Subset Analysis for Screening Drug–Drug Interaction Signal Using Pharmacovigilance Database

Many patients require multi-drug combinations, and adverse event profiles reflect not only the effects of individual drugs but also drug–drug interactions. Although there are several algorithms for detecting drug–drug interaction signals, a simple analysis model is required for early detection of ad...

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Main Authors: Yoshihiro Noguchi, Tomoya Tachi, Hitomi Teramachi
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/12/8/762
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spelling doaj-cc472d114efd44fcbae54c360e3a5af82020-11-25T03:46:39ZengMDPI AGPharmaceutics1999-49232020-08-011276276210.3390/pharmaceutics12080762Subset Analysis for Screening Drug–Drug Interaction Signal Using Pharmacovigilance DatabaseYoshihiro Noguchi0Tomoya Tachi1Hitomi Teramachi2Laboratory of Clinical Pharmacy, Gifu Pharmaceutical University, 1-25-4, Daigakunishi, Gifu-shi, Gifu 501-1196, JapanLaboratory of Clinical Pharmacy, Gifu Pharmaceutical University, 1-25-4, Daigakunishi, Gifu-shi, Gifu 501-1196, JapanLaboratory of Clinical Pharmacy, Gifu Pharmaceutical University, 1-25-4, Daigakunishi, Gifu-shi, Gifu 501-1196, JapanMany patients require multi-drug combinations, and adverse event profiles reflect not only the effects of individual drugs but also drug–drug interactions. Although there are several algorithms for detecting drug–drug interaction signals, a simple analysis model is required for early detection of adverse events. Recently, there have been reports of detecting signals of drug–drug interactions using subset analysis, but appropriate detection criterion may not have been used. In this study, we presented and verified an appropriate criterion. The data source used was the Japanese Adverse Drug Event Report (JADER) database; “hypothetical” true data were generated through a combination of signals detected by three detection algorithms. The accuracy of the signal detection of the analytic model under investigation was verified using indicators used in machine learning. The newly proposed subset analysis confirmed that the signal detection was improved, compared with signal detection in the previous subset analysis, on the basis of the indicators of <i>Accuracy</i> (0.584 to 0.809), <i>Precision</i> (= <i>Positive predictive value</i>; <i>PPV</i>) (0.302 to 0.596), <i>Specificity</i> (0.583 to 0.878), <i>Youden’s index</i> (0.170 to 0.465), <i>F</i>-<i>measure</i> (0.399 to 0.592), and <i>Negative predictive value</i> (<i>NPV</i>) (0.821 to 0.874). The previous subset analysis detected many false drug–drug interaction signals. Although the newly proposed subset analysis provides slightly lower detection accuracy for drug–drug interaction signals compared to signals compared to the Ω shrinkage measure model, the criteria used in the newly subset analysis significantly reduced the amount of falsely detected signals found in the previous subset analysis.https://www.mdpi.com/1999-4923/12/8/762subset analysissignal detection algorithmsdrug-drug interactionspontaneous reporting systems
collection DOAJ
language English
format Article
sources DOAJ
author Yoshihiro Noguchi
Tomoya Tachi
Hitomi Teramachi
spellingShingle Yoshihiro Noguchi
Tomoya Tachi
Hitomi Teramachi
Subset Analysis for Screening Drug–Drug Interaction Signal Using Pharmacovigilance Database
Pharmaceutics
subset analysis
signal detection algorithms
drug-drug interaction
spontaneous reporting systems
author_facet Yoshihiro Noguchi
Tomoya Tachi
Hitomi Teramachi
author_sort Yoshihiro Noguchi
title Subset Analysis for Screening Drug–Drug Interaction Signal Using Pharmacovigilance Database
title_short Subset Analysis for Screening Drug–Drug Interaction Signal Using Pharmacovigilance Database
title_full Subset Analysis for Screening Drug–Drug Interaction Signal Using Pharmacovigilance Database
title_fullStr Subset Analysis for Screening Drug–Drug Interaction Signal Using Pharmacovigilance Database
title_full_unstemmed Subset Analysis for Screening Drug–Drug Interaction Signal Using Pharmacovigilance Database
title_sort subset analysis for screening drug–drug interaction signal using pharmacovigilance database
publisher MDPI AG
series Pharmaceutics
issn 1999-4923
publishDate 2020-08-01
description Many patients require multi-drug combinations, and adverse event profiles reflect not only the effects of individual drugs but also drug–drug interactions. Although there are several algorithms for detecting drug–drug interaction signals, a simple analysis model is required for early detection of adverse events. Recently, there have been reports of detecting signals of drug–drug interactions using subset analysis, but appropriate detection criterion may not have been used. In this study, we presented and verified an appropriate criterion. The data source used was the Japanese Adverse Drug Event Report (JADER) database; “hypothetical” true data were generated through a combination of signals detected by three detection algorithms. The accuracy of the signal detection of the analytic model under investigation was verified using indicators used in machine learning. The newly proposed subset analysis confirmed that the signal detection was improved, compared with signal detection in the previous subset analysis, on the basis of the indicators of <i>Accuracy</i> (0.584 to 0.809), <i>Precision</i> (= <i>Positive predictive value</i>; <i>PPV</i>) (0.302 to 0.596), <i>Specificity</i> (0.583 to 0.878), <i>Youden’s index</i> (0.170 to 0.465), <i>F</i>-<i>measure</i> (0.399 to 0.592), and <i>Negative predictive value</i> (<i>NPV</i>) (0.821 to 0.874). The previous subset analysis detected many false drug–drug interaction signals. Although the newly proposed subset analysis provides slightly lower detection accuracy for drug–drug interaction signals compared to signals compared to the Ω shrinkage measure model, the criteria used in the newly subset analysis significantly reduced the amount of falsely detected signals found in the previous subset analysis.
topic subset analysis
signal detection algorithms
drug-drug interaction
spontaneous reporting systems
url https://www.mdpi.com/1999-4923/12/8/762
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