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Respiratory and Limb Muscle Dysfunction in Pulmonary Arterial Hypertension: A Role for Exercise Training?:

机译:肺动脉高压中的呼吸和肢体肌肉功能障碍:运动训练的作用?:

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Respiratory and limb muscle dysfunction is emerging as an important pathophysiological abnormality in pulmonary arterial hypertension (PAH). Muscle abnormalities appear to occur frequently and promote dyspnea, fatigue, and exercise limitation in patients with PAH. Preliminary data suggest that targeted muscle training may be of benefit, although further evidence is required to consolidate these findings into specific recommendations for exercise training in patients with PAH. This article reviews the current evidence on prevalence, risk factors, and implications of respiratory and limb muscle dysfunction in patients with PAH. It also reviews the impact of exercise rehabilitation on morphologic, metabolic, and functional muscle profile and outcomes in PAH. Future research priorities are highlighted.
机译:呼吸和四肢肌肉功能障碍正在成为肺动脉高压(PAH)的重要病理生理异常。肌肉异常似乎经常发生,并会加剧PAH患者的呼吸困难,疲劳和运动受限。初步数据表明,有针对性的肌肉训练可能会有所帮助,尽管还需要进一步的证据来将这些发现整合为针对PAH患者进行运动训练的具体建议。本文回顾了有关PAH患者患病率,危险因素以及呼吸和肢体肌肉功能障碍的影响的最新证据。它还回顾了运动康复对PAH的形态,代谢和功能性肌肉状况及结局的影响。突出了未来的研究重点。

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