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选择治疗少肌症的潜在药物干预措施。

Selecting Potential Pharmacological Interventions in Sarcopenia.

作者信息

Kilsby Amanda J, Sayer Avan A, Witham Miles D

机构信息

Department of Geriatric Medicine, North Tyneside General Hospital, Northumbria Healthcare Trust, Rake Lane, North Shields, NE29 8NH, UK.

Ageing Geriatrics and Epidemiology, Institute of Neuroscience and Institute for Ageing, Newcastle University, Newcastle upon Tyne, UK.

出版信息

Drugs Aging. 2017 Apr;34(4):233-240. doi: 10.1007/s40266-017-0444-z.

Abstract

Sarcopenia of age is prevalent and costly and proven pharmacological interventions are currently lacking. The pathophysiology of sarcopenia is incompletely understood but appears to involve multiple pathways, including inflammation, hormonal dysregulation, impaired regeneration, mitochondrial dysfunction and denervation. There are several ways in which we might select potential pharmacological interventions for testing in clinical trials. These include a 'bottom-up' approach using basic science to elucidate the molecular processes involved and identify potential targets from this knowledge-a strategy that has led to the development of myostatin inhibitors. A 'top-down' approach might use observational data to examine the association between physical function and use of certain medications, such as the association between angiotensin-converting enzyme inhibitors with slower decline in physical function. Once a pharmacological intervention has been proposed, efficacy must be demonstrated in this complex multi-morbid population. Both muscle mass and muscle function need to be measured as outcomes, but these outcomes require large sample sizes and sufficient follow-up to detect change. Biomarkers that can predict the response of sarcopenia to intervention after a short time would greatly assist our ability to select candidate interventions in short proof-of-concept trials. Further development of trial methods is required to accelerate progress in this important area of medicine for older people.

摘要

衰老性肌肉减少症普遍存在且代价高昂,目前尚缺乏经证实的药物干预措施。肌肉减少症的病理生理学尚未完全明了,但似乎涉及多种途径,包括炎症、激素失调、再生受损、线粒体功能障碍和神经支配缺失。我们可以通过几种方式来选择潜在的药物干预措施用于临床试验测试。这些方式包括采用基础科学的“自下而上”方法来阐明其中涉及的分子过程,并据此知识确定潜在靶点——这一策略已促成了肌肉生长抑制素抑制剂的研发。“自上而下”的方法可能会利用观察性数据来研究身体功能与某些药物使用之间的关联,比如血管紧张素转换酶抑制剂与身体功能下降较慢之间的关联。一旦提出了一种药物干预措施,就必须在这个复杂的多病共存人群中证明其疗效。肌肉质量和肌肉功能都需要作为结果进行测量,但这些结果需要大样本量和足够的随访时间才能检测到变化。能够在短时间内预测肌肉减少症对干预反应的生物标志物将极大地帮助我们在短期概念验证试验中选择候选干预措施的能力。需要进一步改进试验方法,以加快在这一针对老年人的重要医学领域的进展。

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