抗抑郁药反应算法的跨电子病历验证以及与精神病特征遗传学的联系

Julia Sealock, Justin D Tubbs, Allison M Lake, Peter Straub, Jordan W. Smoller, Lea K. Davis
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引用次数: 0

摘要

目的:抗抑郁药是美国的常用处方药,但人们对其潜在的反应因素知之甚少。电子健康记录(EHR)为在大型纵向队列中创建和测试反应算法提供了一种经济有效的方法。我们介绍了一种新的抗抑郁药反应算法、在两个独立的电子病历数据库中进行的验证以及与抗抑郁药反应的遗传关联。方法:我们在范德比尔特大学医学中心(VUMC)、"我们所有人 "研究项目和麻省总布里格姆医疗保健系统(MGB)的电子病历中部署了该算法,并通过患者健康问卷(PHQ)得分验证了反应结果。在对所有研究机构进行的荟萃分析中,抗抑郁药反应较差与 PHQ-8 评分较高有关(β = 0.20,P 值 = 1.09 x 10-18)。结果我们使用多基因评分来研究 VUMC 和 MGB 的精神疾病遗传责任与首次抗抑郁试验反应之间的关系。在控制抑郁症诊断后,抑郁症、精神分裂症、双相情感障碍和交叉障碍的多基因评分越高,对首次抗抑郁试验的反应越差(抑郁症:p 值 = 2.84 x 10-8,OR = 1.07;精神分裂症:p 值 = 5.93 x 10-4,OR = 1.05;双相情感障碍:p 值 = 1.99 x 10-3,OR = 1.04;交叉障碍:p 值 = 1.03 x 10-3,OR = 1.05)。结论总之,我们证明了我们的抗抑郁反应算法可以在多个电子病历系统中使用,以增加抗抑郁反应遗传学和流行病学研究的样本量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cross-EHR validation of antidepressant response algorithm and links with genetics of psychiatric traits
Objective: Antidepressants are commonly prescribed medications in the United States, however, factors underlying response are poorly understood. Electronic health records (EHRs) provide a cost-effective way to create and test response algorithms on large, longitudinal cohorts. We describe a new antidepressant response algorithm, validation in two independent EHR databases, and genetic associations with antidepressant response. Method: We deployed the algorithm in EHRs at Vanderbilt University Medical Center (VUMC), the All of Us Research Program, and the Mass General Brigham Healthcare System (MGB) and validated response outcomes with patient health questionnaire (PHQ) scores. In a meta-analysis across all sites, worse antidepressant response associated with higher PHQ-8 scores (beta = 0.20, p-value = 1.09 x 10-18). Results: We used polygenic scores to investigate the relationship between genetic liability of psychiatric disorders and response to first antidepressant trial across VUMC and MGB. After controlling for depression diagnosis, higher polygenic scores for depression, schizophrenia, bipolar, and cross-disorders associated with poorer response to the first antidepressant trial (depression: p-value = 2.84 x 10-8, OR = 1.07; schizophrenia: p-value = 5.93 x 10-4, OR = 1.05; bipolar: p-value = 1.99 x 10-3, OR = 1.04; cross-disorders: p-value = 1.03 x 10-3, OR = 1.05). Conclusions: Overall, we demonstrate our antidepressant response algorithm can be deployed across multiple EHR systems to increase sample size of genetic and epidemiologic studies of antidepressant response.
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