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A resource of potential drug targets and strategic decision-making for obstructive sleep apnoea pharmacotherapy

期刊

RESPIROLOGY
卷 22, 期 5, 页码 861-873

出版社

WILEY
DOI: 10.1111/resp.13079

关键词

neurobiology; obstructive sleep apnoea; phenotype; sleep; translational medical research

资金

  1. Canadian Institutes of Health Research (CIHR) [MT-15563]
  2. National Sanitarium Association Innovative Research Program [00144051]
  3. Tier I Canada Research Chair in Sleep and Respiratory Neurobiology [950-229813]
  4. CIHR Doctoral Award: Fredrick Banting and Charles Best Canada Graduate Scholarship (CGS-D)
  5. Sleep and Biological Rhythms Toronto-a CIHR Team Research and Program
  6. Queen Elizabeth II/Grace Lumsden/Margaret Nicholds Scholarship in Science and Technology (QEII-GSST)
  7. National Institutes of Health [R01 HL102321, R01 HL 128658, P01 HL 095491, P01 HL 094307]

向作者/读者索取更多资源

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 OSAper se, but may still be a useful adjunct to improve the effectiveness of, and adherence to, other treatment mainstays.

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