CASE REPORT article

Front. Cardiovasc. Med., 27 April 2022

Sec. General Cardiovascular Medicine

Volume 9 - 2022 | https://doi.org/10.3389/fcvm.2022.844626

Case Report: Importance of MRI Examination in the Diagnosis and Evaluation of COVID-19 mRNA Vaccination Induced Myocarditis: Our Experience and Literature Review

  • 1. Department of Cardiology, Japanese Red Cross Musashino Hospital, Tokyo, Japan

  • 2. Department of Cardiology, Tokyo Medical and Dental University, Tokyo, Japan

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Abstract

Acute myocarditis is a rare but serious complication associated with mRNA-based coronavirus disease 2019 (COVID-19) vaccination. In this article, four COVID-19 mRNA vaccination induced myocarditis cases managed at our tertiary Medical Center have been discussed. Three patients had typical myocarditis. One patient suffered from atrioventricular block and heart failure, which required more intensive treatment, but eventually improved. Additionally, a review of cardiac magnetic resonance imaging (MRI) features related to the diagnosis of myocarditis showed that COVID-19 mRNA vaccine-associated myocarditis tend to have more late-gadolinium enhancement (LGE) accumulation in the inferior lateral wall direction. According to a report by the U.S. Centers for Disease Control and Prevention (CDC), the diagnosis of COVID-19 mRNA vaccine-associated myocarditis is based on clinical symptoms, altered myocardial enzymes, cardiac MRI finding, or histopathology. Cardiac MRI is relatively less invasive than myocardial biopsy and plays an important role in the diagnosis of myocarditis. This review may aid in the diagnosis of COVID-19 mRNA vaccine-associated myocarditis.

Introduction

The Ministry of Health, Labor and Welfare Japan approved a range of coronavirus disease 2019 (COVID-19) vaccines in February 2021, and vaccination has been since then widely promoted by the government through various health education campaigns and initiatives. By the end of November 2021, 79.2% of the Japanese population had received their first dose of the COVID-19 vaccine, and 77.3% had received their second dose (1).

As the younger population started receiving vaccines, adverse events different from those commonly seen in older adults began to occur, including myocarditis. In general, myopericarditis is a very rare adverse event associated with vaccination and has been reported particularly after administration of the smallpox vaccine (2, 3). To the best of our knowledge, in the case of COVID-19, as this is the first time that mRNA vaccines have been used clinically, the current occurrence of post-vaccination myocarditis is of particular concern.

In this study, several cases of myocarditis that were suspected to be associated with mRNA-based COVID-19 vaccination were reviewed, and a literature review has been presented regarding the efficacy and utility of late-gadolinium enhancement (LGE) on cardiac magnetic resonance imaging (cMRI) in the diagnosis of myocarditis.

Case Presentation

From February to October 2021, four patients with COVID-19 mRNA vaccine-associated myocarditis were admitted to our hospital (Table 1). The diagnosis was based on the definition reported by the U.S. Centers for Disease Control and Prevention (CDC) (4). All patients fulfilled the Lake Louise Criteria (LLC) (5), which is considered as a diagnostic criterion for myocarditis on cMRI.

Table 1

Case 1Case 2Case 3Case 4
DefinitionConfirmedConfirmedConfirmedConfirmed
Age, y19202948
SexMaleMaleMaleMale
Race/ethnicityCaucasianAgainAgainAgain
Vaccine type
Types of mRNA vaccinesmRNA-1273-ModernamRNA-1273-ModernamRNA-1273-ModernaBNT162b2 mRNA-Pfizer-BioNTech
Number of vaccinations2221
History of previous COVID-19 infectionDenied/ negative antigenDenied/ negative antigenDenied/ negative PCRDenied/ negative PCR
Symptoms
Day 1 post-vaccinationChest discomfortFeverFeverNo symptom
Day 2 post-vaccinationChest pain, pain with breathing, hospital admissionChest pressure, nauseaChest pain, hospital admissionFever, tiredness, diarrhea
Day 3 post-vaccinationHospital admissionTiredness
Day 4 post-vaccinationTiredness
Day 5 post-vaccinationSyncope, tiredness, hospital admission
Vital signs at presentation
Temperature, °C36.939.136.235.4
Heart rate, bpm1001067380
Blood pressure, mm Hg109/58120/57117/6985/57
Respirations, per min18201820
Chest x-ray findingsNo acute pulmonary diseaseNo acute pulmonary diseaseNo acute pulmonary diseaseenlarged cardiac shadow
Cardiothoracic ratio (CTR)48.4%48.4%43.4%54.5%
ECG findings
ST changesNoST elevation in V3–6NoNegative T wave in V4–6
RhythmNormal sinus rhythmNormal sinus rhythmNormal sinus rhythmParoxysmal atrioventricular block
Echocardiogram
Number of days after vaccination3 days5 days3 days5 days
LV ejection fraction52625830
LV end-diastolic internal dimension48514047
LV end-systolic internal dimension35362836
Intraventricular septal diastolic thickness910914
LV posterior wall thickness12101215
E/A2.091.71.130.63
E/e'3.687.154.659.02
Regional wall motion abnor- malitiesNoneNoneNonDiffuse hypokinesis
Diastolic functionNormalNormalNormal
Cardiac magnetic resonance imaging (cMRI)
Number of days between last vaccination and cMRI5 days6 days (first time)45 days (second time)12 days12 days
LGESub-epicardial wall of basal-mid infero-lateral LVNamid wall of basal inferior LVmid wall of anterior, and inferior LVMid-wall of basal inferior, Sub-epicardial wall of mid- and infero-septum LV
DefinitionConfirmedConfirmedConfirmedConfirmed
T2WBB high signalSub-epicardial wall of basal-mid infero-lateral LVmid wall of basal inferior LVNamid wall of anterior, and inferior LVMid-wall of basal inferior, Sub-epicardial wall of mid- and infero-septum LV
Laboratory findings
Cardiac troponin I pg/mL
Presentation1,801.71,885.64,419.617,888.7
Peak5,321.95,7494,419.617,888.7
Postdischarge<10 <10<1015.5
CK U/L peak415324154765
CK-MB U/L peak30.815.3964
WBC6,5005,9006,1005,000
BNP, pg/mL9.112.19111
CRP, mg/dL5.638.781.1611.32
Coronary angiography findingsNDMRI negativeCCT negativeCAG no stenosis
Clinical course
Hospitalization duration58511
Treatment(s)Ibuprofen, ACE-IIbuprofen, ACE-IIbuprofen, ACE-Idobutamine, Diuretic, Ibuprofen, ACE-I

Patient demographic and medicals characteristics and associated health outcomes.

BNP, B-type natriuretic peptide; COVID-19, coronavirus disease 2019; CRP, C-reactive protein; E/A, transmitral Doppler early (E-wave) to late (A-wave) ventricular filling velocities; E/e', E-wave to tissue Doppler early diastolic mitral annular velocity; LGE, late gadolinium enhancement; LV, left ventricular; T2WBB, T2 Weighed black blood; WBC, white blood cell.

The study was approved by the institutional review board of the Japanese Red Cross Musashino Hospital and was conducted in accordance with the ethical principles of the Declaration of Helsinki as well as with the Japanese Ethical Guidelines for Medical and Health Research Involving Human Subjects. All participants provided their written informed consent for the anonymized publication of these findings and were provided information disclosure documents on our website. The participants were free to opt out of participation at any time without any adverse consequences or the loss of benefits to which they were otherwise entitled.

Case 1, Case 2, and Case 3

These three cases are relatively similar. Male patients under 30 years of age had developed myocarditis after their second dose of vaccination. They experienced some kind of chest symptoms such as chest pain and chest pressure within a few days after vaccine administration. Electrocardiography changes (ST elevation) were observed only in Case2. Particularly, negative T waves appeared after ST elevation; these negative T waves improved over time. High-sensitivity troponin-I levels were elevated in all cases, and creatine kinase-myocardial band (CK-MB) was also elevated to above the reference level in Case 1 and Case 2. There was no elevation of white blood cell (WBC) and B-type natriuretic peptide (BNP), but C-reactive protein (CRP) levels were elevated in all patients. Cardiac MRI was performed in all patients. LGE was observed in each case with varying localization, and was more common in the sub-epicardial wall. In Cases 1 and Case 3, T2 high signal intensity and LGE were observed simultaneously in the same segment. In Case 2, an examination performed 6 days after vaccination showed only T2 high signal intensity at the sub-epicardial wall of the basal inferior left ventricle. However, an examination performed 47 days later showed LGE in the same area and likewise demonstrated that the T2 high signal intensity had disappeared. Ibuprofen was administered to all patients due to its anti-inflammatory effects. An angiotensin-converting enzyme inhibitor (ACE-I) was administered as well to prevent remodeling.

Case 4

Case 4 had a relatively different course compared to the previous three cases. The patient developed fever the day after first dose vaccination, and was referred to the hospital 5 days after vaccination with syncope as the chief complaint. An electrocardiogram revealed paroxysmal atrioventricular block, which was thought to be the cause of syncope. Although a pacemaker lead had to be temporarily inserted for AV block, the paroxysmal AV block resolved 2 days after admission. On echocardiography, marked myocardial hypertrophy and decreased left ventricular contractility were observed. Improvements in hypertrophy and contraction were observed on subsequent echocardiography. In laboratory findings, compared to the previous three cases, BNP levels were elevated, and high-sensitivity troponin-I and CK-MB levels were relatively high. On cardiac MRI, T2 high signal intensity and LGE were observed simultaneously in the mid-wall of basal inferior and sub-epicardial wall of mid-septum and infero-septum left ventricular. Only this patient had an accumulation of LGE and high T2 signal on the left ventricular septum side (Figure 1). Catecholamines (i.e., dobutamine) and diuretics were administered during hospitalization as a treatment for heart failure. Diuretic, ibuprofen, and ACE-I were discontinued following confirmation of negative troponin levels in the outpatient clinic, with no apparent adverse events.

Figure 1

Figure 1

Cardiac magnetic resonance imaging (MRI) of all profiled cases. Case 1: T2 high signal intensity and late-gadolinium enhancement (LGE) were observed at the sub-epicardial wall of the basal-mid inferolateral left ventricular (LV). Case 2: T2 high signal intensity and LGE were observed at the mid wall of the basal inferior LV. Case 3: T2 high signal intensity and LGE were observed at the mid wall of the anterior, and at the inferior LV. Case 4: T2 high signal intensity and LGE were observed at the mid-wall of basal inferior, and at the sub-epicardial wall of the mid- and inferoseptum LV.

Discussion

COVID-19 mRNA Vaccination-Associated Myocarditis

The CDC has recently reported diagnostic criteria for post-vaccination myocarditis (4). The criteria for diagnosis include specific clinical symptoms following vaccination, as well as cMRI findings consistent with myocarditis in the presence of troponin levels above the upper limit of normal and/or histopathologic confirmation of myocarditis. The diagnosis of myocarditis on cMRI is based on the implementation of either the original or the revised LLC (5, 6). We note that cMRI is less invasive than myocardial biopsy and is considered an important diagnostic tool for evaluating vaccine-associated myocarditis.

In this case series, cMRI was performed in all the cases. In Cases 1, 3, and 4, T2 high signals and LGE were observed simultaneously in the same segment, which was considered to fulfill the LLC. In Case 2, T2 high signal intensity was seen on initial examination. Later examination demonstrated the appearance of LGE in the same region. The initial examination showed inflammatory findings, and the LGE observed on the second examination was thought to be the result of fibrosis occurring due to these inflammatory findings. During the observation period, there were cases in which the MRI showed only LGE and no T2 findings, so the LLC could not be fulfilled, and the diagnosis could not be confirmed. More specifically, though these cases had clinical presentations consistent with myocarditis, there are two reasons they were not classified as confirmed cases. First, the quality of MRI was a limiting factor. Namely, the quality of cMRI at our hospital was unacceptable; specifically, the myocardial early gadolinium enhancement ratio could not be evaluated and used parametric mapping techniques with the currently available technology. Thus, findings of sufficient quality might not have been obtained; and may thus, have failed to confirm true myocarditis cases. The second limiting factor is the accuracy of the LLC. Though the LLC present a widely used diagnostic classification system for myocarditis, previous studies have reported that the sensitivity of diagnosing myocarditis when two out of the three main criteria were fulfilled was only ~78% (7). Thus, the accuracy of these criteria alone may not be sufficient to accurately diagnose myocarditis with acceptable sensitivity and specificity. However, studies to date indicate that the modified version of the LLC may provide more accuracy if parametric mapping techniques can be applied (6).

Cardiac MRI for Myocarditis

Numerous cases of COVID-19 mRNA vaccine-associated myocarditis have been reported till date. cMRI plays an important role in the diagnosis of any form of myocarditis. The American Heart Association (AHA) scientific statement on the management of myocarditis (8) as well as the current European Society of Cardiology (ESC) position statement (9) consider cMRI useful for the evaluation of suspected myocarditis. Japanese guidelines likewise suggest its usefulness (10). More specifically, cMRI provides a non-invasive, biopsy-like approach in order to verify the pathognomonic imaging features associated with and plays a role in the exclusion of myocardial inflammation. The current ESC guidelines on acute and chronic heart failure include a Class I indication for the efficacy of cMRI in the assessment of myocarditis (11). cMRI characteristics of myocardial inflammation may not only aid in the diagnosis of myocarditis but may also provide important and accurate information on prognoses. In acute cases, myocardial edema presenting without LGE on cMRI has been associated with improved recovery and outcomes (12). The relationship between the localization of LGE on cMRI and mortality in myocarditis has been reported as well (13). Thus, cMRI has evolved to become a key evaluation tool in patients with suspected myocardial inflammation.

Significance of LGE in Myocarditis

LGE is not an essential finding in the original or revised LLC for the diagnosis of myocarditis. However, LGE is the most established technique for detecting myocardial damage (14). The presence of LGE seems to be a good predictor of adverse outcomes in patients with biopsy-proven myocarditis, and has been shown to be superior to other variables in this regard (15). Some recent reports suggest that the location, pattern, extent, and distribution of LGE can stratify the risk for patients with suspected myocarditis. For example, Gräni et al. reported that septal and mid-wall LGE were most strongly associated with major cardiovascular events, including all-cause mortality, worsening heart failure, heart transplantation, and ventricular arrhythmias (16). Aquaro et al. showed that patients with anteroseptal LGE have a worse prognosis than those with LGE at other sites (17). Greulich et al. demonstrated that the presence of mid-wall LGE in the septal segments was associated with a higher long-term mortality rate as compared with the absence of LGE or other LGE patterns in patients with biopsy-proven viral myocarditis (13). One reported mechanism potentially mediating these effects is that the septal LGE might involve the conduction system, thus yielding the substrate for malignant arrhythmias (13). Among the cases presented in this report, only Case 4 revealed LGE in the septal segment. Specifically, Case 4 showed paroxysmal atrioventricular block as a disturbance of the conduction system; this case presentation was relatively severe as compared to the other three cases and thus necessitated intensive treatment. The importance of attaining a greater comprehension of LGE characteristics on cMRI of patients with myocarditis has been emphasized.

LGE in COVID-19 mRNA Vaccination-Associated Myocarditis

There have been numerous reports of COVID-19 mRNA vaccination-associated myocarditis in recent months; however, adverse reactions are relatively rare and comprehensive reports are limited. Shiyovich et al. reported 15 cases of vaccine-associated myocarditis; and, to the best of our knowledge, it is the largest case series published till date (18). In that report, LGE was observed in 13/15 patients with vaccine-associated myocarditis, and was more common in the inferolateral region.

“PubMed” was mainly accessed and reports were extracted using the keywords “myocarditis,” “mRNA vaccination,” and “COVID-19.” Cases, articles, and review articles without detailed MRI descriptions were excluded. Finally, numerous cases of COVID-19 mRNA vaccination-associated myocarditis presented within 24 publications were reviewed, all of which described the localization of LGE. A total of 62 cases (four cases evaluated by the study authors in the current report, and 58 cases evaluated within previously published case reports and case series) were reviewed in terms of diagnostic imaging, with a focus on LGE findings of cMRI (1841). The localization was classified as anterior, anterolateral, lateral, inferolateral, inferior, inferoseptal, mid-septal, and anteroseptal. The layers of the myocardium were classified as epicardial or sub-epicardial, mid, and endocardial or sub-endocardial wall. Vertical localization (basal, mid, apical) was not described in many of the cases (i.e., only transverse localization was evaluated). In the present review, the examined cases comprised 61 males and one female with an average age of 29 (±12.4) years. Forty-one patients (66.1%) were under the age of 30 years. Forty-six patients (74.2%) had been vaccinated with the Pfizer mRNA-based vaccine and 16 patients (25.8%) had been vaccinated with Moderna mRNA-based vaccine. Table 2 and Figure 2 summarize the LGE features within cMRI. We found that LGE occurred more frequently on the free wall side (i.e., mainly in the inferolateral region) and occurred relatively less frequently on the septal side. LGE was mostly detected on the epicardia or sub-epicardia; no case with LGE on the left ventricular endocardia was identified.

Table 2

AgeSexVaccine typesNumber of vaccinationsTime from last vaccination to cardiac MRILGE: layerLGE: segment
Marshall et al.Case 116MalePfizer2ndNASubepicardiaApical and midchamber lateral wall
Case 219MalePfizer2ndNAMid wallBasal inferolateral wall
Case 317MalePfizer2ndNASubepicardialBasal anterolateral segment, basal to midventricular inferolateral segments
Case 517MalePfizer2ndNAEpicardiaAnterior and lateral LV
Case 714MalePfizer2nd5 daysSubepicardialMid and apical left ventricle free wall
Rosner et al.Case 239MalePfizer2nd11 daysSubepicardialAlong the anterior and lateral walls
Case 339MaleModelna2nd5 daysSubepicardial and midmyocardialAnterior wall
Case 424MalePfizer1st7 daysMidmyocardialSeptal and inferior walls
MaleSubepicardialAnterior, lateral, and inferior walls
Case 519MalePfizer2nd3 daysMultifocal patchy subepicardial and midmyocardialLateral and inferolateral walls
Case 620MalePfizer2nd6 daysSubepicardialLateral, inferolateral, anterolateral walls, apex
Case 723MalePfizer2nd3 daysMid wallBasal anteroseptal
Mouch et al.Case 124MalePfizer2ndNASubepicardialBasal septum
Mid myocardialInferolateral
Case 220MalePfizer2ndNASubepicardialBasal and middle anterolateral and inferolateral walls
Case 329MalePfizer2ndNADiffuseBasal, inferolateral, anterolateral and anteroseptal walls
Case 445MalePfizer1stNASubepicardialMiddle anterolateral, inferolateral and apical anterior walls
Case 516MalePfizer2ndNAMidmyocardialBasal inferolateral
MaleSubepicardialMiddle anterolateral
Case 617MalePfizer2ndNASubepicardialBasal inferolateral, middle inferolateral and infero-septal and apical lateral, anterior and inferior walls
Mid-myocardialMiddle inferolateral and anterolateral and apical anterior and lateral walls
Kim et al.Case 136MaleModerna2nd3 daysEpicardialApical lateral
Case 424MalePfizer2nd3 daysEpicardial, patchyLateral
Ammirati et al.56MalePfizer2ndNASubepicardial-intramyocardial regionsBasal and apical segments of the infero-lateral wall
Angelo et al.30MalePfizer2nd6 daysSubepicardialSparing of the basal and mid-septal segments
Albert et al.24MaleModerna2nd5 daysMid-myocardial and epicardialLateral, anterolateral and inferolateral segments
Muthukumar et al.52MaleModerna2nd6 daysMidmyocardial and subepicardialInfero-septal, inferolateral, anterolateral, and apical walls
SubepicardialInferior basal and mesocardial midventricular region
Minocha et al.17MalePfizer2ndNASubepicardialMid-lateral and apical
Mansour et al.Case 125MaleModerna2nd6 daysSubepicardialAnterolateral wall of the mid and apical left ventricle
Case 221FemaleModerna2nd4 daysSubepicardialInferolateral wall at the base
Habib et al.37MalePfizer2ndNASubepicardialBasal lateral wall
Cereda et al.21MalePfizer2ndNAPatchy epicardialThe posterior, anterior, inferior, and lateral walls
Vidula et al.Case 119MalePfizer2ndNASubepicardialBasal to mid lateral wall
Case 218MaleModerna2ndNASubepicardialMid lateral wall
Williams et al.34MaleModerna2nd7 daysSubepicardialAnterolateral and inferolateral segments
Isaak et al.15MalePfizer2ndNASubepicardialInferolateral wall
Hasnie et al.22MaleModerna1stNASubepicardialLateral wall and inferior segments at the midventricular and apical LV
Patrignani et al.56MalePfizer1st11 daysSub-epicardialBasal and middle segments of the infero-lateral wall
Kim et al.24MalePfizer2ndNASub-epicardialBasal inferior and inferolateral segment
Ehrlich et al.40MalePfizer1st12 daysDiffuseBasal and mid anteroseptal and inferoseptal segments as well as in the apical septal segment
Patel et al.Case 122MalePfizer1stNASubepicardialBasal inferior, basal inferolateral, and apical lateral
Case 219MalePfizer2ndNASubepicardialBasal inferolateral
Case 325MaleModerna2ndNASubepicardialLateral
Case 437MalePfizer2ndNASubepicardialBasal anteroseptal segment
Case 520MalePfizer2ndNASubepicardial and mid-myocardialBasal, mid, and apical lateral segments
Tailor et al.44MaleModerna2nd5 daysMid-myocardialMid-septum, infero-septum, and inferior walls at the base to midventricle
Sub-epicardial and mid-myocardialLateral wall at the mid-ventricle and apical lateral wall
Nguyen et al.20MaleModerna1stNASubepicardialMid and basal inferolateral segments
Onderko et al.Case 228MalePfizer2ndNAEpicardiumApical lateral wall, midanterolateral segments
Case 336MaleModerna2ndNAEpicardialMid- to distal inferolateral and lateral walls
Shiyovich et al.Case 141MalePfizer2nd107 daysMid-wallInferolateral (basal)
Case 224MalePfizer2nd103 daysMid-wall and epicardiaInferolateral (basal)
Case 317MalePfizer2nd7 daysEpicardialInferolateral, anterolateral, (basal to apical)
Case 437MalePfizer1st48 daysEpicardialInferolateral (basal, mid)
Case 539MalePfizer2nd8 daysMid-wall and epicardiaInferoseptal, anteroseptal (basal), inferolateral, anterolateral (basal), Inferolateral (med), septum, lateral (apical)
Case 719MalePfizer2nd43 daysMid-wallInferior (apicalbasal), Inferolateral (mid, basal), anterior (basal, mid), septum, lateral (apical)
Case 828MalePfizer2nd139 daysMid-wallInferolateral, anterolateral (basal)
Case 1017MalePfizer2nd17 daysEpicardialInferior, inferolateral (basal), inferior, inferoseptal, inferolateral (mid)
Case 1136MalePfizer1st63 daysMid-wallLateral (apical)
Case 1227MalePfizer2nd105 daysEpicardialInferolateral (basal)
Case 1342MalePfizer1st53 daysEpicardialInferolateral (apical, basal), anterolateral (basal)
Case 1476MalePfizer2nd117 daysMid-wallInferolateral (basal)
Case 1532MalePfizer2nd83 daysMid-wallInferior (basal), inferolateral (basal)
Our CasesCase 119MaleModerna2nd5 daysSub-epicardialInfero-lateral (basal-mid)
Case 220MaleModerna2nd45 daysMid-wallInferior (basal)
Case 329MaleModerna2nd12 daysmid-wallAnterior, inferior wall
Case 448MalePfizer1st12 daysMid-wallInferior walls at the base to midventricle
SubepicardialMid-septum, and infero-septum of left ventricular Wall

Published case reports and case series regarding COVID-19 vaccine-associated myocarditis that describe LGE on cardiac magnetic resonance imaging (MRI).

LGE, late-gadolinium enhancement; LV, left ventricular.

Figure 2

Figure 2

A summary of results regarding late-gadolinium enhancement (LGE) on cardiac magnetic resonance imaging (MRI) for the diagnosis of myocarditis in published cases reports and case series. The localizations were classified as anterior, anterolateral, lateral, inferolateral, inferior, inferoseptal, mid-septal, and anteroseptal. The layers of the myocardium were classified as epicardial or sub-epicardial, mid, and endocardial or sub-endocardial wall.

Generally, myocarditic infiltrations due to viral infection occur in a peculiar pattern (i.e., predominantly in the lateral free wall, originating from the epicardial quartile of the ventricular wall in myocarditis patients) (42). The patterns of LGE occurring in general viral myocarditis as well as in COVID-19 mRNA vaccination-associated myocarditis appear to be similar.

Possible Mechanism of COVID-19 mRNA Vaccination-Associated Myocarditis

The mechanisms mediating COVID-19 mRNA vaccination-associated myocarditis have not been elucidated in detail till date. We suspect that the mechanisms mediating COVID-19 mRNA vaccination-associated myocarditis may be similar to those underlying viral myocarditis. Viral myocarditis is mainly due to direct viral damage and the subsequent IL-6-mediated immune response (43).

The mRNA vaccine mainly elicits a local immune response after being injected intramuscularly. However, this immune response is also present systematically, including in the liver, pancreas, and lymph nodes. In experiments among animal models, lipid nanoparticle-modified mRNA influenza vaccines were distributed mainly in the above mentioned organs, but were also detected to a lesser extent in the heart (44). mRNA vaccines do not cause COVID-19, as the mRNA breaks down rapidly in the cell and the vaccine encodes only a portion of the complete virion. Due to the structural design of the mRNA vaccine, it is uncertain whether distribution of vaccine components to the heart could cause direct damage.

The possibility of immunological mechanisms mediating the development of myocarditis following mRNA vaccination needs to be considered. For example, naive T lymphocytes may be primed by autologous proteins released from damaged cardiomyocytes via antigen-presenting cells. In rare cases, it has been reported that this can cause the migration of primed T lymphocytes into cardiovascular tissue, as well as cell-mediated cytotoxicity and lymphocytic myocarditis (45). Pro-inflammatory cytokines are released, increasing T lymphocyte activation and contributing to myocardial damage (46). In various published cases of vaccine-associated myocarditis, myocarditis was found to develop after the second vaccination. We suspect that T lymphocytes primed by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) proteins primed by the first vaccination may cause myocarditis. We note that the mRNA-based COVID-19 vaccine is a new vaccine that has not been used previously. More comprehensive elucidation of its pathogenesis is desirable to ensure its safety.

Report From the Ministry of Health, Labour and Welfare, Japan

In Japan, suspected myocarditis-associated events, including myocarditis and pericarditis, have been reported more frequently among males in the age groups of 10–19 and 20–29 years (3.69 and 9.62 cases per million, respectively, for combined first and second vaccinations for the Pfizer mRNA-based vaccine; and 28.83 and 25.65 cases per million, respectively, for combined first and second vaccinations for the Moderna mRNA- based vaccine) (47). Based on reports of suspected adverse drug reactions in Japan and overseas, the Japanese Ministry of Health, Labour and Welfare had decided to revise the medical package inserts for mRNA vaccines. More specifically, the Ministry considered issuing an alert in light of the high frequency of myocarditis-associated events in young males. The recommendation of the Pfizer-BioNTech mRNA-based vaccine is being considered for males in their teens and twenties, as the frequency of reports of suspected myocarditis-associated adverse events following vaccination with the Moderna mRNA-based vaccine were clearly higher than the frequency of events following vaccination with the Pfizer-BioNTech mRNA-based vaccine. Those who had received the Modena vaccine in the past would be able to choose the Pfizer-BioNTech vaccine later on.

Clinical Perspective

COVID-19 vaccine-associated cardiomyopathy is frequently reported to develop within 2–3 days following vaccination and presents as chest pain symptomology (44). Elevated myocardial devitalizing enzymes are found in all cases, whereas changes on electrocardiography as well as decreased contraction (left ventricular ejection fraction <50%) on echocardiography have been reported in only 87 and 15% of patients, respectively (44). If chest symptoms are observed following vaccination, it is advisable to consider the possibility of myocarditis and to perform appropriate blood tests and cMRI scans. In the aforementioned CDC report, myocardial biopsy is included as one of the diagnostic criteria for vaccine-associated myocarditis. However, there are few reports regarding relevant pathology findings, likely because the infiltration of inflammatory cells is reduced compared with that in ordinary acute myocarditis; hence, these findings may not lead directly to a definitive diagnosis. There have been many reports on the characteristics of cardiac MRI in evaluating COVID-19 myocarditis, including the current report, and these reports may be more useful and informative in guiding diagnostics and effective clinical decision-making.

In this review, LGE on cardiac MRI was found to be more common on the inferior lateral wall of the left ventricle and relatively less common on the septal side. This finding is similar to existing reports on viral acute myocarditis (14). In viral myocarditis, cases of LGE on the septal side are considered to have a poor prognosis because of its effect on the conduction system of stimulation to the myocardium. In the current review, Case 4, with LGE on the septal side, showed affected atrioventricular conduction and required relatively intensive treatment, and may have the same tendency in COVID-19 vaccine-associated cardiomyopathy. Hence, cardiac MRI may be useful not only for the diagnosis itself, but also with respect to risk stratification. Although most cases occur in young males and the severity of vaccine-associated myocarditis is relatively low in these age groups, cases of cardiac failure have been reported. Thus, based on existing reports, risk stratification should be performed, hospitalization should be considered in some cases, and careful follow-up is always necessary.

Conclusions

Herein, a report on the detailed features of COVID-19 vaccine-associated myocarditis has been presented. It was found that cMRI is minimally invasive and may aid in the diagnosis of myocarditis. LGE on cMRI tends to occur more frequently on the free wall side and relatively less frequently on the septal side, as in viral myocarditis. These findings can guide future epidemiologic research on this topic of immediate public health importance, directly inform medical guidelines, and help in effective clinical decision-making.

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Statements

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving human participants were reviewed and approved by Institutional Review Board of the Japanese Red Cross Musashino Hospital. The patients/participants provided their written informed consent to participate in this study.

Author contributions

KW, TA, and YM contributed principally to writing the manuscript. ST, MT, TK, MK, RN, SO, TL, TH, MN, GN, RM, SN, YN, TN, MG, and TS revised the manuscript. ST selected the cardiac MRI images and drafted an explanation for the images. All authors contributed to the article and approved the submitted version.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Summary

Keywords

cardiac MRI, COVID-19, mRNA vaccination, myocarditis, case series, review, case report

Citation

Watanabe K, Ashikaga T, Maejima Y, Tao S, Terui M, Kishigami T, Kaneko M, Nakajima R, Okata S, Lee T, Horie T, Nagase M, Nitta G, Miyazaki R, Nagamine S, Nagata Y, Nozato T, Goya M and Sasano T (2022) Case Report: Importance of MRI Examination in the Diagnosis and Evaluation of COVID-19 mRNA Vaccination Induced Myocarditis: Our Experience and Literature Review. Front. Cardiovasc. Med. 9:844626. doi: 10.3389/fcvm.2022.844626

Received

28 December 2021

Accepted

28 March 2022

Published

27 April 2022

Volume

9 - 2022

Edited by

Masanori Aikawa, Brigham and Women's Hospital and Harvard Medical School, United States

Reviewed by

Hendrik Tevaearai Stahel, Bern University Hospital, Switzerland; Tetsuro Miyazaki, Juntendo University Urayasu Hospital, Japan

Updates

Copyright

*Correspondence: Keita Watanabe

This article was submitted to General Cardiovascular Medicine, a section of the journal Frontiers in Cardiovascular Medicine

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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