Evidence map›Paper›PMID 38255266›Full record

ArticleBiomedicines2024

Assessment of Substrate Status of Drugs Metabolized by Polymorphic Cytochrome P450 (CYP) 2 Enzymes: An Analysis of a Large-Scale Dataset.

Jakob Sommer, Justyna Wozniak, Judith Schmitt, Jana Koch, Julia C Stingl, Katja S Just

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Article in Biomedicines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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0cells of the map it votes in
5citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jakob SommerInstitute of Clinical Pharmacology, University Hospital of RWTH Aachen, 52074 Aachen, Germany.ORCID 0009-0001-1582-2264
Justyna WozniakInstitute of Clinical Pharmacology, University Hospital of RWTH Aachen, 52074 Aachen, Germany.
Judith SchmittInstitute of Clinical Pharmacology, University Hospital of RWTH Aachen, 52074 Aachen, Germany.
Jana KochInstitute of Clinical Pharmacology, University Hospital of RWTH Aachen, 52074 Aachen, Germany.
Julia C StinglInstitute of Clinical Pharmacology, University Hospital of RWTH Aachen, 52074 Aachen, Germany.ORCID 0000-0002-1566-8156
Katja S JustInstitute of Clinical Pharmacology, University Hospital of RWTH Aachen, 52074 Aachen, Germany.ORCID 0000-0002-6782-8078

Funding

European Union 101057639Federal Ministry of Health ZMVI5-2514ATA004Interdisciplinary Centre for Clinical Research PTD 1-9
6 · The paper itself

Abstract

backgroundThe analysis of substrates of polymorphic cytochrome P450 (CYP) enzymes is important information to enable drug-drug interactions (DDIs) analysis and the relevance of pharmacogenetics in this context in large datasets. Our aim was to compare different approaches to assess the substrate properties of drugs for certain polymorphic CYP2 enzymes.

methodsA standardized manual method and an automatic method were developed and compared to assess the substrate properties for the metabolism of drugs by CYP2D6, 2C9, and 2C19. The automatic method used a matching approach to three freely available resources. We applied the manual and automatic methods to a large real-world dataset deriving from a prospective multicenter study collecting adverse drug reactions in emergency departments in Germany (ADRED).

resultsIn total, 23,878 medication entries relating to 895 different drugs were analyzed in the real-world dataset. The manual method was able to assess 12.2% (

conclusionA closer look at different classifications between methods revealed that both methods are prone to error in different ways. While the automated method excels in time efficiency, completeness, and actuality, the manual method might be better able to identify CYP2 substrates with clinical relevance.

Indexed as

CYP2cytochrome P450 enzymedatabasedrug–drug–gene interactiondrug–drug interactionpharmacogeneticspharmacogenomicssoftware solution

Identifiers

PMID38255266
PMCPMC10813138

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.