Document Type
Article
Publication Date
4-22-2026
Publication Title
Journal of Cardiovascular Development and Disease
Volume
13
Issue
5
First page number:
1
Last page number:
43
Abstract
Pulmonary hypertension (PH) can be defined as a mean pulmonary artery pressure (mPAP) greater than 20 mm Hg at rest during right heart catheterization (RHC). The reported prevalence of PH throughout the globe has been estimated to impact approximately 1% of the total population, with a majority of those afflicted being women more than men. Numerous etiologies give rise to the pathophysiology of PH, including heart disease (i.e., left-sided heart failure), lung diseases, and other unclear causes related to chronic stages and complications surrounding long-standing pulmonary thromboembolisms, side effects of certain medications, and genetic and environmental factors. Untreated PH can lead to severe morbidities such as cardio-renal syndrome and congestive hepatopathy (cardiac cirrhosis). Management of PH focuses on decreasing pulmonary pressures by using vasodilators such as prostanoids, and phosphodiesterase type 5 (PDE-5) inhibitors, as well as newer treatments such as sotatercept, which inhibits activin signaling, thereby inhibiting excessive cell growth in the pulmonary artery vasculature and down-regulating the pro-proliferative pathways.
Keywords
pulmonary hypertension; pulmonary arterial hypertension; interstitial lung disease; chronic obstructive pulmonary disease; right ventricular systolic pressure; heart failure; sudden cardiac arrest; arrhythmias; chronic thromboembolism; phosphodiesterase inhibitors; sotatercept
Disciplines
Cardiovascular System | Respiratory System
File Format
File Size
3800 KB
Language
English
Rights
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Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.
Repository Citation
Ramazani, N.,
Barnes, L.,
Wong, A.,
Sharma, D.,
Singh, A.,
Lei, K.
(2026).
The New Era of Pulmonary Hypertension: The Dawn of Disease Modification & Therapeutic Modalities.
Journal of Cardiovascular Development and Disease, 13(5),
1-43.
Available at:
http://dx.doi.org/10.3390/jcdd13050174