Circulating S100B and Adiponectin in Children Who Underwent Open Heart Surgery and Cardiopulmonary Bypass

Author:

Varrica Alessandro1,Satriano Angela1,Frigiola Alessandro1,Giamberti Alessandro1,Tettamanti Guido1,Anastasia Luigi1ORCID,Conforti Erika1,Gavilanes Antonio D. W.2,Zimmermann Luc J.2,Vles Hans J. S.2,Li Volti Giovanni3,Gazzolo Diego4ORCID

Affiliation:

1. Department of Pediatric Cardiac Surgery IRCCS San Donato Milanese Hospital, Via Morandi 30, 20097 San Donato Milanese, Italy

2. Department of Pediatrics, Neonatology and Child Neurology, Maastricht University, P. Debyelaan 25, 5800 Maastricht, Netherlands

3. Department of Drug Sciences, Section of Biochemistry, University of Catania, Viale A. Doria 6, 95125 Catania, Italy

4. Department of Maternal Fetal and Neonatal Medicine, C. Arrigo Children’s Hospital, Spalto Marengo 46, 15100 Alessandria, Italy

Abstract

Background. S100B protein, previously proposed as a consolidated marker of brain damage in congenital heart disease (CHD) newborns who underwent cardiac surgery and cardiopulmonary bypass (CPB), has been progressively abandoned due to S100B CNS extra-source such as adipose tissue. The present study investigated CHD newborns, if adipose tissue contributes significantly to S100B serum levels.Methods. We conducted a prospective study in 26 CHD infants, without preexisting neurological disorders, who underwent cardiac surgery and CPB in whom blood samples for S100B and adiponectin (ADN) measurement were drawn at five perioperative time-points.Results. S100B showed a significant increase from hospital admission up to 24 h after procedure reaching its maximum peak(P<0.01)during CPB and at the end of the surgical procedure. Moreover, ADN showed a flat pattern and no significant differences(P>0.05)have been found all along perioperative monitoring. ADN/S100B ratio pattern was identical to S100B alone with the higher peak at the end of CPB and remained higher up to 24 h from surgery.Conclusions. The present study provides evidence that, in CHD infants, S100B protein is not affected by an extra-source adipose tissue release as suggested by no changes in circulating ADN concentrations.

Funder

I Colori della Vita Foundation, Italy

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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