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Circulating S100B and Adiponectin in Children Who Underwent Open Heart Surgery and Cardiopulmonary Bypass
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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4568346/ https://www.ncbi.nlm.nih.gov/pubmed/26417594 http://dx.doi.org/10.1155/2015/402642 |
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author | Varrica, Alessandro Satriano, Angela Frigiola, Alessandro Giamberti, Alessandro Tettamanti, Guido Anastasia, Luigi Conforti, Erika Gavilanes, Antonio D. W. Zimmermann, Luc J. Vles, Hans J. S. Li Volti, Giovanni Gazzolo, Diego |
author_facet | Varrica, Alessandro Satriano, Angela Frigiola, Alessandro Giamberti, Alessandro Tettamanti, Guido Anastasia, Luigi Conforti, Erika Gavilanes, Antonio D. W. Zimmermann, Luc J. Vles, Hans J. S. Li Volti, Giovanni Gazzolo, Diego |
author_sort | Varrica, Alessandro |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4568346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-45683462015-09-28 Circulating S100B and Adiponectin in Children Who Underwent Open Heart Surgery and Cardiopulmonary Bypass Varrica, Alessandro Satriano, Angela Frigiola, Alessandro Giamberti, Alessandro Tettamanti, Guido Anastasia, Luigi Conforti, Erika Gavilanes, Antonio D. W. Zimmermann, Luc J. Vles, Hans J. S. Li Volti, Giovanni Gazzolo, Diego Biomed Res Int Clinical Study 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. Hindawi Publishing Corporation 2015 2015-08-31 /pmc/articles/PMC4568346/ /pubmed/26417594 http://dx.doi.org/10.1155/2015/402642 Text en Copyright © 2015 Alessandro Varrica et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Varrica, Alessandro Satriano, Angela Frigiola, Alessandro Giamberti, Alessandro Tettamanti, Guido Anastasia, Luigi Conforti, Erika Gavilanes, Antonio D. W. Zimmermann, Luc J. Vles, Hans J. S. Li Volti, Giovanni Gazzolo, Diego Circulating S100B and Adiponectin in Children Who Underwent Open Heart Surgery and Cardiopulmonary Bypass |
title | Circulating S100B and Adiponectin in Children Who Underwent Open Heart Surgery and Cardiopulmonary Bypass |
title_full | Circulating S100B and Adiponectin in Children Who Underwent Open Heart Surgery and Cardiopulmonary Bypass |
title_fullStr | Circulating S100B and Adiponectin in Children Who Underwent Open Heart Surgery and Cardiopulmonary Bypass |
title_full_unstemmed | Circulating S100B and Adiponectin in Children Who Underwent Open Heart Surgery and Cardiopulmonary Bypass |
title_short | Circulating S100B and Adiponectin in Children Who Underwent Open Heart Surgery and Cardiopulmonary Bypass |
title_sort | circulating s100b and adiponectin in children who underwent open heart surgery and cardiopulmonary bypass |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4568346/ https://www.ncbi.nlm.nih.gov/pubmed/26417594 http://dx.doi.org/10.1155/2015/402642 |
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