Immunological, Clinical, and Epidemiological Features of Guillain-Barré Syndrome Associated with SARS-CoV-2 Infection

IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY Acta Neurologica Scandinavica Pub Date : 2023-02-07 DOI:10.1155/2023/5380946
Juan Luis Restrepo-Vera, A. Llauradó, A. Palasí, V. González-Martínez, M. Gratacós, M. Salvadó, D. Sánchez-Tejerina, J. Sotoca, N. Raguer, R. Juntas-Morales
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引用次数: 3

Abstract

Objectives. There is a growing interest in understanding the association between Guillain-Barré syndrome (GBS) and SARS-CoV-2 infection. The aim of this study was to analyse various characteristics of GBS before and after the pandemic outbreak and thus identify possible distinctive features of GBS associated with SARS-CoV-2 (GBS-S). Material and Methods. In our centre, we retrospectively reviewed the records of patients diagnosed with GBS between January 2018 and March 2022. Epidemiological, clinical, and immunological data were analysed and compared between patients with GBS according to the time of diagnosis and antecedent events. Results. Thirty-nine patients with GBS were included: nine (23.1%) were diagnosed with GBS-S. GBS-S was most frequent in 2020 (6/13, 46.1%). Most of these patients developed a postinfectious classic demyelinating variant (4/9, 44.4%) with frequent bilateral facial paralysis (4/9, 44.4%). Serum antiganglioside antibodies (AGAs) were found in 1/9 patients with GBS-S. Serum anti-SSA/Ro60 antibodies were highly prevalent in GBS-S (7/9 (77.8%) vs. 3/11 (27.3%), p = 0.019 ). Three cases associated with SARS-CoV-2 vaccination (GBS-V) were detected. Of note, two had bilateral facial paralysis and anti-SSA/Ro60 antibodies. Conclusion. Our findings suggest that SARS-CoV-2 has become an important antecedent event associated with GBS in our setting. GBS-S shows a postinfectious demyelinating immune-mediated profile with negative serological testing for AGAs. Serum anti-SSA/Ro60 antibodies were found frequently in these patients. Bilateral facial paralysis stands out as a possible characteristic clinical feature both in GBS-S and GBS-V. Larger, prospective studies are needed for a better understanding of its immunopathogenesis.
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与严重急性呼吸系统综合征冠状病毒2型感染相关的格林-巴利综合征的免疫学、临床和流行病学特征
目标。人们对了解格林-巴利综合征(GBS)与严重急性呼吸系统综合征冠状病毒2型感染之间的关系越来越感兴趣。本研究的目的是分析大流行爆发前后GBS的各种特征,从而确定与严重急性呼吸系统综合征冠状病毒2型(GBS-S)相关的GBS可能的独特特征。材料和方法。在我们的中心,我们回顾性审查了2018年1月至2022年3月期间诊断为GBS的患者的记录。根据诊断时间和先前事件,分析并比较GBS患者的流行病学、临床和免疫学数据。后果包括39例GBS患者:9例(23.1%)被诊断为GBS-S。GBS-S在2020年最为常见(6/13,46.1%)。这些患者中的大多数出现了感染后的经典脱髓鞘变体(4/9,44.4%),并伴有频繁的双侧面瘫(4/9、44.4%)。在1/9的GBS-S患者中发现了血清抗神经节苷脂抗体(AGAs)。血清抗SSA/Ro60抗体在GBS-S中高度流行(7/9(77.8%)对3/11(27.3%),p=0.019)。检测到3例与严重急性呼吸系统综合征冠状病毒2型疫苗接种(GBS-V)相关的病例。值得注意的是,其中两人患有双侧面瘫和抗SSA/Ro60抗体。结论我们的研究结果表明,在我们的环境中,严重急性呼吸系统综合征冠状病毒2型已成为与GBS相关的重要先行事件。GBS-S显示感染后脱髓鞘免疫介导的AGA血清学检测呈阴性。在这些患者中经常发现血清抗SSA/Ro60抗体。双侧面瘫是GBS-S和GBS-V的一个可能的特征性临床特征。需要更大规模的前瞻性研究来更好地了解其免疫发病机制。
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来源期刊
Acta Neurologica Scandinavica
Acta Neurologica Scandinavica 医学-临床神经学
CiteScore
6.70
自引率
2.90%
发文量
161
审稿时长
4-8 weeks
期刊介绍: Acta Neurologica Scandinavica aims to publish manuscripts of a high scientific quality representing original clinical, diagnostic or experimental work in neuroscience. The journal''s scope is to act as an international forum for the dissemination of information advancing the science or practice of this subject area. Papers in English will be welcomed, especially those which bring new knowledge and observations from the application of therapies or techniques in the combating of a broad spectrum of neurological disease and neurodegenerative disorders. Relevant articles on the basic neurosciences will be published where they extend present understanding of such disorders. Priority will be given to review of topical subjects. Papers requiring rapid publication because of their significance and timeliness will be included as ''Clinical commentaries'' not exceeding two printed pages, as will ''Clinical commentaries'' of sufficient general interest. Debate within the speciality is encouraged in the form of ''Letters to the editor''. All submitted manuscripts falling within the overall scope of the journal will be assessed by suitably qualified referees.
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