Sex differences in symptoms following the administration of BNT162b2 mRNA COVID-19 vaccine in children below 5 years of age in Germany (CoVacU5): a retrospective cohort study

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Jeanne Moor - , Karolinska Institutet (Author)
  • Nicole Toepfner - , Department of Paediatrics, Medical Faculty Carl Gustav Carus (Author)
  • Wolfgang C G von Meißner - , Universitätsklinikum Schleswig-Holstein - Campus Lübeck (Author)
  • Reinhard Berner - , Department of Paediatrics, Medical Faculty Carl Gustav Carus (Author)
  • Matthias B Moor - , Karolinska Institutet (Author)
  • Karolina Kublickiene - , Karolinska Institutet (Author)
  • Christoph Strumann - , Universitätsklinikum Schleswig-Holstein - Campus Lübeck (Author)
  • Cho-Ming Chao - , Universities of Giessen and Marburg Lung Center (UGMLC), German Center for Lung Research (DZL), Justus Liebig University Giessen (Author)

Abstract

BACKGROUND: Sex differences exist not only in the efficacy but also in adverse event rates of many vaccines. Here we compared the safety of BNT162b2 vaccine administered off-label in female and male children younger than 5 years in Germany.

METHODS: This is a retrospective cohort study, in which we performed a post-hoc analysis of a dataset collected through an authentication-based survey of individuals having registered children aged 0-<5 years for vaccination against SARS-CoV-2 in six private practices and/or two lay person-initiated vaccination campaigns. We analyzed the safety profiles of the first 3 doses of 3-10 µg BNT162b2. Primary outcome was comparison in frequencies of 4 common post-vaccination symptom categories such as local, general, musculoskeletal symptoms and fever. Data were analyzed according to sex in bivariate analyses and regression models adjusting for age, weight, and dosage. Interaction between sex and BNT162b2 dosage was assessed. An active-comparator analysis was applied to compare post-vaccination symptoms after BNT162b2 versus non-SARS-CoV-2 vaccines.

RESULTS: The dataset for the present analysis consisted of 7801 participants including 3842 females (49%) and 3977 males (51%) with an age of 3 years (median, interquartile: 2 years). Among individuals receiving 3 µg BNT162b2, no sex differences were noted, but after a first dose of 5-10 µg BNT162b2, local injection-site symptoms were more prevalent in girls compared to boys. In logistic regression, female sex was associated with higher odds of local symptoms, odds ratio (OR) of 1.33 (95% confidence interval [CI]: 1.15-1.55, p < 0.05) and general symptoms with OR 1.21 (95% CI: 1.01-1.44, p < 0.05). Following non-BNT162b2 childhood vaccinations, female sex was associated with a lower odds of post-vaccination musculoskeletal symptoms (OR: 0.29, 95% CI: 0.11-0.82, p < 0.05). An active comparator analysis between BNT162b2 and non-SARS-CoV-2 vaccinations revealed that female sex positively influenced the association between BNT162b2 vaccine type and musculoskeletal symptoms.

CONCLUSIONS: Sex differences exist in post-vaccination symptoms after BNT162b2 administration even in young children. These are of importance for the conception of approval studies, for post-vaccination monitoring and for future vaccination strategies (German Clinical Trials Register ID: DRKS00028759).

Details

Original languageEnglish
Article number74
Pages (from-to)74
JournalBiology of sex differences
Volume15
Issue number1
Publication statusPublished - 26 Sept 2024
Peer-reviewedYes

External IDs

PubMedCentral PMC11426002
Scopus 85204895660

Keywords

Sustainable Development Goals

ASJC Scopus subject areas

Keywords

  • BNT162b2, COVID-19, Children, SARS-CoV-2, Sex difference, mRNA vaccine