TY - JOUR
T1 - Cardiopulmonary Bypass-Induced Inflammation and Myocardial Ischemia and Reperfusion Injury Stimulates Accumulation of Soluble MER∗
AU - Becker, Amanda C.
AU - Lantz, Connor W.
AU - Forbess, Joseph M.
AU - Epting, Conrad L.
AU - Thorp, Edward B.
N1 - Funding Information:
Supported, in part, by the Sidney and Bess Eisenberg Memorial Fund.
Funding Information:
Dr. Becker received internal grant support from a Pediatric Critical Care Fellow Research Award through Ann & Robert H. Lurie Children’s Hospital of Chicago. Mr. Lantz is supported by the National Institutes of Health (NIH) T32 GM008061. Dr. Thorp is supported by NIH R01-HL122309, HL139812, and P01AI112522. The remaining authors have disclosed that they do not have any potential conflicts of interest.
Publisher Copyright:
© 2021 Lippincott Williams and Wilkins. All rights reserved.
PY - 2021/9/1
Y1 - 2021/9/1
N2 - Objectives: Soluble MER has emerged as a potential biomarker for delayed resolution of inflammation after myocardial injury and a therapeutic target to reduce cardiac-related morbidity and mortality in adults. The significance of soluble MER in pediatric populations, however, is unclear. We sought to investigate if soluble MER concentrations change in response to myocardial ischemia and reperfusion injury in pediatric patients. In parallel, we also sought to investigate for correlations between the change in soluble MER concentration and specific patient, bypass, and postoperative data. Design: We quantified the change in plasma soluble MER concentration post- compared with precardiopulmonary bypass for each patient in a cohort of pediatric patients. Linear regression, correlation coefficients, and t tests were used to compare innate patient characteristics (i.e., sex, age, cyanotic vs acyanotic cardiac lesion), cardiac bypass data (i.e., total cardiac bypass time, total aortic cross-clamp time, perioperative steroid administration), and postcardiac bypass data (total postoperative ventilator days, total postoperative vasoactive medication days, and total postoperative ICU days) with change in soluble MER concentrations. Setting: Whole blood samples were obtained intraoperatively at a single tertiary care children's hospital from April to October 2019. Subjects: Our patient cohort included 24 pediatric patients ages ranging from birth to 19 years old with both cyanotic and acyanotic cardiac lesions. Interventions: Retrospective analyses of pediatric blood specimens, as well as patient, bypass, and postoperative data, were performed. Measurements and Main Results: We observed a statistically significant increase in soluble MER concentration post cardiac bypass in 17 of 24 patients (71%). Conclusions: Soluble MER concentrations increase with cardiopulmonary bypass-induced inflammation and myocardial ischemia and reperfusion injury in pediatric patients. The utility of soluble MER as a clinical biomarker to identify pediatric patients at risk for exacerbated postoperative outcomes after bypass-induced myocardial ischemia and reperfusion injury requires further investigation.
AB - Objectives: Soluble MER has emerged as a potential biomarker for delayed resolution of inflammation after myocardial injury and a therapeutic target to reduce cardiac-related morbidity and mortality in adults. The significance of soluble MER in pediatric populations, however, is unclear. We sought to investigate if soluble MER concentrations change in response to myocardial ischemia and reperfusion injury in pediatric patients. In parallel, we also sought to investigate for correlations between the change in soluble MER concentration and specific patient, bypass, and postoperative data. Design: We quantified the change in plasma soluble MER concentration post- compared with precardiopulmonary bypass for each patient in a cohort of pediatric patients. Linear regression, correlation coefficients, and t tests were used to compare innate patient characteristics (i.e., sex, age, cyanotic vs acyanotic cardiac lesion), cardiac bypass data (i.e., total cardiac bypass time, total aortic cross-clamp time, perioperative steroid administration), and postcardiac bypass data (total postoperative ventilator days, total postoperative vasoactive medication days, and total postoperative ICU days) with change in soluble MER concentrations. Setting: Whole blood samples were obtained intraoperatively at a single tertiary care children's hospital from April to October 2019. Subjects: Our patient cohort included 24 pediatric patients ages ranging from birth to 19 years old with both cyanotic and acyanotic cardiac lesions. Interventions: Retrospective analyses of pediatric blood specimens, as well as patient, bypass, and postoperative data, were performed. Measurements and Main Results: We observed a statistically significant increase in soluble MER concentration post cardiac bypass in 17 of 24 patients (71%). Conclusions: Soluble MER concentrations increase with cardiopulmonary bypass-induced inflammation and myocardial ischemia and reperfusion injury in pediatric patients. The utility of soluble MER as a clinical biomarker to identify pediatric patients at risk for exacerbated postoperative outcomes after bypass-induced myocardial ischemia and reperfusion injury requires further investigation.
KW - cardiopulmonary bypass
KW - myocardial ischemia/reperfusion injury
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U2 - 10.1097/PCC.0000000000002725
DO - 10.1097/PCC.0000000000002725
M3 - Article
C2 - 33813548
AN - SCOPUS:85115036445
SN - 1529-7535
VL - 22
SP - 822
EP - 831
JO - Pediatric Critical Care Medicine
JF - Pediatric Critical Care Medicine
IS - 9
ER -