“…Pulmonary arterial hypertension, is a condition characterized by an increase in pulmonary vascular resistance, thrombosis formation, pulmonary vascular remodeling [21][22][23][24][25], structural remodeling of the heart [26], right heart dysfunction and widespread loss of pulmonary microvasculature that carries blood from the heart to the lungs. Although in the past ten years, the treatment of PAH had an apparent progress, but the prognosis is still poor.…”