Petkova Eva, Ogden R Todd, Tarpey Thaddeus, Ciarleglio Adam, Jiang Bei, Su Zhe, Carmody Thomas, Adams Philip, Kraemer Helena C, Grannemann Bruce D, Oquendo Maria A, Parsey Ramin, Weissman Myrna, McGrath Patrick J, Fava Maurizio, Trivedi Madhukar H
New York University, New York and Nathan Kline Institute for Psychiatric Research, Orangeburg, NY, USA.
Columbia University, New York, NY, USA.
Contemp Clin Trials Commun. 2017 Jun;6:22-30. doi: 10.1016/j.conctc.2017.02.007. Epub 2017 Feb 24.
Antidepressant medications are commonly used to treat depression, but only about 30% of patients reach remission with any single first-step antidepressant. If the first-step treatment fails, response and remission rates at subsequent steps are even more limited. The literature on biomarkers for treatment response is largely based on secondary analyses of studies designed to answer primary questions of efficacy, rather than on a planned systematic evaluation of biomarkers for treatment decision. The lack of evidence-based knowledge to guide treatment decisions for patients with depression has lead to the recognition that specially designed studies with the primary objective being to discover biosignatures for optimizing treatment decisions are necessary. Establishing Moderators and Biosignatures of Antidepressant Response in Clinical Care (EMBARC) is one such discovery study. Stage 1 of EMBARC is a randomized placebo controlled clinical trial of 8 week duration. A wide array of patient characteristics is collected at baseline, including assessments of brain structure, function and connectivity along with electrophysiological, biological, behavioral and clinical features. This paper reports on the data analytic strategy for discovering biosignatures for treatment response based on Stage 1 of EMBARC.
抗抑郁药物常用于治疗抑郁症,但任何一种单一的一线抗抑郁药物治疗后,只有约30%的患者达到缓解状态。如果第一步治疗失败,后续步骤的有效率和缓解率会更低。关于治疗反应生物标志物的文献主要基于旨在回答疗效主要问题的研究的二次分析,而不是基于对用于治疗决策的生物标志物的有计划的系统评估。缺乏基于证据的知识来指导抑郁症患者的治疗决策,已促使人们认识到有必要开展专门设计的研究,其主要目标是发现生物特征以优化治疗决策。“临床护理中抗抑郁反应的调节因素和生物特征”(EMBARC)研究就是这样一项探索性研究。EMBARC的第一阶段是一项为期8周的随机安慰剂对照临床试验。在基线时收集了广泛的患者特征,包括脑结构、功能和连通性评估以及电生理、生物学、行为和临床特征。本文报告了基于EMBARC第一阶段发现治疗反应生物特征的数据分析策略。