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Published in 2022 at "Pulmonary Circulation"
DOI: 10.1002/pul2.12083
Abstract: Abstract Even though pulmonary arterial hypertension (PAH) remains an incurable disease, the combination of PAH‐specific therapies allowed evolving from symptom‐based strategies to others aiming to move patients to low‐risk conditions. Endothelin‐1 (ET‐1) receptor antagonists emerged…
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Keywords:
arterial hypertension;
macitentan;
potent;
pulmonary arterial ... See more keywords
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Published in 2024 at "Journal of Thoracic Disease"
DOI: 10.21037/jtd-24-151
Abstract: Background Connective tissue disease (CTD) is the second most common cause of the pulmonary arterial hypertension (PAH). Currently, clinical data concerning CTD-PAH is scarce. Our study aimed to assess the efficacy and safety of macitentan…
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Keywords:
ctd pah;
disease;
treatment;
macitentan ... See more keywords
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Published in 2022 at "Frontiers in Pharmacology"
DOI: 10.3389/fphar.2021.811700
Abstract: Background: In a long-term event-driven trial, macitentan has demonstrated beneficial time to clinical worsening in patients with pulmonary arterial hypertension (PAH) and reduced PAH-related hospitalization rates compared with placebo. Macitentan is the most recently approved…
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Keywords:
macitentan;
ambrisentan macitentan;
pah patients;
transition ... See more keywords
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Published in 2024 at "Frontiers in Pharmacology"
DOI: 10.3389/fphar.2024.1369489
Abstract: Introduction: Pulmonary arterial hypertension (PAH) is characterised by endothelial dysfunction and pathological vascular remodelling, resulting in the occlusion of pulmonary arteries and arterioles, right ventricular hypertrophy, and eventually fatal heart failure. Targeting the apelin receptor…
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Keywords:
receptor;
macitentan;
right ventricular;
apelin receptor ... See more keywords