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Updated: May 15, 2026

Increasing Pulmonary Artery Pulsatile Flow Improves Hypoxic Pulmonary Hypertension in Piglets
Published on: May 11, 2015
Circulating cytokines and growth factors in pediatric pulmonary hypertension
Mark Duncan1, Brandie D Wagner, Keri Murray
1Section of Pediatric Pulmonology, School of Medicine, University of Colorado and Children's Hospital Colorado, Aurora, CO 80045, USA. mark.duncan@ucdenver.edu
Insights
Circulating proteins like VEGF and IL-6 show promise as biomarkers for pediatric pulmonary hypertension (PH). Measuring these proteins may help predict adverse events and guide treatment for children with PH.
Area of Science:
- Cardiology
- Pulmonology
- Biomarker Discovery
Background:
- Pediatric pulmonary hypertension (PH) management is challenging.
- Identifying reliable biomarkers is crucial for predicting outcomes.
- Noninvasive tools are needed to aid in pediatric PH management.
Purpose of the Study:
- To assess circulating proteins as predictive and prognostic biomarkers in pediatric PH.
- To investigate the association between protein markers and hemodynamic variables.
- To develop a practical, noninvasive tool for managing pediatric PH.
Main Methods:
- Analyzed 12 cytokines and growth factors in plasma from 70 children with PH.
- Utilized multiplex protein array technology.
- Evaluated associations between hemodynamics, adverse events, and protein markers.
Main Results:
- Epidermal growth factor (EGF) and IL-6 correlated with key hemodynamics.
- VEGF and IL-6 were significantly associated with adverse events (ORs: 0.56 and 1.69, respectively).
- Combining hemodynamic predictors with protein markers improved adverse outcome prediction.
Conclusions:
- Specific circulating proteins are linked to hemodynamic variables in pediatric PH.
- These protein markers could aid patient care and clinical trial design by identifying at-risk individuals.
- Findings suggest a role for inflammation in the pathophysiology of pediatric PH.
Background:
Management of pediatric pulmonary hypertension (PH) remains challenging. We have assessed a panel of circulating proteins in children with PH to investigate their value as predictive and/or prognostic biomarkers. From these determinations, we aim to develop a practical, noninvasive tool to aid in the management of pediatric PH.
Methods:
Twelve cytokines and growth factors putatively associated with lung or vascular disease were examined in plasma specimens from 70 children with PH using multiplex protein array technology. Associations between hemodynamics, adverse events, and protein markers were evaluated.
Results:
Epidermal growth factor (EGF) and IL-6 were associated with important hemodynamics. Of the twelve proteins, VEGF and IL-6 were significantly, univariately associated with the occurrence of an adverse event, with odds ratios (95% confidence intervals) of 0.56 (0.33-0.98) and 1.69 (1.03-2.77), respectively. When hemodynamic predictors were combined with protein markers, the ability to predict adverse outcomes within the following year significantly increased.
Conclusions:
Specific circulating proteins are associated with hemodynamic variables in pediatric PH. If confirmed in additional cohorts, measurement of these proteins could aid patient care and design of clinical trials by identifying patients at risk for adverse events. These findings also further support a role for inflammation in pediatric PH.
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