Key result
Elevated DBH, ADIPO, and ANPEP are linked to PAH in VSD, enabling a new risk score.
Why the study?
The molecular mechanisms underlying pulmonary arterial hypertension in congenital ventricular septal defects are unclear, necessitating identification of molecular pathways and biomarkers.
Does a multi-omics-derived protein risk score (DBH, ANPEP, ADIPO) predict the occurrence of pulmonary arterial hypertension in children with ventricular septal defects?
Observational (n=240)
Does a multi-omics-derived protein risk score (DBH, ANPEP, ADIPO) predict the occurrence of pulmonary arterial hypertension in children with ventricular septal defects?
A novel risk score based on plasma levels of DBH, ANPEP, and ADIPO may serve as a biomarker for predicting pulmonary arterial hypertension in children with ventricular septal defects.
May support a biomarker panel for PAH risk in pediatric VSD; leaves open prospective validation before clinical use.
The molecular mechanisms underlying pulmonary arterial hypertension (PAH) in congenital ventricular septal defects (VSD) are unclear. We aimed to reveal molecular pathways and potential biomarkers by multi-omics analysis in VSD-PAH. Plasma from 160 children, including 120 VSD patients with/without PAH and 40 healthy children was studied by integrated proteomics, metabolomics, and bioinformatics analyses. Proteomics identified 107 differential proteins (DPs) between patients with/without PAH including significantly increased adiponectin (ADIPO), dopamine β-hydroxylase (DBH), alanyl membrane aminopeptidase (ANPEP), transferrin receptor 1, and glycoprotein Ib platelet α-subunit and decreased guanine nucleotide-binding protein Gs in VSD-PAH. Metabolomics discovered 191 differential metabolites between patients with/without PAH, including elevation of serotonin, taurine, creatine, sarcosine, and 2-oxobutanoate, and decrease of vanillylmandelic acid, 3,4-dihydroxymandelate, 15-keto-prostaglandin F 2α, fructose 6-phosphate, l-glutamine, dehydroascorbate, hydroxypyruvate, threonine, l-cystine, and 1-aminocyclopropane-1-carboxylate. The DPs were validated in a new cohort of patients ( n = 80). Integrated analyses identified key pathways, including cAMP, ECM receptor interaction, AMPK, hypoxia-inducible factor 1, PI3K-Akt signaling pathways, and amino acid metabolisms. Increased plasma protein levels of DBH, ADIPO, and ANPEP were found to be independently associated with the occurrence of PAH, with a new total risk score from these three proteins developed for clinical diagnosis. In this integrated multi-omics analysis in VSD-PAH patients, we have, for the first time, found that VSD-PAH patients present important differential proteins, metabolites, and key pathways. We have developed a total risk score (based on the plasma concentration of DBH, ANPEP, and ADIPO) as a predictor of development of PAH in CHD-VSD patients. Therefore, these proteins may be used as biomarkers, and the new total risk score has significant clinical implications in the diagnosis of PAH.
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Yuan et al. (2020) conducted an observational in Pulmonary arterial hypertension associated with ventricular septal defect (n=240). Plasma protein biomarkers (DBH, ADIPO, ANPEP) vs. VSD without PAH and healthy controls was evaluated on Occurrence of pulmonary arterial hypertension. Increased plasma levels of DBH, ADIPO, and ANPEP were independently associated with the occurrence of PAH in children with VSD, enabling a new diagnostic risk score.
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