Menezes Thaís C F, Lee Michael H, Fonseca Balladares Dara C, Nolan Kevin, Sharma Sankalp, Kumar Rahul, Ferreira Eloara V M, Graham Brian B, Oliveira Rudolf K F
Division of Respiratory Diseases, Department of Medicine, Hospital São Paulo Federal University of São Paulo (UNIFESP) São Paulo Brazil.
Division of Pulmonary and Critical Care Medicine, Department of Medicine University of California, San Francisco San Francisco CA USA.
J Am Heart Assoc. 2025 Feb 18;14(4):e036952. doi: 10.1161/JAHA.124.036952. Epub 2025 Feb 8.
Pulmonary arterial hypertension is a disease of the pulmonary vasculature, resulting in elevated pressure in the pulmonary arteries and disrupting the physiological coordination between the right heart and the pulmonary circulation. Exercise intolerance is one of the primary symptons of pulmonary arterial hypertension, significantly impacting the quality of life. The pathophysiology of exercise intolerance in pulmonary arterial hypertension is complex and likely multifactorial. Although the significance of right ventricle impairment and perfusion/ventilation mismatch is widely acknowledged, recent studies suggest pathophysiology of the skeletal muscle contributes to reduced exercise capacity in pulmonary arterial hypertension, a concept explored herein.
肺动脉高压是一种肺血管疾病,会导致肺动脉压力升高,并破坏右心与肺循环之间的生理协调。运动不耐受是肺动脉高压的主要症状之一,会显著影响生活质量。肺动脉高压患者运动不耐受的病理生理学很复杂,可能是多因素的。尽管右心室功能障碍以及灌注/通气不匹配的重要性已得到广泛认可,但最近的研究表明,骨骼肌的病理生理学也导致肺动脉高压患者运动能力下降,本文将探讨这一概念。