Bupropion-Memantine Combination in the Treatment of Major Depressive Disorder and Treatment-Resistant Depression

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY
Juan Miguel Riestra, Yaxel Levin-Carrion, Roshan Sutar, Jessica Mitchell, Pranav Jambulingam, Santiago J. Ballaz, Mujeeb U. Shad, Shafiqur Rahman, Stefano Barlati, Maju Mathew Koola
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引用次数: 0

Abstract

Treatment-resistant depression (TRD) remains a formidable challenge in psychiatry, with nearly one-third of patients with major depressive disorder (MDD) failing to respond adequately to first-line pharmacological treatments. Pathophysiology in MDD has highlighted the N-methyl-D-aspartate (NMDA) glutamatergic system as a promising therapeutic target. In 2022, the US Food and Drug Administration (FDA) approved the bupropion and dextromethorphan (DXM) combination (BDC), the first oral combination that affects both the NMDA receptor and norepinephrine-dopamine systems. DXM is an uncompetitive NMDA receptor antagonist, and in combination with bupropion, it has been shown to be a rapidly acting oral medication with clinically significant improvement in the first week of treatment. BDC, however, has many inherent limitations such as contraindications in those with eating disorders and a history of seizures. Anxiety is a common comorbidity in MDD, and bupropion has been shown to lack efficacy in treating anxiety. In addition, BDC did not improve cognition. Memantine can treat depression and cognitive impairments concurrently. Fixed-dose combination pills can be less flexible than prescribing each drug separately, as BDC is limited to a 105 mg (bupropion)-45 mg (DXM) combination. The projected 1-month cost of possible combinations of memantine ($5.00) with a selective serotonin reuptake inhibitor (SSRI, $4.00), serotonin-norepinephrine reuptake inhibitor (SNRI, $15.00), and bupropion ($18.00) are cheaper than BDC ($1119.00). Instead of BDC, we propose various alternatives such as a bupropion-memantine combination or SSRI/SNRI and memantine for MDD/TRD.

安非他酮-美金刚联合治疗重度抑郁症及难治性抑郁症。
难治性抑郁症(TRD)在精神病学中仍然是一个巨大的挑战,近三分之一的重度抑郁症(MDD)患者对一线药物治疗没有充分的反应。MDD的病理生理学强调n -甲基- d -天冬氨酸(NMDA)谷氨酸能系统是一个有希望的治疗靶点。2022年,美国食品和药物管理局(FDA)批准了安非他酮和右美沙芬(DXM)组合(BDC),这是第一个同时影响NMDA受体和去甲肾上腺素-多巴胺系统的口服组合。DXM是一种非竞争性NMDA受体拮抗剂,与安非他酮联合使用,已被证明是一种快速作用的口服药物,在治疗的第一周就有显著的临床改善。然而,BDC有许多固有的局限性,如饮食失调和癫痫史的禁忌。焦虑是重度抑郁症的常见合并症,而安非他酮在治疗焦虑方面缺乏疗效。此外,BDC并没有改善认知。美金刚可以同时治疗抑郁症和认知障碍。固定剂量的组合药片可能不如单独开具每种药物灵活,因为BDC被限制为105毫克(安非他酮)-45毫克(DXM)的组合。美金刚啶与选择性5 -羟色胺再摄取抑制剂(SSRI, 4.00美元)、5 -羟色胺-去甲肾上腺素再摄取抑制剂(SNRI, 15.00美元)和安非他酮(18.00美元)联合使用的预计1个月费用比BDC(1119.00美元)便宜。代替BDC,我们提出了各种替代方案,如安非他酮-美金刚联合或SSRI/SNRI和美金刚治疗MDD/TRD。
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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
34
审稿时长
6-12 weeks
期刊介绍: Human Psychopharmacology: Clinical and Experimental provides a forum for the evaluation of clinical and experimental research on both new and established psychotropic medicines. Experimental studies of other centrally active drugs, including herbal products, in clinical, social and psychological contexts, as well as clinical/scientific papers on drugs of abuse and drug dependency will also be considered. While the primary purpose of the Journal is to publish the results of clinical research, the results of animal studies relevant to human psychopharmacology are welcome. The following topics are of special interest to the editors and readers of the Journal: -All aspects of clinical psychopharmacology- Efficacy and safety studies of novel and standard psychotropic drugs- Studies of the adverse effects of psychotropic drugs- Effects of psychotropic drugs on normal physiological processes- Geriatric and paediatric psychopharmacology- Ethical and psychosocial aspects of drug use and misuse- Psychopharmacological aspects of sleep and chronobiology- Neuroimaging and psychoactive drugs- Phytopharmacology and psychoactive substances- Drug treatment of neurological disorders- Mechanisms of action of psychotropic drugs- Ethnopsychopharmacology- Pharmacogenetic aspects of mental illness and drug response- Psychometrics: psychopharmacological methods and experimental design
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