Risk of Guillain-Barre syndrome after COVID-19 vaccination or SARS-CoV-2 infection: A multinational self-controlled case series study

Nasreen, Sharifa and Jiang, Yannan and Lu, Han and Lee, Arier and Cutland, Clare L. and Gentile, Angela and Giglio, Norberto and Macartney, Kristine and Deng, Lucy and Liu, Bette and Sonneveld, Nicole and Bellamy, Karen and Clothier, Hazel J. and Sepulveda Kattan, Gonzalo and Naus, Monika and Naveed, Zaeema and Janjua, Naveed Z. and Nguyen, Lena and Hviid, Anders and Poukka, Eero and Perälä, Jori and Leino, Tuija and Chandra, Lukman Ade and Thobari, Jarir At and Park, Byung-Joo and Choi, Nam-Kyong and Jeong, Na-Young and Madhi, Shabir A. and Villalobos, Felipe and Solórzano, Martín and Bissacco, Carlo Alberto and Carreras-Martínez, Juan Josa and Correcher-Martínez, Elisa and Urchueguía-Fornes, Arantxa and Roy, Debabrata and Yeomans, Alison and Aurelius, Taylor and Morton, Kathryn and Di Mauro, Gianmarco and Sturkenboom, Miriam CJM and Sejvar, James J. and Top, Karina A. and Batty, Karin and Ghebreab, Luam and Griffin, Jennifer B. and Petousis-Harris, Helen and Buttery, Jim and Black, Steven and Kwong, Jeffrey C. (2025) Risk of Guillain-Barre syndrome after COVID-19 vaccination or SARS-CoV-2 infection: A multinational self-controlled case series study. Vaccine, 60: 127291. ISSN 0264410X

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Abstract

Background: The association between Guillain-Barré syndrome (GBS) and certain COVID-19 vaccines is inconclusive. We investigated the risk of GBS after COVID-19 vaccination or SARS-CoV-2 infection. Methods: Using a common protocol, we conducted a self-controlled case series study from 1 December 2020 to 9 August 2023 at 20 global sites within the Global Vaccine Data Network (GVDN). Brighton Collaboration case definition criteria were used to determine the level of certainty (LOC) of medical record-reviewed GBS cases at 15 sites. GBS cases following SARS-CoV-2 infection were identified from electronic data sources (EDS) from 11 sites. We estimated the relative incidence (RI) of GBS within 1-42 days following receipt of adenoviral vector, mRNA, or inactivated COVID-19 vaccines or SARS-CoV-2 infection using conditional Poisson regression models, controlling for seasonality. We used random effects meta-analysis to pool the estimates across sites. Results: Of 410 medical record-reviewed post-vaccination GBS cases (out of 2086 EDS-identified cases), 49 were LOC 1 or 2, 187 were LOC 3 or 4, and 174 were LOC 5. These cases received a total of 794 doses of COVID-19 vaccines (160 20 % adenoviral vector vaccine doses, 556 70 % mRNA vaccine doses, 77 10 % inactivated vaccine doses, and 1 0.1 % protein-based vaccine dose) during the observation period. We observed an increased risk of confirmed (LOC 1-2) GBS after receiving ChAdOx1-S/nCoV-19 (Vaxzevria/Covishield) (RI = 3.10; 95 % confidence interval CI, 1.12-8.62). Decreased risks of LOC 1-4 GBS were observed after receiving BNT162b2 (Comirnaty/Tozinameran) (RI = 0.48; 95 %CI, 0.27-0.85) and CoronaVac/Sinovac (RI = 0.04; 95 %CI, 0.00-0.61). For 489 EDS-identified GBS cases after SARS-CoV-2 infection, we found GBS risk to be increased (RI = 3.35; 95 %CI, 1.83-6.11). Conclusion: In this large multinational study, we found increased risks of GBS within 42 days after Vaxzevria/Covishield vaccination or SARS-CoV-2 infection, and decreased risks after receiving Comirnaty/Tozinameran or CoronaVac/Sinovac COVID-19 vaccines.

Item Type: Article
Additional Information: Cited by: 3; All Open Access; Hybrid Gold Open Access
Uncontrolled Keywords: Adult; Aged; COVID-19; COVID-19 Vaccines; Female; Guillain-Barre Syndrome; Humans; Incidence; Male; Middle Aged; SARS-CoV-2; Vaccination; Vaccines, Inactivated; Young Adult; adenovirus vaccine; coronavac; elasomeran; ibacovavec; SARS-CoV-2 vaccine; tozinameran; vaxzevria; inactivated vaccine; SARS-CoV-2 vaccine; adult; aged; Article; chronic inflammatory demyelinating polyneuropathy; controlled study; coronavirus disease 2019; drug safety; female; Guillain Barre syndrome; health care personnel; hospitalization; human; Human immunodeficiency virus infection; immunocompromised patient; incidence; major clinical study; male; outcome assessment; pharmacovigilance; reverse transcription polymerase chain reaction; risk factor; seasonal variation; self control; sensitivity analysis; Severe acute respiratory syndrome coronavirus 2; sickle cell anemia; stem cell transplantation; vaccination; adverse event; epidemiology; etiology; Guillain Barre syndrome; immunology; middle aged; prevention and control; vaccination; young adult
Subjects: R Medicine > RM Therapeutics. Pharmacology
Divisions: Faculty of Medicine, Public Health and Nursing > Biomedical Sciences
Depositing User: Mukhotib Mukhotib
Date Deposited: 06 Apr 2026 07:50
Last Modified: 06 Apr 2026 07:50
URI: https://ir.lib.ugm.ac.id/id/eprint/26192

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