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COVID-19 疫苗序贯接种与 SARS-CoV-2 感染后心肌炎发病风险:按年龄和性别分层。

Risk of Myocarditis After Sequential Doses of COVID-19 Vaccine and SARS-CoV-2 Infection by Age and Sex.

机构信息

Nuffield Department of Primary Health Care Sciences (M.P., X.W.M., S.D., A.H., C.A.C.C., J.H.-C.), University of Oxford.

Wellcome Centre for Human Genetics (L.H.), University of Oxford.

出版信息

Circulation. 2022 Sep 6;146(10):743-754. doi: 10.1161/CIRCULATIONAHA.122.059970. Epub 2022 Aug 22.

Abstract

BACKGROUND

Myocarditis is more common after severe acute respiratory syndrome coronavirus 2 infection than after COVID-19 vaccination, but the risks in younger people and after sequential vaccine doses are less certain.

METHODS

A self-controlled case series study of people ages 13 years or older vaccinated for COVID-19 in England between December 1, 2020, and December 15, 2021, evaluated the association between vaccination and myocarditis, stratified by age and sex. The incidence rate ratio and excess number of hospital admissions or deaths from myocarditis per million people were estimated for the 1 to 28 days after sequential doses of adenovirus (ChAdOx1) or mRNA-based (BNT162b2, mRNA-1273) vaccines, or after a positive SARS-CoV-2 test.

RESULTS

In 42 842 345 people receiving at least 1 dose of vaccine, 21 242 629 received 3 doses, and 5 934 153 had SARS-CoV-2 infection before or after vaccination. Myocarditis occurred in 2861 (0.007%) people, with 617 events 1 to 28 days after vaccination. Risk of myocarditis was increased in the 1 to 28 days after a first dose of ChAdOx1 (incidence rate ratio, 1.33 [95% CI, 1.09-1.62]) and a first, second, and booster dose of BNT162b2 (1.52 [95% CI, 1.24-1.85]; 1.57 [95% CI, 1.28-1.92], and 1.72 [95% CI, 1.33-2.22], respectively) but was lower than the risks after a positive SARS-CoV-2 test before or after vaccination (11.14 [95% CI, 8.64-14.36] and 5.97 [95% CI, 4.54-7.87], respectively). The risk of myocarditis was higher 1 to 28 days after a second dose of mRNA-1273 (11.76 [95% CI, 7.25-19.08]) and persisted after a booster dose (2.64 [95% CI, 1.25-5.58]). Associations were stronger in men younger than 40 years for all vaccines. In men younger than 40 years old, the number of excess myocarditis events per million people was higher after a second dose of mRNA-1273 than after a positive SARS-CoV-2 test (97 [95% CI, 91-99] versus 16 [95% CI, 12-18]). In women younger than 40 years, the number of excess events per million was similar after a second dose of mRNA-1273 and a positive test (7 [95% CI, 1-9] versus 8 [95% CI, 6-8]).

CONCLUSIONS

Overall, the risk of myocarditis is greater after SARS-CoV-2 infection than after COVID-19 vaccination and remains modest after sequential doses including a booster dose of BNT162b2 mRNA vaccine. However, the risk of myocarditis after vaccination is higher in younger men, particularly after a second dose of the mRNA-1273 vaccine.

摘要

背景

严重急性呼吸综合征冠状病毒 2 感染后心肌炎比 COVID-19 疫苗接种后更常见,但在年轻人和序贯疫苗接种后风险不太确定。

方法

对 2020 年 12 月 1 日至 2021 年 12 月 15 日期间在英格兰接种 COVID-19 疫苗的 13 岁及以上人群进行了一项自身对照病例系列研究,按年龄和性别对腺病毒(ChAdOx1)或基于 mRNA 的(BNT162b2、mRNA-1273)疫苗接种后序贯剂量或 SARS-CoV-2 检测阳性后心肌炎的发病风险进行了分层。估计了每百万人接种腺病毒(ChAdOx1)或 mRNA 疫苗后序贯剂量(BNT162b2、mRNA-1273)或 SARS-CoV-2 检测阳性后 1 至 28 天内因心肌炎住院或死亡的超额人数和发病率比值。

结果

在至少接种一剂疫苗的 42842345 人中,21242629 人接种了 3 剂,5934153 人在接种前后感染了 SARS-CoV-2。2861 人(0.007%)发生心肌炎,617 人在接种后 1 至 28 天内发生心肌炎。ChAdOx1 首次接种后 1 至 28 天(发病率比值,1.33[95%CI,1.09-1.62])和 BNT162b2 首次、第二和加强剂量(1.52[95%CI,1.24-1.85];1.57[95%CI,1.28-1.92]和 1.72[95%CI,1.33-2.22])的心肌炎风险增加,但低于接种前后 SARS-CoV-2 检测阳性的风险(11.14[95%CI,8.64-14.36]和 5.97[95%CI,4.54-7.87])。mRNA-1273 第二次接种后 1 至 28 天心肌炎风险较高(11.76[95%CI,7.25-19.08]),加强剂量后仍持续存在(2.64[95%CI,1.25-5.58])。所有疫苗在 40 岁以下男性中的相关性更强。在 40 岁以下男性中,mRNA-1273 第二次接种后的每百万人心肌炎超额事件数高于 SARS-CoV-2 检测阳性(97[95%CI,91-99]与 16[95%CI,12-18])。在 40 岁以下女性中,mRNA-1273 第二次接种和 SARS-CoV-2 检测阳性后的每百万人超额事件数相似(7[95%CI,1-9]与 8[95%CI,6-8])。

结论

总体而言,SARS-CoV-2 感染后心肌炎的风险大于 COVID-19 疫苗接种后,包括 BNT162b2 mRNA 疫苗加强剂量在内的序贯剂量后风险仍然适度。然而,在年轻男性中,尤其是在接受 mRNA-1273 疫苗第二次接种后,疫苗接种后心肌炎的风险更高。

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