Journal Article

Chronic biopsy proven post‐COVID myoendocarditis with SARS‐Cov‐2 persistence and high level of antiheart antibodies

Savina, Polina, Novosadov, Vladimir, Kogan, Evgenia, Lutokhina, Yuliya, Ainetdinova, Dilara, Blagova, Olga, Rud', Ruslan, Fomin, Viktor, Kukleva, Anna, Zaitsev, Alexander

2022

Overview

Purpose To study the clinical signs and mechanisms (viral and autoimmune) of myoendocarditis in the long‐term period after COronaVIrus Disease 2019 (COVID‐19). Methods Fourteen patients (nine male, 50.1 ± 10.2 y.o.) with biopsy proven post‐COVID myocarditis were observed. The diagnosis of COVID‐19 was confirmed by IgG seroconversion. The average time of admission after COVID‐19 was 5.5 [2; 10] months. An endomyocardial biopsy (EMB) of the right ventricle was obtained. The biopsy analysis included polymerase chain reaction diagnosis of viral infection, morphological, immunohistochemical (IHC) examination with antibodies to CD3, CD45, CD68, CD20, SARS‐Cov‐2 spike, and nucleocapsid antigens. Coronary atherosclerosis was ruled out in all patients over 40 years. Results The new cardiac symptoms (congestive heart failure 3–4 New York Heart Association class with severe right ventricular involvement, various rhythm, and conduction disturbances) appeared 1–5 months following COVID‐19. Magnetic resonance imaging showed disseminated or focal subepicardial and intramyocardial late gadolinium enhancement, hyperemia, edema, and increased myocardial native T1 relaxation time. Antiheart antibodies levels were increased 3–4 times in 92.9% of patients. The mean left ventricular (LV) ejection fraction (EF) was 28% (24.5; 37.8). Active lymphocytic myocarditis was diagnosed in 12 patients, eosinophilic myocarditis in two patients. SARS‐Cov‐2 RNA was detected in 12 cases (85.7%), in association with parvovirus B19 DNA—in one. Three patients had also endocarditis (infective and nonbacterial, with parietal thrombosis). As a result of steroid and chronic heart failure therapy, the EF increased to 47% (37.5; 52.5). Conclusions COVID‐19 can lead to long‐term severe post‐COVID myoendocarditis, that is characterized by prolonged persistence of coronavirus in cardiomyocytes, endothelium, and macrophages (up to 18 months) in combination with high immune activity. Corticosteroids and anticoagulants should be considered as a treatment option of post‐COVID myoendocarditis.

• Publisher: John Wiley & Sons, Inc,John Wiley and Sons Inc
• Subject: Antibodies / antiheart antibodies / Atherosclerosis / Biopsy / Biopsy - methods / Cardiovascular agents / Cardiovascular disease / Clinical Investigations / Contrast Media / Coronaviruses / COVID-19 / COVID-19 - complications / Development and progression / Edema / Ejection fraction / endomyocardial biopsy / Gadolinium / Health aspects / Heart / Heart Failure / Humans / Hypertension / Immunoglobulin G / Infection / Infections / Lymphocytes / Magnetic resonance imaging / Male / Morphology / Myocarditis / Myocarditis - diagnosis / Myocarditis - etiology / Myocardium - pathology / Patients / Post-Acute COVID-19 Syndrome / post‐COVID endocarditis / post‐COVID myocarditis / Pulmonary arteries / RNA / RNA, Viral / SARS-CoV-2 / Severe acute respiratory syndrome coronavirus 2 / viral persistence