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

  • Martina Patone
    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.
  • Xue W. Mei
    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.
  • Lahiru Handunnetthi
    Wellcome Centre for Human Genetics (L.H.), University of Oxford.
  • Sharon Dixon
    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.
  • Francesco Zaccardi
    Leicester Real World Evidence Unit, Diabetes Research Centre (F.Z., K.K.), University of Leicester.
  • Manu Shankar-Hari
    School of Immunology and Microbial Sciences, King's College London, Centre for Inflammation Research (M.S.-H.).
  • Peter Watkinson
    National Institute for Health Research Biomedical Research Centre, Oxford University Hospitals National Health Service Trust (P.W.); University of Oxford.
  • Kamlesh Khunti
    Leicester Real World Evidence Unit, Diabetes Research Centre (F.Z., K.K.), University of Leicester.
  • Anthony Harnden
    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.
  • Carol A.C. Coupland
    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.
  • Keith M. Channon
    British Heart Foundation Centre of Research Excellence, National Institute for Health Research, Oxford Biomedical Research Centre, Radcliffe Department of Medicine, John Radcliffe Hospital (K.M.C.):, University of Oxford.
  • Nicholas L. Mills
    Usher Institute (M.S.-H., N.L.M., A.S.), University of Edinburgh.
  • Aziz Sheikh
    Usher Institute (M.S.-H., N.L.M., A.S.), University of Edinburgh.
  • Julia Hippisley-Cox
    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.

説明

<jats:sec> <jats:title>Background:</jats:title> <jats:p>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.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods:</jats:title> <jats:p>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.</jats:p> </jats:sec> <jats:sec> <jats:title>Results:</jats:title> <jats:p>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]).</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions:</jats:title> <jats:p>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.</jats:p> </jats:sec>

収録刊行物

  • Circulation

    Circulation 146 (10), 743-754, 2022-09-06

    Ovid Technologies (Wolters Kluwer Health)

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