Potential Impact of Pharmacogenomic Single Nucleotide Variants in a Rural Caucasian Population
- PMID: 36611001
- PMCID: PMC10539040
- DOI: 10.1093/jalm/jfac091
Potential Impact of Pharmacogenomic Single Nucleotide Variants in a Rural Caucasian Population
Abstract
Background: In the US adverse drug reactions (ADRs) are estimated to cause 100 000 fatalities and cost over $136 billion annually. A patient's genes play a significant role in their response to a drug. Pharmacogenomics aims to optimize drug choice and dose for individual patients by characterizing patients' pharmacologically relevant genes to identify variants of known impact.
Methods: DNA was extracted from randomly selected remnant whole blood samples from Caucasian patients with previously performed complete blood counts. Samples were genotyped by mass spectrometry using a customized pharmacogenomics panel. A third-party result interpretation service used genotypic results to predict likely individual responses to frequently prescribed drugs.
Results: Complete genotypic and phenotypic calls for all tested Cytochrome P450 isoenzymes and other genes were obtained from 152 DNA samples. Of these 152 unique genomic DNA samples, 140 had genetic variants suggesting dose adjustment for at least one drug. Cardiovascular and psychiatry drugs had the highest number of recommendations, which included United States Food and Drug Administration warnings for highly prescribed drugs metabolized by CYP2C19, CYP2C9, CYP2D6, HLA-A, and VKORC1.
Conclusions: Risk for each drug:gene pairing primarily depends upon the degree of predicted enzyme impairment or activation, width of the therapeutic window, and whether parent compound or metabolite is pharmacologically active. The resulting metabolic variations range from risk of toxicity to therapeutic failure. Pharmacogenomic profiling likely reduces ADR potential by allowing up front drug/dose selection to fit a patient's unique drug-response profile.
© American Association for Clinical Chemistry 2023. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Conflict of interest statement
Figures

References
-
- Tan Y, Hu Y, Liu X, Yin Z, Chen XW, Liu M. Improving drug safety: from adverse drug reaction knowledge discovery to clinical implementation. Methods 2016; 110:14–25. - PubMed
-
- US Food and Drug Administration. Table of pharmacogenetic associations, https://www.fda.gov/drugs/science-and-research-drugs/table-pharmacogenom... (Accessed September 2021).
-
- Katara P, Yadav A. Pharmacogenes (PGx-genes): current understanding and future directions. Gene 2019;718: 1440–50. - PubMed
-
- Zanger UM, Schwab M. Cytochrome P450 enzymes in drug metabolism: regulation of gene expression, enzyme activities, and impact of genetic variation. Pharmacol Ther 2013;138:103–41. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials