Altered metabolic and inflammatory transcriptomics after cardiac surgery in neonates with congenital heart disease

• Published in: Scientific reports Vol. 11; no. 1; p. 4965
• Main Authors: Jain, Parag N., Robertson, Matthew, Lasa, Javier J., Shekerdemian, Lara, Guffey, Danielle, Zhang, Yuhao, Lingappan, Krithika, Checchia, Paul, Coarfa, Cristian
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 02.03.2021; Nature Publishing Group; Nature Portfolio
• Subjects: 631/208/212/2019; 692/4019/592/2727; 692/4019/592/75/1539; 692/4019/592/75/230; Amino acids; Aorta; Blood; Cardiovascular disease; Cardiovascular diseases; Congenital diseases; Coronary artery disease; Electron transport chain; G protein-coupled receptors; Gene expression; Heart diseases; Heart surgery; Heme; Humanities and Social Sciences; Inflammation; Metabolic pathways; Metabolism; multidisciplinary; Neonates; Nerve growth factor; Notch1 protein; Oxidative metabolism; Oxidative phosphorylation; Phosphorylation; Platelet-derived growth factor; Protein turnover; Science; Science (multidisciplinary); Surgery; Transcriptomes; Tricarboxylic acid cycle
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-83882-x

The study examines the whole blood transcriptome profile before and after cardiopulmonary bypass (CPB) in neonates with hypoplastic left heart syndrome (HLHS), a severe form of congenital heart disease, that can develop low cardiac output syndrome (LCOS). Whole blood mRNA transcriptome profiles of 13 neonates with HLHS before and after their first palliative surgery were analyzed to determine differentially expressed genes and pathways. The median age and weight at surgery were 4 days and 3.2 kg, respectively. Of the 13 patients, 8 developed LCOS. There was no significant difference between CPB, aortic cross clamp, deep hypothermic cardiac arrest times between patients that develop LCOS and those that do not. Upon comparing differential gene expression profiles between patients that develop LCOS and those that do not in pre-operative samples, 1 gene was up-regulated and 13 were down regulated. In the post-operative samples, 4 genes were up-regulated, and 4 genes were down regulated when patients that develop LCOS were compared to those that do not. When comparing post-operative samples to pre-operative samples in the patients that do not develop LCOS, 1484 genes were up-regulated, and 1388 genes were down regulated; while patients that developed LCOS had 2423 up-regulated genes, and 2414 down regulated genes for the same pre to post-operative comparison. Pathway analysis revealed differential regulation of inflammatory pathways (IL signaling, PDGF, NOTCH1, NGF, GPCR) and metabolic pathways (heme metabolism, oxidative phosphorylation, protein metabolism including amino acid and derivatives, fatty acid metabolism, TCA cycle and respiratory electron transport chain). By identifying altered transcriptome profiles related to inflammation and metabolism in neonates with HLHS who develop LCOS after CPB, this study opens for exploration novel pathways and potential therapeutic targets to improve outcomes in this high-risk population.