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慢性心力衰竭中的骨骼肌耗损。

Skeletal muscle wasting in chronic heart failure.

机构信息

Department of Cardiology and Pneumology, University Medical Center Göttingen (UMG), Göttingen, Germany.

出版信息

ESC Heart Fail. 2018 Dec;5(6):1099-1107. doi: 10.1002/ehf2.12387. Epub 2018 Dec 7.

Abstract

Patients suffering from chronic heart failure (CHF) show an increased prevalence (~20% in elderly CHF patients) of loss of muscle mass and muscle function (i.e. sarcopenia) compared with healthy elderly people. Sarcopenia, which can also occur in obese patients, is considered a strong predictor of frailty, disability, and mortality in older persons and is present in 5-13% of elderly persons aged 60-70 years and up to 50% of all octogenarians. In a CHF study, sarcopenia was associated with lower strength, reduced peak oxygen consumption (peak VO , 1173 ± 433 vs. 1622 ± 456 mL/min), and lower exercise time (7.7 ± 3.8 vs. 10.22 ± 3.0 min, both P < 0.001). Unfortunately, there are only very limited therapy options. Currently, the main intervention remains resistance exercise. Specialized nutritional support may aid the effects of resistance training. Testosterone has significant positive effects on muscle mass and function, and low endogenous testosterone has been described as an independent risk factor in CHF in a study with 618 men (hazard ratio 0.929, P = 0.042). However, the use of testosterone is controversial because of possible side effects. Selective androgen receptor modulators have been developed to overcome these side effects but are not yet available on the market. Further investigational drugs include growth hormone, insulin-like growth factor 1, and several compounds that target the myostatin pathway. The continuing development of new treatment strategies and compounds for sarcopenia, muscle wasting regardless of CHF, and cardiac cachexia makes this a stimulating research area.

摘要

患有慢性心力衰竭 (CHF) 的患者与健康老年人相比,肌肉质量和肌肉功能(即肌少症)的丧失更为常见(老年 CHF 患者中约为 20%)。肌少症也可能发生在肥胖患者中,被认为是老年人虚弱、残疾和死亡的强有力预测指标,在 60-70 岁的老年人中占 5-13%,在所有 80 岁以上的老年人中占 50%。在一项 CHF 研究中,肌少症与较低的力量、较低的峰值耗氧量(peak VO₂,1173±433 与 1622±456 mL/min)和较短的运动时间(7.7±3.8 与 10.22±3.0 min,均 P<0.001)相关。不幸的是,目前仅有非常有限的治疗选择。目前,主要的干预措施仍然是阻力运动。专门的营养支持可能有助于抵抗训练的效果。睾丸酮对肌肉质量和功能有显著的积极影响,在一项纳入 618 名男性的研究中,低内源性睾丸酮被描述为 CHF 的独立危险因素(风险比 0.929,P=0.042)。然而,由于可能存在副作用,睾丸酮的使用存在争议。选择性雄激素受体调节剂的开发是为了克服这些副作用,但尚未在市场上使用。进一步的研究药物包括生长激素、胰岛素样生长因子 1 以及几种针对肌肉生长抑制素途径的化合物。新的治疗策略和化合物的不断发展,包括肌少症、与 CHF 无关的肌肉消耗和心脏恶病质,使这成为一个令人兴奋的研究领域。

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本文引用的文献

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Relation of Testosterone Levels to Mortality in Men With Heart Failure.睾酮水平与心力衰竭男性死亡率的关系。
Am J Cardiol. 2018 Jun 1;121(11):1321-1327. doi: 10.1016/j.amjcard.2018.01.052. Epub 2018 Mar 1.
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ESC Heart Fail. 2018 Apr;5(2):222-232. doi: 10.1002/ehf2.12225. Epub 2017 Dec 13.
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Skeletal muscle performance and ageing.骨骼肌性能与衰老。
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