Risk factors of attacks in neuromyelitis optica spectrum disorders

被引:25
|
作者
Akaishi, Tetsuya [1 ,2 ]
Takahashi, Toshiyuki [1 ,3 ]
Fujihara, Kazuo [4 ]
Misu, Tatsuro [1 ]
Abe, Michiaki [2 ]
Ishii, Tadashi [2 ]
Aoki, Masashi [1 ]
Nakashima, Ichiro [5 ]
机构
[1] Tohoku Univ, Dept Neurol, Grad Sch Med, Sendai, Miyagi, Japan
[2] Tohoku Univ Hosp, Dept Educ & Support Reg Med, Sendai, Miyagi, Japan
[3] Natl Hosp Org Yonezawa Natl Hosp, Dept Neurol, Yonezawa, Yamagata, Japan
[4] Fukushima Med Univ, Dept Multiple Sclerosis Therapeut, Fukushima, Japan
[5] Tohoku Med & Pharmaceut Univ, Dept Neurol, Sendai, Miyagi, Japan
关键词
Autoimmune diseases; Infection; Neuromyelitis optica spectrum disorders; Pre-onset history; Surgical operation; AQUAPORIN-4; ANTIBODY; DIAGNOSTIC-CRITERIA; NMO; MARKER; SERUM;
D O I
10.1016/j.jneuroim.2020.577236
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Predisposing factors before the onset of neuromyelitis optica spectrum disorders (NMOSD) have not been systematically evaluated by now. We investigated the detailed pre-onset history in consecutive NMOSD patients. Thirteen of the enrolled 53 NMOSD patients (24.5%) had accompanying autoimmune diseases, such as Sjogren's syndrome. History of malignancy was seen in 8 of the 53 patients (15.1%). Recent history of non-neurological clinical episodes, such as systemic allergic reaction, systemic infection, surgical operation, or traumatic injury, was seen in 23 of the 53 patients (43.4%). NMOSD patients are likely to have pre-onset history of other autoimmune diseases, malignancy, or recent non-neurological systemic conditions, which may predispose or trigger the onset of NMOSD.
引用
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页数:4
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