학술논문

Unique Pulmonary Hypertensive Vascular Diseases Associated with Heart and Lung Developmental Defects
Document Type
article
Source
Journal of Cardiovascular Development and Disease, Vol 10, Iss 8, p 333 (2023)
Subject
congenital heart disease
developmental disorders
Fontan circulation
genetic analysis
major aortopulmonary collateral arteries
pulmonary hypertension
Diseases of the circulatory (Cardiovascular) system
RC666-701
Language
English
ISSN
10080333
2308-3425
Abstract
Although pediatric pulmonary hypertension (PH) shares features and mechanisms with adult PH, there are also some significant differences between the two conditions. Segmental PH is a unique pediatric subtype of PH with unclear and/or multifactorial pathophysiological mechanisms, and is often associated with complex congenital heart disease (CHD), pulmonary atresia with ventricular septal defect, and aortopulmonary collateral arteries. Some cases of complex CHD, associated with a single ventricle after Fontan operation, show pathological changes in the small peripheral pulmonary arteries and pulmonary vascular resistance similar to those observed in pulmonary arterial hypertension (PAH). This condition is termed as the pediatric pulmonary hypertensive vascular disease (PPHVD). Recent advances in genetics have identified the genes responsible for PAH associated with developmental defects of the heart and lungs, such as TBX4 and SOX17. Targeted therapies for PAH have been developed; however, their effects on PH associated with developmental heart and lung defects remain to be established. Real-world data analyses on the anatomy, pathophysiology, genetics, and molecular biology of unique PPHVD cases associated with developmental defects of the heart and lungs, using nationwide and/or international registries, should be conducted in order to improve the treatments and prognosis of patients with these types of pediatric PH.