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评估药物基因组学指导下的重度抑郁症治疗效果:快速回顾与荟萃分析。

Evaluating treatment outcomes in pharmacogenomic-guided care for major depression: A rapid review and meta-analysis.

作者信息

Bunka Mary, Wong Gavin, Kim Dan, Edwards Louisa, Austin Jehannine, Doyle-Waters Mary M, Gaedigk Andrea, Bryan Stirling

机构信息

School of Population and Public Health, University of British Columbia (UBC), 828 West 10th Avenue, Research Pavilion, 7th Floor, Vancouver, BC V5Z 1M9, Canada; Centre for Clinical Epidemiology and Evaluation, Vancouver Coastal Health Research Institute, Vancouver, BC, Canada.

School of Population and Public Health, University of British Columbia (UBC), 828 West 10th Avenue, Research Pavilion, 7th Floor, Vancouver, BC V5Z 1M9, Canada; Centre for Clinical Epidemiology and Evaluation, Vancouver Coastal Health Research Institute, Vancouver, BC, Canada.

出版信息

Psychiatry Res. 2023 Mar;321:115102. doi: 10.1016/j.psychres.2023.115102. Epub 2023 Feb 8.

Abstract

Pharmacogenomic (PGx) testing may increase the probability of remission and response in patients with major depressive disorder (MDD) undergoing pharmacotherapy. Given the potential implications of these outcomes and recent proliferation of PGx studies, we conducted a systematic review to evaluate the effectiveness of PGx testing on clinical outcomes in patients with MDD as compared to treatment as usual (TAU). MEDLINE, Embase, PsycInfo, and CENTRAL were searched for English-language articles from 2000 to 2021 for randomized controlled trials (RCTs) comparing PGx-guided treatment vs. TAU in patients with MDD. Meta-analyses were conducted in R. Ten RCTs were included: eight reported remission and seven reported response. The best available evidence suggests that PGx-guided care for moderate-to-severe adult depression is more likely to result in remission and response than TAU (both risk ratios significant). However, there are limitations in the evidence base, including high risk of bias and inconsistency between trials. Despite the consequent very low certainty in the magnitude of effect, there is confidence in the direction. Though modest, the beneficial effects of PGx for adults with moderate-severe MDD could - as a result of the scope and scale of the condition and its impacts - have important ramifications for patients and the health system.

摘要

药物基因组学(PGx)检测可能会提高接受药物治疗的重度抑郁症(MDD)患者缓解和产生反应的概率。鉴于这些结果的潜在影响以及PGx研究的近期激增,我们进行了一项系统评价,以评估与常规治疗(TAU)相比,PGx检测对MDD患者临床结局的有效性。检索了MEDLINE、Embase、PsycInfo和CENTRAL数据库,查找2000年至2021年期间比较PGx指导治疗与TAU对MDD患者疗效的英文随机对照试验(RCT)。在R软件中进行荟萃分析。纳入了10项RCT:8项报告了缓解情况,7项报告了反应情况。现有最佳证据表明,对于中重度成人抑郁症,PGx指导的治疗比TAU更有可能导致缓解和产生反应(风险比均具有统计学意义)。然而,证据基础存在局限性,包括偏倚风险高和各试验之间的不一致性。尽管因此对效应大小的确定性非常低,但对效应方向有信心。尽管PGx对中重度MDD成人的有益作用不大,但鉴于该疾病的范围和规模及其影响,可能会对患者和卫生系统产生重要影响。

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