Horner Richard L, Grace Kevin P, Wellman Andrew
Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Department of Physiology, University of Toronto, Toronto, Ontario, Canada.
Respirology. 2017 Jul;22(5):861-873. doi: 10.1111/resp.13079. Epub 2017 May 25.
There is currently no pharmacotherapy for obstructive sleep apnoea (OSA) but there is no principled a priori reason why there should not be one. This review identifies a rational decision-making strategy with the necessary logical underpinnings that any reasonable approach would be expected to navigate to develop a viable pharmacotherapy for OSA. The process first involves phenotyping an individual to quantify and characterize the critical predisposing factor(s) to their OSA pathogenesis and identify, a priori, if the patient is likely to benefit from a pharmacotherapy that targets those factors. We then identify rational strategies to manipulate those critical predisposing factor(s), and the barriers that have to be overcome for success of any OSA pharmacotherapy. A new analysis then identifies candidate drug targets to manipulate the upper airway motor circuitry for OSA pharmacotherapy. The first conclusion is that there are two general pharmacological approaches for OSA treatment that are of the most potential benefit and are practically realistic, one being fairly intuitive but the second perhaps less so. The second conclusion is that after identifying the critical physiological obstacles to OSA pharmacotherapy, there are current therapeutic targets of high interest for future development. The final analysis provides a tabulated resource of 'druggable' targets that are relatively restricted to the circuitry controlling the upper airway musculature, with these candidate targets being of high priority for screening and further study. We also emphasize that a pharmacotherapy may not cure OSA per se, but may still be a useful adjunct to improve the effectiveness of, and adherence to, other treatment mainstays.
目前尚无针对阻塞性睡眠呼吸暂停(OSA)的药物疗法,但从原则上讲,没有理由不存在这样一种疗法。本综述确定了一种合理的决策策略,该策略具备必要的逻辑基础,任何合理的方法都有望借此开发出一种可行的OSA药物疗法。该过程首先涉及对个体进行表型分析,以量化和表征其OSA发病机制的关键易感因素,并预先确定患者是否可能从针对这些因素的药物疗法中获益。然后,我们确定操纵这些关键易感因素的合理策略,以及OSA药物疗法成功必须克服的障碍。一项新的分析随后确定了用于OSA药物疗法的操纵上气道运动回路的候选药物靶点。第一个结论是,有两种对OSA治疗最具潜在益处且切实可行的一般药理学方法,一种相当直观,另一种可能不那么直观。第二个结论是,在确定了OSA药物疗法的关键生理障碍后,目前有一些备受关注的未来治疗靶点。最后的分析提供了一个列表资源,列出了相对局限于控制上气道肌肉组织回路的“可药物化”靶点,这些候选靶点是筛选和进一步研究的高度优先对象。我们还强调,药物疗法本身可能无法治愈OSA,但仍可能是提高其他主要治疗方法的有效性和依从性的有用辅助手段。