Expert Opin Emerg Drugs. 2012 Sep;17(3):295-8. doi: 10.1517/14728214.2012.693158.
In recent years, there has been no evidence that the problem of chronic insomnia has faded in the least in US adults; on the contrary, a recent estimate of annual lost productivity due to insomnia was $63.2 billion dollars. However, the proportion of insomniacs who are treated continues to be low, indicating the need for continued development and dissemination of effective therapies. Hypnotic drug development has arguably become more focused in recent years, particularly upon the highly anticipated novel target, the orexin (hypocretin) system. Merck's suvorexant (MK-4305) is the first compound of the so-called dual orexin receptor antagonist (DORA) class expected to be submitted for FDA approval, with a new drug application anticipated in 2012. While there has also been some new activity in the modulation of well-characterized targets with well-characterized agents, such as CNS histamine receptors with low-dose doxepin, a decades-old antidepressant and GABA(A) with sublingual zolpidem, experience with melatonin and serotonin modulators suggests that other targets also exist. Diversifying insomnia drug targets may expand possibilities for customizing hypnotic administration to individualized patient presentation and mechanistic underpinnings. In addition, it may offer improved avenues for combining medications with non-drug treatments such as cognitive behavioral therapy for insomnia (CBT-I).
近年来,没有证据表明美国成年人的慢性失眠问题有丝毫减轻;相反,最近估计由于失眠导致的年生产力损失为 632 亿美元。然而,接受治疗的失眠症患者比例仍然很低,这表明需要继续开发和推广有效的治疗方法。近年来,催眠药物的开发无疑更加集中,特别是备受期待的新型靶点——食欲素(下丘脑分泌素)系统。默克公司的苏沃雷生(MK-4305)是首个所谓的双重食欲素受体拮抗剂(DORA)类化合物,预计将提交 FDA 批准,新药申请预计在 2012 年。虽然在使用具有明确作用机制的已知靶点调节方面也有一些新的进展,例如使用低剂量多塞平调节中枢组胺受体,或使用舌下唑吡坦调节 GABA(A)受体,但褪黑素和 5-羟色胺调节剂的经验表明,还存在其他靶点。使失眠药物靶点多样化可能为根据患者的具体表现和发病机制定制催眠药物的管理提供更多可能性。此外,它还可能为将药物与非药物治疗(如失眠认知行为疗法,CBT-I)相结合提供更好的途径。