TY - JOUR
T1 - Autoimmune disorders reported following COVID-19 vaccination
T2 - A disproportionality analysis using the WHO database
AU - Kim, Seohyun
AU - Bea, Sungho
AU - Choe, Seung Ah
AU - Choi, Nam Kyong
AU - Shin, Ju Young
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024.
PY - 2024/3
Y1 - 2024/3
N2 - Purpose: Owing to adverse event following immunization (AEFI) related to autoimmune disorders and coronavirus disease 2019 (COVID-19) vaccines sharing common biological mechanisms, identifying the risk of AEFIs associated with COVID-19 vaccines remains a critical unmet need. We aimed to assess the potential safety signals for 16 AEFIs and explore co-reported adverse events (AEs) and drugs using the global database of the World Health Organization, VigiBase. Methods: We assessed the occurrence of 16 AEFIs following COVID-19 vaccination through the Standardized MedDRA Queries group “Immune-mediated/Autoimmune Disorders” from MedDRA and performed a disproportionality analysis using reporting odds ratio (ROR) and information component (IC) with 95% confidence intervals (CIs). Results: We identified 25,219 events associated with COVID-19 vaccines in VigiBase. Although rare, we detected four potential safety signals related to autoimmune disorders following COVID-19 vaccination, including ankylosing spondylitis or psoriatic arthritis (ROR 1.86; 95% CI 1.53–2.27), inflammatory bowel disease (ROR 1.77; 95% CI 1.60–1.96), polymyalgia rheumatica (ROR 1.42; 95% CI 1.30–1.55), and thyroiditis (ROR 1.40; 95% CI 1.30–1.50), with positive IC025 values. The top co-reported AEs were musculoskeletal disorders, and immunosuppressants were the most representative co-reported drugs. Conclusion: In addressing the imperative to comprehend AEFI related to autoimmune disorders following COVID-19 vaccination, our study identified four potential safety signals. Thus, our research underscores the importance of proactive safety monitoring for the identification of the four AEFIs following COVID-19 vaccination, considering the associated advantages.
AB - Purpose: Owing to adverse event following immunization (AEFI) related to autoimmune disorders and coronavirus disease 2019 (COVID-19) vaccines sharing common biological mechanisms, identifying the risk of AEFIs associated with COVID-19 vaccines remains a critical unmet need. We aimed to assess the potential safety signals for 16 AEFIs and explore co-reported adverse events (AEs) and drugs using the global database of the World Health Organization, VigiBase. Methods: We assessed the occurrence of 16 AEFIs following COVID-19 vaccination through the Standardized MedDRA Queries group “Immune-mediated/Autoimmune Disorders” from MedDRA and performed a disproportionality analysis using reporting odds ratio (ROR) and information component (IC) with 95% confidence intervals (CIs). Results: We identified 25,219 events associated with COVID-19 vaccines in VigiBase. Although rare, we detected four potential safety signals related to autoimmune disorders following COVID-19 vaccination, including ankylosing spondylitis or psoriatic arthritis (ROR 1.86; 95% CI 1.53–2.27), inflammatory bowel disease (ROR 1.77; 95% CI 1.60–1.96), polymyalgia rheumatica (ROR 1.42; 95% CI 1.30–1.55), and thyroiditis (ROR 1.40; 95% CI 1.30–1.50), with positive IC025 values. The top co-reported AEs were musculoskeletal disorders, and immunosuppressants were the most representative co-reported drugs. Conclusion: In addressing the imperative to comprehend AEFI related to autoimmune disorders following COVID-19 vaccination, our study identified four potential safety signals. Thus, our research underscores the importance of proactive safety monitoring for the identification of the four AEFIs following COVID-19 vaccination, considering the associated advantages.
KW - Adverse events
KW - Autoimmune disorders
KW - Coronavirus disease (COVID-19) vaccines
KW - Pharmacovigilance
KW - Reporting odds ratio
UR - https://www.scopus.com/pages/publications/85182170261
U2 - 10.1007/s00228-023-03618-w
DO - 10.1007/s00228-023-03618-w
M3 - Article
C2 - 38212538
AN - SCOPUS:85182170261
SN - 0031-6970
VL - 80
SP - 445
EP - 453
JO - European Journal of Clinical Pharmacology
JF - European Journal of Clinical Pharmacology
IS - 3
ER -