医学
髓鞘少突胶质细胞糖蛋白
多发性硬化
荟萃分析
癫痫
免疫学
置信区间
儿科
急性播散性脑脊髓炎
疾病
内科学
精神科
实验性自身免疫性脑脊髓炎
作者
Chun‐Hong Shen,Yang Zheng,Meng‐Ting Cai,Fan Yang,Wei Fang,Yinxi Zhang,Meiping Ding
标识
DOI:10.1016/j.msard.2020.102057
摘要
Abstract
Objective
Recent reports have suggested that seizures may be a component of the clinical presentation in myelin oligodendrocyte glycoprotein antibody (MOG-Ab)-associated disease. We aimed to conduct a systematic review and meta-analysis to comprehensively evaluate the occurrence of epileptic seizures in the disease. Methods
We searched PubMed, MEDLINE and EMBASE for studies reporting the occurrence of acute symptomatic seizures in MOG-Ab-associated disease. Fixed or random effects model was used to pool results across studies with a meta-analysis. Results
A total of 14 studies met the inclusion criteria. Overall, acute symptomatic seizures were observed in 20.5% (95% confidence interval [CI] 13.7%-30.7%, I2=60.6%) patients with MOG-Ab-associated disease, and in a similar proportion of children respectively (20.0%; 95% CI 14.3%-27.8%, I2=7.0%). The pooled probability of seizure occurrence in males was 30.1% (95% CI 17.5%-52%, I2=0.0%) while that in females was much lower (12.0%; 95% CI 5.5%-26.4%, I2=0.0%). Furthermore, when we focused on those with acute disseminated encephalomyelitis-like phenotype, 37.3% patients experienced seizures (95% CI 21.0%-66.3%, I2=55.8%). Conclusions
Our study suggested that epileptic seizures were common in MOG-Ab-associated disease and offered insight into associated factors that contribute to the occurrence of seizures. Future studies with explicit evaluation are required.
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