The Potential Influence of Associated Antidepressants on the Pharmacokinetic Profile of Esketamine in Patients Affected by Treatment-resistant Depression.

IF 4.8 2区 医学 Q1 NEUROSCIENCES
Marika Alborghetti, Luana Lionetto, Ginevra Lombardozzi, Luca Montaguti, Giada Trovini, Daniela Donato, Giuseppe Costanzi, Donatella De Bernardini, Federica Catapano, Michele Surano, Ilaria Pagano, Alessia Ceccherelli, Edoardo Bianchini, Giorgio Di Lorenzo, Maurizio Simmaco, Giovanni Martinotti, Georgios D Kotzalidis, Ferdinando Nicoletti, Sergio De Filippis
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引用次数: 0

Abstract

Introduction/objective: Esketamine is administered intranasally in combination with at least another antidepressant in patients with treatment-resistant depression. Some of these antidepressants might affect ketamine's pharmacokinetic profile by inhibiting cytochrome-P450 (CYP450) isoforms. Our aim was to establish how different types of combined antidepressants affect serum and salivary levels of esketamine at the time of maximum plasma concentrations and afterward in TRD patients receiving esketamine in a real-world context.

Methods: Serum and salivary samples were collected from 53 patients receiving intranasal esketamine (56 mg) at baseline, after 20 min (roughly corresponding to Tmax), 7 hours (corresponding to the t½ value), 24, and 72 hours. Patients were stratified according to the combined antidepressant medication.

Results: Salivary esketamine levels were several-fold higher than the corresponding serum levels at all time points, and showed high inter-individual variability. Serum 20-min post-esketamine levels and AUC0-72 levels were significantly higher in patients on antidepressants known to inhibit different isoforms of CYP450 (paroxetine, fluoxetine, duloxetine, venlafaxine), with respect to levels detected in patients on sertraline, citalopram, escitalopram, vortioxetine. These changes in the pharmacokinetic profile of esketamine did not affect the clinical outcome of esketamine. However, changes in systolic blood pressure in response to esketamine positively correlated with serum esketamine levels, suggesting a reduction of esketamine dose in patients with cardiovascular comorbidity under treatment with paroxetine, fluoxetine, duloxetine, venlafaxine.

Conclusion: The CYP450-related status of co-administered antidepressants may affect esketamine levels. However, the small sample sizes of the co-administered drug subgroups and multiple prescriptions do not allow for drawing strong conclusions.

相关抗抑郁药对难治性抑郁症患者艾氯胺酮药代动力学的潜在影响
简介/目的:在难治性抑郁症患者中,艾氯胺酮与至少另一种抗抑郁药联合鼻内给药。其中一些抗抑郁药可能通过抑制细胞色素p450 (CYP450)异构体影响氯胺酮的药代动力学特征。我们的目的是确定不同类型的联合抗抑郁药如何影响在现实世界中接受艾氯胺酮治疗的TRD患者在最大血浆浓度时和之后的血清和唾液艾氯胺酮水平。方法:对53例接受鼻内埃氯胺酮(56 mg)治疗的患者,分别在基线、20min(大致对应Tmax)、7h(对应t1 / 2值)、24h和72h后采集血清和唾液样本。根据联合抗抑郁药物对患者进行分层。结果:各时间点唾液艾氯胺酮水平均高于相应血清水平数倍,且个体间差异较大。服用抗抑郁药物(帕罗西汀、氟西汀、度洛西汀、文拉法辛)的患者在服用艾氯胺酮20分钟后血清中CYP450不同亚型的水平和AUC0-72水平明显高于服用舍曲林、西酞普兰、艾司西酞普兰、沃替西汀的患者。艾氯胺酮的药代动力学特征的这些变化并不影响艾氯胺酮的临床结果。然而,对艾氯胺酮反应的收缩压变化与血清艾氯胺酮水平正相关,表明在帕罗西汀、氟西汀、度洛西汀、文拉法辛治疗的心血管合并症患者中,艾氯胺酮剂量减少。结论:合用抗抑郁药的cyp450相关状态可能影响艾氯胺酮水平。然而,联合用药亚组的小样本量和多个处方不能得出强有力的结论。
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来源期刊
Current Neuropharmacology
Current Neuropharmacology 医学-神经科学
CiteScore
8.70
自引率
1.90%
发文量
369
审稿时长
>12 weeks
期刊介绍: Current Neuropharmacology aims to provide current, comprehensive/mini reviews and guest edited issues of all areas of neuropharmacology and related matters of neuroscience. The reviews cover the fields of molecular, cellular, and systems/behavioural aspects of neuropharmacology and neuroscience. The journal serves as a comprehensive, multidisciplinary expert forum for neuropharmacologists and neuroscientists.
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