Noguchi Yoshihiro, Yoshizawa Shunsuke, Aoyama Keisuke, Kubo Satoaki, Tachi Tomoya, Teramachi Hitomi
Laboratory of Clinical Pharmacy, Gifu Pharmaceutical University, 1-25-4, Daigakunishi, Gifu-shi 501-1196, Gifu, Japan.
Pharmaceutics. 2021 Sep 22;13(10):1531. doi: 10.3390/pharmaceutics13101531.
The reporting odds ratio (ROR) is easy to calculate, and there have been several examples of its use because of its potential to speed up the detection of drug-drug interaction signals by using the "upward variation of ROR score". However, since the validity of the detection method is unknown, this study followed previous studies to investigate the detection trend. The statistics models (the Ω shrinkage measure and the "upward variation of ROR score") were compared using the verification dataset created from the Japanese Adverse Drug Event Report database (JADER). The drugs registered as "suspect drugs" in the verification dataset were considered as the drugs to be investigated, and the target adverse event in this study was Stevens-Johnson syndrome (SJS), as in previous studies. Of 3924 pairs that reported SJS, the number of positive signals detected by the Ω shrinkage measure and the "upward variation of ROR score" (Model 1, the Susuta Model, and Model 2) was 712, 2112, 1758, and 637, respectively. Furthermore, 1239 positive signals were detected when the Haldane-Anscombe 1/2 correction was applied to Model 2, the statistical model that showed the most conservative detection trend. This result indicated the instability of the positive signal detected in Model 2. The ROR scores based on the frequency-based statistics are easily inflated; thus, the use of the "upward variation of ROR scores" to search for drug-drug interaction signals increases the likelihood of false-positive signal detection. Consequently, the active use of the "upward variation of ROR scores" is not recommended, despite the existence of the Ω shrinkage measure, which shows a conservative detection trend.
报告比值比(ROR)易于计算,并且由于其有可能通过使用“ROR评分的上升变化”来加速药物相互作用信号的检测,已经有多个使用它的例子。然而,由于检测方法的有效性未知,本研究沿用先前的研究来调查检测趋势。使用从日本药品不良事件报告数据库(JADER)创建的验证数据集比较了统计模型(Ω收缩量度和“ROR评分的上升变化”)。在验证数据集中注册为“可疑药物”的药物被视为待研究的药物,并且与先前的研究一样,本研究中的目标不良事件是史蒂文斯 - 约翰逊综合征(SJS)。在报告SJS的3924对药物中,通过Ω收缩量度和“ROR评分的上升变化”(模型1、Susuta模型和模型2)检测到的阳性信号数量分别为712、2112、1758和637。此外,当对显示出最保守检测趋势的模型2应用霍尔丹 - 安斯康姆1/2校正时,检测到1239个阳性信号。这一结果表明在模型2中检测到的阳性信号不稳定。基于频率统计的ROR评分很容易被夸大;因此,使用“ROR评分的上升变化”来搜索药物相互作用信号会增加检测到假阳性信号的可能性。因此,尽管存在显示保守检测趋势的Ω收缩量度,但不建议积极使用“ROR评分的上升变化”。