phase and 6 samples during recovery from 34 MOGAD patients, as well as 65 CSF samples from 45 aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder (AQP4Ab + NMOSD), 107 samples from 76 multiple sclerosis patients, and 45 samples from neurodegenerative disease patients. Associations between IL-6 levels and clinical parameters in MOGAD were also evaluated. Results: CSF IL-6 levels were significantly comparably elevated during acute-phase in MOGAD and AQP4Ab + NMOSD, but declined following the acute phase. Among MOGAD patients, CSF IL-6 level was significantly correlated with CSF cell count, greater in patients with brain lesions than spinal cord lesions, and higher in CSF than serum, suggesting that excessive IL-6 is produced predominantly in CNS. Neurological recovery was tended to be poorer in MOGAD patients with higher CSF IL-6 level. Conclusion: CSF IL-6 may play important roles in the pathogenesis of MOGAD, especially in CNS inflammation.
科研通智能强力驱动
Strongly Powered by AbleSci AI