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心力衰竭中的消瘦连续体:从肌肉减少症到恶病质。

The wasting continuum in heart failure: from sarcopenia to cachexia.

作者信息

von Haehling Stephan

机构信息

Department of Cardiology and Pneumology,University of Göttingen Medical School,Göttingen,Germany.

出版信息

Proc Nutr Soc. 2015 Nov;74(4):367-77. doi: 10.1017/S0029665115002438. Epub 2015 Aug 12.

Abstract

Sarcopenia (muscle wasting) and cachexia share some pathophysiological aspects. Sarcopenia affects approximately 20 %, cachexia <10 % of ambulatory patients with heart failure (HF). Whilst sarcopenia means loss of skeletal muscle mass and strength that predominantly affects postural rather than non-postural muscles, cachexia means loss of muscle and fat tissue that leads to weight loss. The wasting continuum in HF implies that skeletal muscle is lost earlier than fat tissue and may lead from sarcopenia to cachexia. Both tissues require conservation, and therapies that stop the wasting process have tremendous therapeutic appeal. The present paper reviews the pathophysiology of muscle and fat wasting in HF and discusses potential treatments, including exercise training, appetite stimulants, essential amino acids, growth hormone, testosterone, electrical muscle stimulation, ghrelin and its analogues, ghrelin receptor agonists and myostatin antibodies.

摘要

肌肉减少症(肌肉萎缩)和恶病质有一些共同的病理生理特征。肌肉减少症影响约20%的门诊心力衰竭(HF)患者,恶病质影响不到10%的门诊HF患者。肌肉减少症是指骨骼肌质量和力量的丧失,主要影响姿势肌而非非姿势肌,而恶病质是指肌肉和脂肪组织的丧失导致体重减轻。HF中的消瘦连续体意味着骨骼肌比脂肪组织更早丢失,可能从肌肉减少症发展为恶病质。这两种组织都需要保护,能够阻止消瘦过程的疗法具有巨大的治疗吸引力。本文综述了HF中肌肉和脂肪消瘦的病理生理学,并讨论了潜在的治疗方法,包括运动训练、食欲刺激剂、必需氨基酸、生长激素、睾酮、肌肉电刺激、胃饥饿素及其类似物、胃饥饿素受体激动剂和肌肉生长抑制素抗体。

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