Comparative efficacy of antidepressant augmentation with amantadine vs pramipexole in treatment-resistant unipolar depression: A randomised controlled trial.

IF 4.9 2区 医学 Q1 CLINICAL NEUROLOGY
Biswa Ranjan Mishra, Debadatta Mohapatra, Tathagata Biswas, Archana Mishra, Sahadeb Panigrahi, Rituparna Maiti
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引用次数: 0

Abstract

Background: Augmentation strategies for treatment-resistant depression (TRD) are limited, with strongest evidence for atypical antipsychotics. Given emerging insights into the neurobiology of TRD, new drug classes merit investigation. We hypothesised that augmentation with amantadine (NMDA antagonist) and pramipexole (dopamine agonist) would show comparable efficacy and safety to quetiapine in TRD.

Methods: In this open-label trial, 150 patients with TRD were equally randomised to receive amantadine 200 mg/day, pramipexole 37.5 mg/day, or quetiapine 100 mg/day, as augmentation to ongoing sertraline. The Hamilton Depression Rating Scale (HAM-D21) and Clinical Global Impression (CGI)-Severity and CGI-Improvement scales were assessed and compared within and between the groups at baseline, four, and eight weeks. Serum Brain-Derived Neurotrophic Factor (BDNF) and Nerve Growth Factor (NGF) were measured at baseline, four and eight weeks to evaluate and compare neurotrophic changes between the groups alongside clinical response.

Results: Mixed-model ANOVA revealed significant HAM-D and CGI-S reductions in all three groups over eight weeks (p < 0.001). Between-group analysis revealed pramipexole was significantly better compared to both amantadine and quetiapine on all clinical measures at weeks four and eight (p < 0.001). Amantadine and quetiapine showed comparable efficacy (p > 0.05). BDNF and NGF levels increased significantly within each group (p < 0.001), but between-group differences were non-significant (p > 0.05). The three groups reported similar occurence of adverse events (p = 0.184).

Conclusion: Augmentation with amantadine and pramipexole were safe and effective in TRD. Additionally, pramipexole showed better efficacy to amantadine and quetiapine. Clinical improvements corroborated with improved BDNF and NGF levels. However, larger multi-centric studies are warranted for generalisability. (ClinicalTrials.gov: NCT04936126).

金刚烷胺增强抗抑郁药与普拉克索治疗难治性单极抑郁症的比较疗效:一项随机对照试验。
背景:增强治疗难治性抑郁症(TRD)的策略是有限的,最有力的证据是非典型抗精神病药物。鉴于对TRD神经生物学的新见解,新的药物类别值得研究。我们假设金刚烷胺(NMDA拮抗剂)和普拉克索(多巴胺激动剂)对TRD的疗效和安全性与喹硫平相当。方法:在这项双盲试验中,150名TRD患者同样随机接受金刚烷胺200 mg/天,普拉克索37.5 mg/天或喹硫平100 mg/天,作为正在使用的舍曲林的补充。汉密尔顿抑郁评定量表(HAMD 21)和临床总体印象(CGI)-严重程度和CGI-改善量表在基线、4周和8周进行评估和组内和组间比较。在基线、4周和8周时测量血清脑源性神经营养因子(BDNF)和神经生长因子(NGF),以评估和比较各组之间的神经营养变化和临床反应。结果:混合模型方差分析显示,三组患者在8周内HAMD和CGI-S均显著降低(p  0.05)。各组BDNF、NGF水平均显著升高(p  0.05)。三组不良事件发生率相似(p = 0.184)。结论:金刚烷胺加普拉克索治疗TRD安全有效。普拉克索的疗效优于金刚烷胺和喹硫平。临床改善证实了BDNF和NGF水平的提高。然而,更大的多中心研究是必要的普遍性。(ClinicalTrials.gov: NCT04936126)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of affective disorders
Journal of affective disorders 医学-精神病学
CiteScore
10.90
自引率
6.10%
发文量
1319
审稿时长
9.3 weeks
期刊介绍: The Journal of Affective Disorders publishes papers concerned with affective disorders in the widest sense: depression, mania, mood spectrum, emotions and personality, anxiety and stress. It is interdisciplinary and aims to bring together different approaches for a diverse readership. Top quality papers will be accepted dealing with any aspect of affective disorders, including neuroimaging, cognitive neurosciences, genetics, molecular biology, experimental and clinical neurosciences, pharmacology, neuroimmunoendocrinology, intervention and treatment trials.
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