Biomarkers for pediatric pulmonary arterial hypertension: challenges and recommendations

Ozus Lohani1, Kelley L Colvin2, Michael E Yeager2

  • 1Department of Bioengineering, University of Colorado Denver; Department of Pediatrics-Critical Care.

Insights

Pediatric pulmonary arterial hypertension (PAH) is a serious childhood condition. Identifying specific biomarkers in children with PAH is crucial for effective clinical management and improved outcomes.

Area of Science:

  • Pediatric cardiology
  • Pulmonology
  • Biomarker research

Background:

  • Pediatric pulmonary arterial hypertension (PAH) is a rare but severe condition in children.
  • It leads to progressive pulmonary vascular changes and right heart failure.
  • Current treatments are largely based on adult studies, highlighting a need for pediatric-specific approaches.

Purpose of the Study:

  • To review the current status of biomarkers in pediatric PAH.
  • To explore potential future biomarkers for this population.
  • To provide recommendations for biomarker use and interpretation in pediatric PAH management.

Main Methods:

  • Literature review of existing studies on pediatric PAH biomarkers.
  • Analysis of current evidence-based practices derived from adult PAH studies.
  • Discussion of the challenges and opportunities in pediatric biomarker research.

Main Results:

  • Current biomarkers for pediatric PAH are limited and often extrapolated from adult data.
  • There is a significant need for validated, pediatric-specific biomarkers.
  • Biomarkers could aid in diagnosis, risk stratification, and treatment selection.

Conclusions:

  • Biomarkers are essential for advancing the clinical management of pediatric PAH.
  • Further research is needed to identify and validate reliable biomarkers in children.
  • Standardized interpretation and application of biomarkers are key for improving patient care.

Related Concept Videos

Pulmonary Hypertension: Classification and Pathogenesis01:30

Pulmonary Hypertension: Classification and Pathogenesis

Pulmonary hypertension (PH) is a severe health condition in which the mean pulmonary arterial pressure increases to 25 mmHg or more, even when the body is at rest. This high pressure in the blood vessels that transport blood from the heart to the lungs can cause various symptoms, including shortness of breath, can lead to right heart failure, and significantly affect the overall quality of life.
There are various classifications for PH, each relating to different underlying causes and also...
880
Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers01:19

Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers

Cardiac biomarkers are critical in diagnosing, prognosing, and managing cardiovascular diseases. Routine measurement of specific biomarkers such as B-type natriuretic peptide (BNP), C-reactive protein (CRP), and homocysteine (Hcy) is common practice in clinical settings to evaluate heart function and predict cardiovascular events.
These markers indicate stress or strain on the heart muscle:
Natriuretic Peptides (BNP)
Cardiac myocytes produce these hormones in response to ventricular stretching...
781
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers01:26

Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers

Receptor tyrosine kinase inhibitors (TKIs) and calcium channel blockers (CCBs) are two critical categories of drugs employed in the treatment of pulmonary artery hypertension (PAH). PAH is a disease that causes high blood pressure in the pulmonary arteries, resulting in chest pain, fatigue, and shortness of breath.
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
661
Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists01:18

Treatment for Pulmonary Arterial Hypertension: Endothelin Receptor Antagonists

Endothelins (ETs) are potent vasoactive peptides critical in the human body's various physiological and pathological processes. One of the most promising therapeutic strategies for treating pulmonary arterial hypertension (PAH) involves counteracting the effects of these endothelins using a class of drugs known as endothelin receptor antagonists.
ETs are synthesized through a complex sequence of enzymatic steps, primarily involving an enzyme referred to as endothelin-converting enzyme...
568