Skewed Cytokine Responses Rather Than the Magnitude of the Cytokine Storm May Drive Cardiac Dysfunction in Multisystem Inflammatory Syndrome in Children

Background Cardiac dysfunction is a prominent feature of multisystem inflammatory syndrome in children (MIS‐C), yet the etiology is poorly understood. We determined whether dysfunction is global or regional, and whether it is associated with the cytokine milieu, microangiopathy, or severity of shock...

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Main Authors: Joyce C. Chang, Daisuke Matsubara, Ryan W. Morgan, Caroline Diorio, Sumekala Nadaraj, David T. Teachey, Hamid Bassiri, Edward M. Behrens, Anirban Banerjee
Format: Article
Language:English
Published: Wiley 2021-08-01
Series:Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Subjects:
Online Access:https://www.ahajournals.org/doi/10.1161/JAHA.121.021428
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author Joyce C. Chang
Daisuke Matsubara
Ryan W. Morgan
Caroline Diorio
Sumekala Nadaraj
David T. Teachey
Hamid Bassiri
Edward M. Behrens
Anirban Banerjee
author_facet Joyce C. Chang
Daisuke Matsubara
Ryan W. Morgan
Caroline Diorio
Sumekala Nadaraj
David T. Teachey
Hamid Bassiri
Edward M. Behrens
Anirban Banerjee
author_sort Joyce C. Chang
collection DOAJ
description Background Cardiac dysfunction is a prominent feature of multisystem inflammatory syndrome in children (MIS‐C), yet the etiology is poorly understood. We determined whether dysfunction is global or regional, and whether it is associated with the cytokine milieu, microangiopathy, or severity of shock. Methods and Results We analyzed echocardiographic parameters of myocardial deformation and compared global and segmental left ventricular strain between 43 cases with MIS‐C ≤18 years old and 40 controls. Primary outcomes included left ventricular global longitudinal strain, right ventricular free wall strain), and left atrial strain. We evaluated relationships between strain and profiles of 10 proinflammatory cytokines, microangiopathic features (soluble C5b9), and vasoactive‐inotropic requirements. Compared with controls, cases with MIS‐C had significant impairments in all parameters of systolic and diastolic function. 65% of cases with MIS‐C had abnormal left ventricular function (|global longitudinal strain|<17%), although elevations of cytokines were modest. All left ventricular segments were involved, without apical or basal dominance to suggest acute stress cardiomyopathy. Worse global longitudinal strain correlated with higher ratios of interleukin‐6 (ρ −0.43) and interleukin‐8 (ρ −0.43) to total hypercytokinemia, but not absolute levels of interleukin‐6 or interleukin‐8, or total hypercytokinemia. Similarly, worse right ventricular free wall strain correlated with higher relative interleukin‐8 expression (ρ −0.59). There were no significant associations between function and microangiopathy or vasoactive‐inotropic requirements. Conclusions Myocardial function is globally decreased in MIS‐C and not explained by acute stress cardiomyopathy. Cardiac dysfunction may be driven by the relative skew of the immune response toward interleukin‐6 and interleukin‐8 pathways, more so than degree of hyperinflammation, refining the current paradigm of myocardial involvement in MIS‐C.
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spelling doaj.art-a95b054e755c408ca84d32a9616c7ee82023-06-06T12:10:51ZengWileyJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease2047-99802021-08-01101610.1161/JAHA.121.021428Skewed Cytokine Responses Rather Than the Magnitude of the Cytokine Storm May Drive Cardiac Dysfunction in Multisystem Inflammatory Syndrome in ChildrenJoyce C. Chang0Daisuke Matsubara1Ryan W. Morgan2Caroline Diorio3Sumekala Nadaraj4David T. Teachey5Hamid Bassiri6Edward M. Behrens7Anirban Banerjee8Division of Rheumatology Children's Hospital of Philadelphia PADivision of Cardiology Children's Hospital of Philadelphia PADivision of Critical Care Medicine Children's Hospital of Philadelphia PADepartment of Pediatrics University of Pennsylvania Perelman School of Medicine Philadelphia PADivision of Cardiology Children's Hospital of Philadelphia PADepartment of Pediatrics University of Pennsylvania Perelman School of Medicine Philadelphia PADepartment of Pediatrics University of Pennsylvania Perelman School of Medicine Philadelphia PADivision of Rheumatology Children's Hospital of Philadelphia PADepartment of Pediatrics University of Pennsylvania Perelman School of Medicine Philadelphia PABackground Cardiac dysfunction is a prominent feature of multisystem inflammatory syndrome in children (MIS‐C), yet the etiology is poorly understood. We determined whether dysfunction is global or regional, and whether it is associated with the cytokine milieu, microangiopathy, or severity of shock. Methods and Results We analyzed echocardiographic parameters of myocardial deformation and compared global and segmental left ventricular strain between 43 cases with MIS‐C ≤18 years old and 40 controls. Primary outcomes included left ventricular global longitudinal strain, right ventricular free wall strain), and left atrial strain. We evaluated relationships between strain and profiles of 10 proinflammatory cytokines, microangiopathic features (soluble C5b9), and vasoactive‐inotropic requirements. Compared with controls, cases with MIS‐C had significant impairments in all parameters of systolic and diastolic function. 65% of cases with MIS‐C had abnormal left ventricular function (|global longitudinal strain|<17%), although elevations of cytokines were modest. All left ventricular segments were involved, without apical or basal dominance to suggest acute stress cardiomyopathy. Worse global longitudinal strain correlated with higher ratios of interleukin‐6 (ρ −0.43) and interleukin‐8 (ρ −0.43) to total hypercytokinemia, but not absolute levels of interleukin‐6 or interleukin‐8, or total hypercytokinemia. Similarly, worse right ventricular free wall strain correlated with higher relative interleukin‐8 expression (ρ −0.59). There were no significant associations between function and microangiopathy or vasoactive‐inotropic requirements. Conclusions Myocardial function is globally decreased in MIS‐C and not explained by acute stress cardiomyopathy. Cardiac dysfunction may be driven by the relative skew of the immune response toward interleukin‐6 and interleukin‐8 pathways, more so than degree of hyperinflammation, refining the current paradigm of myocardial involvement in MIS‐C.https://www.ahajournals.org/doi/10.1161/JAHA.121.021428COVID‐19cytokine stormechocardiographymultisystem inflammatory syndrome in childrenmyocardial deformation
spellingShingle Joyce C. Chang
Daisuke Matsubara
Ryan W. Morgan
Caroline Diorio
Sumekala Nadaraj
David T. Teachey
Hamid Bassiri
Edward M. Behrens
Anirban Banerjee
Skewed Cytokine Responses Rather Than the Magnitude of the Cytokine Storm May Drive Cardiac Dysfunction in Multisystem Inflammatory Syndrome in Children
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
COVID‐19
cytokine storm
echocardiography
multisystem inflammatory syndrome in children
myocardial deformation
title Skewed Cytokine Responses Rather Than the Magnitude of the Cytokine Storm May Drive Cardiac Dysfunction in Multisystem Inflammatory Syndrome in Children
title_full Skewed Cytokine Responses Rather Than the Magnitude of the Cytokine Storm May Drive Cardiac Dysfunction in Multisystem Inflammatory Syndrome in Children
title_fullStr Skewed Cytokine Responses Rather Than the Magnitude of the Cytokine Storm May Drive Cardiac Dysfunction in Multisystem Inflammatory Syndrome in Children
title_full_unstemmed Skewed Cytokine Responses Rather Than the Magnitude of the Cytokine Storm May Drive Cardiac Dysfunction in Multisystem Inflammatory Syndrome in Children
title_short Skewed Cytokine Responses Rather Than the Magnitude of the Cytokine Storm May Drive Cardiac Dysfunction in Multisystem Inflammatory Syndrome in Children
title_sort skewed cytokine responses rather than the magnitude of the cytokine storm may drive cardiac dysfunction in multisystem inflammatory syndrome in children
topic COVID‐19
cytokine storm
echocardiography
multisystem inflammatory syndrome in children
myocardial deformation
url https://www.ahajournals.org/doi/10.1161/JAHA.121.021428
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