British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada; School of Population and Public Health, University of British Columbia, Vancouver, British Columbia, Canada.
British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada; School of Population and Public Health, University of British Columbia, Vancouver, British Columbia, Canada.
J Am Coll Cardiol. 2022 Nov 15;80(20):1900-1908. doi: 10.1016/j.jacc.2022.08.799.
Postmarketing evaluations have linked myocarditis to COVID-19 mRNA vaccines. However, few population-based analyses have directly compared the safety of the 2 mRNA COVID-19 vaccines.
This study aimed to compare the risk of myocarditis, pericarditis, and myopericarditis between BNT162b2 and mRNA-1273.
We used data from the British Columbia COVID-19 Cohort (BCC19C), a population-based cohort study. The exposure was the second dose of an mRNA vaccine. The outcome was diagnosis of myocarditis, pericarditis, or myopericarditis during a hospitalization or an emergency department visit within 21 days of the second vaccination dose. We performed multivariable logistic regression to assess the association between vaccine product and the outcomes of interest.
The rates of myocarditis and pericarditis per million second doses were higher for mRNA-1273 (n = 31, rate 35.6; 95% CI: 24.1-50.5; and n = 20, rate 22.9; 95% CI: 14.0-35.4, respectively) than BNT162b2 (n = 28, rate 12.6; 95% CI: 8.4-18.2 and n = 21, rate 9.4; 95% CI: 5.8-14.4, respectively). mRNA-1273 vs BNT162b2 had significantly higher odds of myocarditis (adjusted OR [aOR]: 2.78; 95% CI: 1.67-4.62), pericarditis (aOR: 2.42; 95% CI: 1.31-4.46) and myopericarditis (aOR: 2.63; 95% CI: 1.76-3.93). The association between mRNA-1273 and myocarditis was stronger for men (aOR: 3.21; 95% CI: 1.77-5.83) and younger age group (18-39 years; aOR: 5.09; 95% CI: 2.68-9.66).
Myocarditis/pericarditis following mRNA COVID-19 vaccines is rare, but we observed a 2- to 3-fold higher odds among individuals who received mRNA-1273 vs BNT162b2. The rate of myocarditis following mRNA-1273 receipt is highest among younger men (age 18-39 years) and does not seem to be present at older ages. Our findings may have policy implications regarding the choice of vaccine offered.
上市后评估将心肌炎与 COVID-19 mRNA 疫苗联系起来。然而,很少有基于人群的分析直接比较了这 2 种 mRNA COVID-19 疫苗的安全性。
本研究旨在比较 BNT162b2 和 mRNA-1273 疫苗接种后心肌炎、心包炎和心肌心包炎的风险。
我们使用了不列颠哥伦比亚 COVID-19 队列(BCC19C)的数据,这是一项基于人群的队列研究。暴露因素是 mRNA 疫苗的第二剂。结局是在第二剂接种后 21 天内,因心肌炎、心包炎或心肌心包炎在住院或急诊就诊时的诊断。我们使用多变量逻辑回归来评估疫苗产品与感兴趣的结局之间的关联。
mRNA-1273 的每百万第二剂次心肌炎和心包炎发生率高于 BNT162b2(n=31,发生率为 35.6;95%CI:24.1-50.5;n=20,发生率为 22.9;95%CI:14.0-35.4)。mRNA-1273 比 BNT162b2 发生心肌炎的可能性显著更高(调整后的比值比[aOR]:2.78;95%CI:1.67-4.62)、心包炎(aOR:2.42;95%CI:1.31-4.46)和心肌心包炎(aOR:2.63;95%CI:1.76-3.93)。mRNA-1273 与心肌炎的关联在男性(aOR:3.21;95%CI:1.77-5.83)和年轻年龄组(18-39 岁;aOR:5.09;95%CI:2.68-9.66)中更强。
mRNA COVID-19 疫苗接种后心肌炎/心包炎罕见,但我们发现接受 mRNA-1273 疫苗接种的个体中,该风险较 BNT162b2 高出 2-3 倍。mRNA-1273 接种后心肌炎的发生率在年轻男性(年龄 18-39 岁)中最高,而在年龄较大的人群中似乎不存在。我们的发现可能对疫苗接种的选择政策有影响。