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

Jeanne Moor, Nicole Toepfner, Wolfgang C. G. von Meissner, Reinhard Berner, Matthias B. Moor, Karolina Kublickiene, Christoph Strumann, Cho-Ming Chao
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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 3-10μg 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 3μg BNT162b2, no sex differences were noted, but after a first dose of 5 or 10μg 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).
德国 5 岁以下儿童接种 BNT162b2 mRNA Covid-19 疫苗(CoVacU5)后症状的性别差异:一项回顾性队列研究
背景许多疫苗不仅在功效上存在性别差异,在不良反应率上也是如此。在此,我们比较了德国 5 岁以下男女儿童在标签外接种 BNT162b2 疫苗的安全性。这是一项回顾性队列研究,我们对通过认证调查收集的数据集进行了事后分析,调查对象是在六家私人诊所和/或两次非专业人员发起的疫苗接种活动中登记接种 SARS-CoV-2 疫苗的 0-<5 岁儿童。我们分析了前 3 剂 3-10μg BNT162b2 的安全性。主要结果是比较接种后 4 种常见症状(如局部症状、全身症状、肌肉骨骼症状和发热)的频率。在双变量分析和回归模型中,根据性别对数据进行了分析,并对年龄、体重和剂量进行了调整。评估了性别与 BNT162b2 剂量之间的交互作用。主动比较分析用于比较 BNT162b2 和非 SARS-CoV-2 疫苗接种后的症状。结果本次分析的数据集包括 7801 名参与者,其中女性 3842 人(占 49%),男性 3977 人(占 51%),年龄为 3 岁(中位数,四分位数之间为 2 岁)。在接受 3μg BNT162b2 治疗的患者中,没有发现性别差异,但在首次接受 5 或 10μg BNT162b2 治疗后,女孩出现局部注射部位症状的比例高于男孩。在逻辑回归中,女性出现局部症状的几率更高,几率比(OR)为 1.33(95% 置信区间 [CI]:1.15-1.55,p<0.05),而全身症状的几率比(OR)为 1.21(95% 置信区间 [CI]:1.01-1.44,p<0.05)。接种非 BNT162b2 儿童疫苗后,女性出现接种后肌肉骨骼症状的几率较低(OR:0.29,95% CI:0.11-0.82,p<0.05)。对接种 BNT162b2 和非 SARS-CoV-2 疫苗进行的主动比较分析表明,女性性别对 BNT162b2 疫苗类型与肌肉骨骼症状之间的关系有积极影响。结论即使是幼儿,接种 BNT162b2 后的症状也存在性别差异。这对审批研究的构想、疫苗接种后的监测以及未来的疫苗接种策略都具有重要意义(德国临床试验注册编号:DRKS00028759)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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