Cross-EHR validation of antidepressant response algorithm and links with genetics of psychiatric traits

Julia Sealock, Justin D Tubbs, Allison M Lake, Peter Straub, Jordan W. Smoller, Lea K. Davis
{"title":"Cross-EHR validation of antidepressant response algorithm and links with genetics of psychiatric traits","authors":"Julia Sealock, Justin D Tubbs, Allison M Lake, Peter Straub, Jordan W. Smoller, Lea K. Davis","doi":"10.1101/2024.09.11.24313478","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":501388,"journal":{"name":"medRxiv - Psychiatry and Clinical Psychology","volume":"25 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"medRxiv - Psychiatry and Clinical Psychology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.09.11.24313478","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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
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。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Socio-medical Factors Associated with Neurodevelopmental Disorders on the Kenyan Coast Relationship between blood-cerebrospinal fluid barrier integrity, cardiometabolic and inflammatory factors in schizophrenia-spectrum disorders Whole-exome sequencing study of opioid dependence offers novel insights into the contributions of exome variants Mayo Normative Studies: regression-based normative data for remote self-administration of the Stricker Learning Span, Symbols Test and Mayo Test Drive Screening Battery Composite and validation in individuals with Mild Cognitive Impairment and dementia EEG frontal alpha asymmetry mediates the association between maternal and child internalizing symptoms in childhood
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1