作为阻塞性睡眠呼吸暂停的P2X3受体对抗剂治疗的Gefapixant:一个随机对照试验
Jonathan A Robbins1, Scott Sands2, Lata Maganti1
1Merck & Co., Inc., Rahway, New Jersey.
概括
吉法皮克松 (Gefapixant) 并没有降低过敏化学反射患者的阻塞性睡眠呼吸暂停 (OSA) 严重程度. P2X3受体对手也增加了夜间低氧症,这表明它.
科学领域:
- 睡眠医学 睡眠医学
- 呼吸系统生理学 呼吸系统生理学
- 药理学 药理学是指药理学的学科.
背景情况:
- 阻塞性睡眠呼吸暂停 (OSA) 是一种普遍存在的疾病,治疗选择有限.
- 过敏化学反射控制呼吸是OSA患者的一个子集的关键机制.
- 目前,没有批准的治疗方法针对这种特定的内型特征.
研究的目的:
- 调查P2X3受体对抗剂fefapixant是否可以降低OSA的严重程度.
- 为了确定fefapixant是否减轻化学反射依赖于化学反射的OSA患者的过敏性心血管化学反射.
主要方法:
- 一项随机的,安慰剂控制的交叉研究,涉及24名中度至重度OSA患者.
- 患者在睡觉前口服Fefapixant 180 mg或安慰剂7天.
- 过夜的多睡眠记录被用来评估呼吸暂停-呼吸暂停指数 (AHI).
主要成果:
- 与安慰剂相比,格法皮克桑并没有显著降低AHI (比率0.92).
- 夜间低氧症在使用fefapixant时显著增加 (比率为2.08).
- 常见的不良事件包括味觉障碍和恶心.
结论:
- 格法皮克桑在降低化学反应依赖性OSA患者的OSA严重性的有效性没有被证明.
- P2X3受体对抗性不太可能成为OSA的可行的治疗策略.
- 格法皮克桑 (Gefapixant) 一般耐受良好,但对OSA严重程度没有提供临床益处.
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