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中国北方的吉兰-巴雷综合征:对2015年至2020年294例患者的回顾性分析

Guillain-Barré Syndrome in Northern China: A Retrospective Analysis of 294 Patients from 2015 to 2020.

作者信息

Zhai Qiongqiong, Guo Cheng, Xue Fang, Qiang Jing, Li Chaonan, Guo Li

机构信息

Department of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang 050000, China.

Department of Pediatrics, The Third Hospital of Hebei Medical University, Shijiazhuang 050051, China.

出版信息

J Clin Med. 2022 Oct 26;11(21):6323. doi: 10.3390/jcm11216323.

Abstract

Objectives: Acute motor axonal neuropathy (AMAN) was first reported to be the main subtype of Guillain−Barré syndrome (GBS) in northern China in the 1990s. About 30 years has passed, and it is unknown whether the disease spectrum has changed over time in northern China. We aimed to study the epidemiological, clinical, and electrophysiological features of GBS in northern China in recent years. Methods: We retrospectively analyzed the medical records of GBS patients admitted to the Second Hospital of Hebei Medical University in northern China from 2015 to 2020. Results: A total of 294 patients with GBS were enrolled, with median age 53 years and 60.5% of participants being male, and a high incidence in summer and autumn. AMAN was still the predominant subtype in northern China (40.1%). The AMAN patients had shorter time to nadir, longer hospitalization time, and a more severe HFGS score at discharge than acute inflammatory demyelinating polyneuropathies (AIDP) (p < 0.05). With SPSS multivariable logistic regression analysis, we found the GBS disability score (at admission), dysphagia, and dysautonomia were independent risk factors for GBS patients requiring MV (p < 0.05). In comparison with other regions, the proportion of AMAN in northern China (40.1%) was higher than in eastern (35%) and southern (19%) China. Conclusions: AMAN is still the predominant subtype in northern China after 30 years, but there have been changes over time in the GBS spectrum since the 1990s. There are regional differences in GBS in China.

摘要

目的

急性运动轴索性神经病(AMAN)于20世纪90年代首次被报道为中国北方格林-巴利综合征(GBS)的主要亚型。大约30年过去了,中国北方该疾病谱是否随时间发生变化尚不清楚。我们旨在研究近年来中国北方GBS的流行病学、临床和电生理特征。方法:我们回顾性分析了2015年至2020年在中国北方河北医科大学第二医院收治的GBS患者的病历。结果:共纳入294例GBS患者,中位年龄53岁,60.5%的参与者为男性,夏秋发病率高。AMAN仍是中国北方的主要亚型(40.1%)。与急性炎症性脱髓鞘性多发性神经病(AIDP)相比,AMAN患者达到最低点的时间更短,住院时间更长,出院时的高频分级量表(HFGS)评分更严重(p<0.05)。通过SPSS多变量逻辑回归分析,我们发现GBS残疾评分(入院时)、吞咽困难和自主神经功能障碍是GBS患者需要机械通气的独立危险因素(p<0.05)。与其他地区相比,中国北方AMAN的比例(40.1%)高于中国东部(35%)和南部(19%)。结论:30年后,AMAN仍是中国北方的主要亚型,但自20世纪90年代以来GBS谱随时间发生了变化。中国GBS存在地区差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6d9/9658830/b1a512886e6d/jcm-11-06323-g001.jpg

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