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在重度抑郁症中组合药物基因组学方法的临床验证:一项观察性前瞻性随机、参与者和评估者设盲、对照试验(PANDORA 试验)。

Clinical validation of a combinatorial PharmAcogeNomic approach in major Depressive disorder: an Observational prospective RAndomized, participant and rater-blinded, controlled trial (PANDORA trial).

机构信息

Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.

Genetics Unit, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Via Pilastroni, 4, 25125, Brescia, Italy.

出版信息

Trials. 2021 Dec 11;22(1):896. doi: 10.1186/s13063-021-05775-8.

Abstract

BACKGROUND

Major depressive disorder (MDD) is a common, chronic, debilitating mood disorder that causes serious functional impairment and significantly decreased quality of life. Pharmacotherapy represents the first-line treatment option; however, only approximately one third of patients respond to the first treatment because of the ineffectiveness or side effects of antidepressants. Precision medicine in psychiatry might offer clinicians the possibility to tailor treatment according to the best possible evidence of efficacy and tolerability for each subject. In this context, our study aims to carry out a clinical validation of a combinatorial pharmacogenomics (PGx) test in an Italian MDD patient cohort with advocacy license independence.

METHODS

Our study is a prospective participant- and rater-blinded, randomized, controlled clinical observational trial enrolling 300 MDD patients who are referred to psychiatric services to receive a new antidepressant due to the failure of their current treatment and/or the onset of adverse effects. Eligible participants are randomized to the TGTG group (Treated with Genetic Test Guide) or TAU group (Treated as Usual). For all subjects, DNA is collected with a buccal brush. The primary outcome is the reduction in depressive symptomatology. The secondary outcomes involve a range of scales that assess MDD symptoms and social functioning outcomes. The assessment is performed at four timepoints: baseline and 4, 8, and 12 weeks.

DISCUSSION

This project represents the first randomized controlled clinical trial to investigate whether a non-commercial PGx test improves outcomes in an MDD naturalistic cohort. Moreover, the identification of new genetic variants associated with non-response or side effects will improve the efficacy of the test, leading to further cost-saving.

TRIAL REGISTRATION NUMBER

ClinicalTrials.gov NCT04615234. Registered on November 4, 2020.

摘要

背景

重度抑郁症(MDD)是一种常见的、慢性的、使人虚弱的情绪障碍,它会导致严重的功能障碍和生活质量显著下降。药物治疗是首选治疗方案;然而,由于抗抑郁药的无效或副作用,只有约三分之一的患者对第一种治疗有反应。精神科的精准医学可能为临床医生提供根据每个患者的最佳疗效和耐受性证据来定制治疗的可能性。在这种情况下,我们的研究旨在对意大利 MDD 患者队列进行组合式药物遗传学(PGx)测试的临床验证,该测试具有独立的倡导许可证。

方法

我们的研究是一项前瞻性的参与者和评估者盲法、随机、对照的临床观察性试验,纳入了 300 名 MDD 患者,他们因当前治疗失败和/或出现不良反应而被转介到精神科服务机构接受新的抗抑郁药治疗。符合条件的参与者被随机分配到 TGTG 组(用遗传测试指南治疗)或 TAU 组(常规治疗)。所有受试者均使用口腔拭子采集 DNA。主要结局是抑郁症状的减轻。次要结局涉及一系列评估 MDD 症状和社会功能结局的量表。评估在四个时间点进行:基线和 4、8 和 12 周。

讨论

该项目是第一项调查非商业性 PGx 测试是否能改善 MDD 自然队列中结果的随机对照临床试验。此外,鉴定与无反应或副作用相关的新遗传变异将提高测试的疗效,从而进一步节省成本。

试验注册编号

ClinicalTrials.gov NCT04615234。于 2020 年 11 月 4 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d4a/8665483/86d970551724/13063_2021_5775_Fig1_HTML.jpg

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