Cargando…

Plasma proteoglycan 4: a novel biomarker for acute lung injury after pediatric cardiac surgery

BACKGROUND: Identification of biological molecules related to post cardiopulmonary bypass (CPB) lung injury could help diagnose, predict and potentially impact patient’s clinical course after cardiac surgery. Proteoglycan 4 (PRG4) initially identified as potential biomarker for patients with prolong...

Descripción completa

Detalles Bibliográficos
Autores principales: Asfari, Ahmed, Doyle, Erica A., Jay, Gregory D., Aristizabal, Natalia, Manchikalapati, Ananya, Rahman, A. K. M. Fazlur, Hock, Kristal M., Borasino, Santiago, Ambalavanan, Namasivayam, Schmidt, Tannin A., Rhodes, Leslie A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560364/
https://www.ncbi.nlm.nih.gov/pubmed/37814710
http://dx.doi.org/10.21037/tp-23-194
_version_ 1785117717455437824
author Asfari, Ahmed
Doyle, Erica A.
Jay, Gregory D.
Aristizabal, Natalia
Manchikalapati, Ananya
Rahman, A. K. M. Fazlur
Hock, Kristal M.
Borasino, Santiago
Ambalavanan, Namasivayam
Schmidt, Tannin A.
Rhodes, Leslie A.
author_facet Asfari, Ahmed
Doyle, Erica A.
Jay, Gregory D.
Aristizabal, Natalia
Manchikalapati, Ananya
Rahman, A. K. M. Fazlur
Hock, Kristal M.
Borasino, Santiago
Ambalavanan, Namasivayam
Schmidt, Tannin A.
Rhodes, Leslie A.
author_sort Asfari, Ahmed
collection PubMed
description BACKGROUND: Identification of biological molecules related to post cardiopulmonary bypass (CPB) lung injury could help diagnose, predict and potentially impact patient’s clinical course after cardiac surgery. Proteoglycan 4 (PRG4) initially identified as potential biomarker for patients with prolonged mechanical ventilation following CPB in a prior study. To further validate these findings, we sought to understand the association of lower plasma PRG4 with prolonged mechanical ventilation and worse lung compliance in a larger cohort of pediatric patients post CPB. METHODS: Retrospective chart review study. Pediatric Cardiac Intensive Care Unit, Tertiary Hospital. Infants <1 year old with tetralogy of Fallot, ventricular septal defect, or atrioventricular septal defect who underwent surgical repair 2012–2020 and had stored plasma samples in our biorepository were screened for inclusion. Patients with mechanical ventilation before surgery were excluded. Patients were divided into quartiles based on postoperative duration of mechanical ventilation (control <25(th) percentile, study >75(th) percentile). Preoperative and 48-hour postoperative samples for each cohort (20 patients each) were tested for PRG4 level using enzyme-linked immunosorbent assay (ELISA) technique. RESULTS: Study group had lower lung compliance, higher mean airway pressure and higher oxygen need postoperative when compared to control group. Plasma PRG4 levels before surgery and 48 hours postoperative were lower in study group compared to control group (P=0.0232 preoperative; P=0.0016 postoperative). Plasma PRG4 levels were compared preoperative to PRG4 levels postoperative in both group, there was no statistically significant difference (study group: P=0.0869; control group: P=0.6500) CONCLUSIONS: Lower levels of plasma PRG4 is associated with longer duration of mechanical ventilation, worse ventilator compliance and higher oxygen requirement after cardiac surgery in our patient population. Further validation of this finding in a larger and more diverse patient population is necessary prior to its application at the bedside.
format Online
Article
Text
id pubmed-10560364
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher AME Publishing Company
record_format MEDLINE/PubMed
spelling pubmed-105603642023-10-09 Plasma proteoglycan 4: a novel biomarker for acute lung injury after pediatric cardiac surgery Asfari, Ahmed Doyle, Erica A. Jay, Gregory D. Aristizabal, Natalia Manchikalapati, Ananya Rahman, A. K. M. Fazlur Hock, Kristal M. Borasino, Santiago Ambalavanan, Namasivayam Schmidt, Tannin A. Rhodes, Leslie A. Transl Pediatr Original Article BACKGROUND: Identification of biological molecules related to post cardiopulmonary bypass (CPB) lung injury could help diagnose, predict and potentially impact patient’s clinical course after cardiac surgery. Proteoglycan 4 (PRG4) initially identified as potential biomarker for patients with prolonged mechanical ventilation following CPB in a prior study. To further validate these findings, we sought to understand the association of lower plasma PRG4 with prolonged mechanical ventilation and worse lung compliance in a larger cohort of pediatric patients post CPB. METHODS: Retrospective chart review study. Pediatric Cardiac Intensive Care Unit, Tertiary Hospital. Infants <1 year old with tetralogy of Fallot, ventricular septal defect, or atrioventricular septal defect who underwent surgical repair 2012–2020 and had stored plasma samples in our biorepository were screened for inclusion. Patients with mechanical ventilation before surgery were excluded. Patients were divided into quartiles based on postoperative duration of mechanical ventilation (control <25(th) percentile, study >75(th) percentile). Preoperative and 48-hour postoperative samples for each cohort (20 patients each) were tested for PRG4 level using enzyme-linked immunosorbent assay (ELISA) technique. RESULTS: Study group had lower lung compliance, higher mean airway pressure and higher oxygen need postoperative when compared to control group. Plasma PRG4 levels before surgery and 48 hours postoperative were lower in study group compared to control group (P=0.0232 preoperative; P=0.0016 postoperative). Plasma PRG4 levels were compared preoperative to PRG4 levels postoperative in both group, there was no statistically significant difference (study group: P=0.0869; control group: P=0.6500) CONCLUSIONS: Lower levels of plasma PRG4 is associated with longer duration of mechanical ventilation, worse ventilator compliance and higher oxygen requirement after cardiac surgery in our patient population. Further validation of this finding in a larger and more diverse patient population is necessary prior to its application at the bedside. AME Publishing Company 2023-09-11 2023-09-18 /pmc/articles/PMC10560364/ /pubmed/37814710 http://dx.doi.org/10.21037/tp-23-194 Text en 2023 Translational Pediatrics. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Asfari, Ahmed
Doyle, Erica A.
Jay, Gregory D.
Aristizabal, Natalia
Manchikalapati, Ananya
Rahman, A. K. M. Fazlur
Hock, Kristal M.
Borasino, Santiago
Ambalavanan, Namasivayam
Schmidt, Tannin A.
Rhodes, Leslie A.
Plasma proteoglycan 4: a novel biomarker for acute lung injury after pediatric cardiac surgery
title Plasma proteoglycan 4: a novel biomarker for acute lung injury after pediatric cardiac surgery
title_full Plasma proteoglycan 4: a novel biomarker for acute lung injury after pediatric cardiac surgery
title_fullStr Plasma proteoglycan 4: a novel biomarker for acute lung injury after pediatric cardiac surgery
title_full_unstemmed Plasma proteoglycan 4: a novel biomarker for acute lung injury after pediatric cardiac surgery
title_short Plasma proteoglycan 4: a novel biomarker for acute lung injury after pediatric cardiac surgery
title_sort plasma proteoglycan 4: a novel biomarker for acute lung injury after pediatric cardiac surgery
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560364/
https://www.ncbi.nlm.nih.gov/pubmed/37814710
http://dx.doi.org/10.21037/tp-23-194
work_keys_str_mv AT asfariahmed plasmaproteoglycan4anovelbiomarkerforacutelunginjuryafterpediatriccardiacsurgery
AT doyleericaa plasmaproteoglycan4anovelbiomarkerforacutelunginjuryafterpediatriccardiacsurgery
AT jaygregoryd plasmaproteoglycan4anovelbiomarkerforacutelunginjuryafterpediatriccardiacsurgery
AT aristizabalnatalia plasmaproteoglycan4anovelbiomarkerforacutelunginjuryafterpediatriccardiacsurgery
AT manchikalapatiananya plasmaproteoglycan4anovelbiomarkerforacutelunginjuryafterpediatriccardiacsurgery
AT rahmanakmfazlur plasmaproteoglycan4anovelbiomarkerforacutelunginjuryafterpediatriccardiacsurgery
AT hockkristalm plasmaproteoglycan4anovelbiomarkerforacutelunginjuryafterpediatriccardiacsurgery
AT borasinosantiago plasmaproteoglycan4anovelbiomarkerforacutelunginjuryafterpediatriccardiacsurgery
AT ambalavanannamasivayam plasmaproteoglycan4anovelbiomarkerforacutelunginjuryafterpediatriccardiacsurgery
AT schmidttannina plasmaproteoglycan4anovelbiomarkerforacutelunginjuryafterpediatriccardiacsurgery
AT rhodeslesliea plasmaproteoglycan4anovelbiomarkerforacutelunginjuryafterpediatriccardiacsurgery