Zhu Anqi, Zeng Donglin, Shen Li, Ning Xia, Li Lang, Zhang Pengyue
Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, Pennsylvania.
Stat Med. 2020 May 15;39(10):1458-1472. doi: 10.1002/sim.8490. Epub 2020 Feb 26.
Pharmacoinformatics research has experienced a great deal of successes in detecting drug-induced adverse events (AEs) using large-scale health record databases. In the era of polypharmacy, pharmacoinformatics faces many new challenges, and two significant challenges are to detect high-order drug interactions and to handle strongly correlated drugs. In this article, we propose a super-combo-drug test (SupCD-T) to address the aforementioned two challenges. SupCD-T detects drug interactions by identifying optimal drug combinations with increased AE risks. In addition, SupCD-T increases the statistical powers to detect single-drug effects by combining strongly correlated drugs. Although SupCD-T does not distinguish single-drug effects from their combination effects, it is noticeably more powerful in selecting an individual drug effect in the multiple regression analysis, where confounding justification between two correlated drugs reduces the power in testing the individual drug effects on AEs. Our simulation studies demonstrate that SupCD-T has generally better power comparing with the multiple regression analysis. In addition, SupCD-T is able to select meaningful drug combinations (eg, highly coprescribed drugs). Using electronic health record database, we illustrate the utility of SupCD-T and discover a number of drug combinations that have increased risk in myopathy. Some novel drug combinations have not yet been investigated and reported in the pharmacology research.
药物信息学研究在利用大规模健康记录数据库检测药物引起的不良事件(AE)方面取得了诸多成功。在联合用药的时代,药物信息学面临许多新挑战,其中两个重大挑战是检测高阶药物相互作用以及处理强相关药物。在本文中,我们提出了一种超级联合药物检验(SupCD-T)来应对上述两个挑战。SupCD-T通过识别具有增加的AE风险的最佳药物组合来检测药物相互作用。此外,SupCD-T通过合并强相关药物来提高检测单药效应的统计功效。尽管SupCD-T不能区分单药效应与其组合效应,但在多元回归分析中选择个体药物效应时,它明显更具功效,因为两种相关药物之间的混杂因素会降低检测单药对AE影响的功效。我们的模拟研究表明,与多元回归分析相比,SupCD-T通常具有更好的功效。此外,SupCD-T能够选择有意义的药物组合(例如,高共开处方药物)。利用电子健康记录数据库,我们展示了SupCD-T的效用,并发现了一些在肌病方面风险增加的药物组合。一些新型药物组合尚未在药理学研究中得到研究和报道。