Johnston Jenessa N, Zarate Carlos A, Kvarta Mark D
Experimental Therapeutics and Pathophysiology Branch, National Institute of Mental Health, National Institutes of Health, 10 Center Drive, Bethesda, MD, 20892, USA.
Eur Arch Psychiatry Clin Neurosci. 2024 Jul 13. doi: 10.1007/s00406-024-01865-1.
The discovery of racemic (R, S)-ketamine as a rapid-acting antidepressant and the subsequent FDA approval of its (S)-enantiomer, esketamine, for treatment-resistant depression (TRD) are significant advances in the development of novel neuropsychiatric therapeutics. Esketamine is now recognized as a powerful tool for addressing persistent symptoms of TRD compared to traditional oral antidepressants. However, research on biomarkers associated with antidepressant response to esketamine has remained sparse and, to date, has been largely extrapolated from racemic ketamine studies. Genetic, proteomic, and metabolomic profiles suggest that inflammation and mitochondrial function may play a role in esketamine's antidepressant effects, though these preliminary results require verification. In addition, neuroimaging research has consistently implicated the prefrontal cortex, striatum, and anterior cingulate cortex in esketamine's effects. Esketamine also shows promise in perioperative settings for reducing depression and anxiety, and these effects appear to correlate with increased peripheral biomarkers such as brain-derived neurotrophic factor and serotonin. Further indications are likely to be identified with the continued repurposing of racemic ketamine, providing further opportunity for biomarker study and mechanistic understanding of therapeutic effects. Novel methodologies and well-designed biomarker-focused clinical research trials are needed to more clearly elucidate esketamine's therapeutic actions as well as biologically identify those most likely to benefit from this agent, allowing for the improved personalization of antidepressant treatment.
消旋(R,S)-氯胺酮作为一种速效抗抑郁药的发现,以及随后美国食品药品监督管理局(FDA)批准其(S)-对映体艾氯胺酮用于治疗抵抗性抑郁症(TRD),是新型神经精神治疗药物开发中的重大进展。与传统口服抗抑郁药相比,艾氯胺酮现在被认为是解决TRD持续症状的有力工具。然而,与艾氯胺酮抗抑郁反应相关的生物标志物研究仍然稀少,迄今为止,大多是从消旋氯胺酮研究中推断出来的。遗传、蛋白质组学和代谢组学分析表明,炎症和线粒体功能可能在艾氯胺酮的抗抑郁作用中发挥作用,尽管这些初步结果需要验证。此外,神经影像学研究一直表明前额叶皮质、纹状体和前扣带回皮质与艾氯胺酮的作用有关。艾氯胺酮在围手术期减轻抑郁和焦虑方面也显示出前景,这些作用似乎与外周生物标志物如脑源性神经营养因子和血清素的增加相关。随着消旋氯胺酮的持续重新利用,可能会发现更多适应症,为生物标志物研究和治疗效果的机制理解提供更多机会。需要新的方法和精心设计的以生物标志物为重点的临床研究试验,以更清楚地阐明艾氯胺酮的治疗作用,并从生物学上确定最可能从该药物中获益的人群,从而改善抗抑郁治疗的个性化。