Correale Michele, Chirivì Francesco, Bevere Ester Maria Lucia, Tricarico Lucia, D'Alto Michele, Badagliacca Roberto, Brunetti Natale D, Vizza Carmine Dario, Ghio Stefano
Cardiothoracic Department, Policlinico Riuniti University Hospital, 71100 Foggia, Italy.
Department of Medical and Surgical Sciences, University of Foggia, 71100 Foggia, Italy.
J Clin Med. 2024 Apr 22;13(8):2444. doi: 10.3390/jcm13082444.
Pulmonary arterial hypertension is a complex pathology whose etiology is still not completely well clarified. The pathogenesis of pulmonary arterial hypertension involves different molecular mechanisms, with endothelial dysfunction playing a central role in disease progression. Both individual genetic predispositions and environmental factors seem to contribute to its onset. To further understand the complex relationship between endothelial and pulmonary hypertension and try to contribute to the development of future therapies, we report a comprehensive and updated review on endothelial function in pulmonary arterial hypertension.
肺动脉高压是一种复杂的病理状态,其病因仍未完全明确。肺动脉高压的发病机制涉及不同的分子机制,其中内皮功能障碍在疾病进展中起核心作用。个体遗传易感性和环境因素似乎都对其发病有影响。为了进一步了解内皮与肺动脉高压之间的复杂关系,并努力为未来治疗方法的发展做出贡献,我们报告了一篇关于肺动脉高压内皮功能的全面且最新的综述。