| Literature DB >> 32770672 |
John J Lima1, Cameron D Thomas2, Julia Barbarino3, Zeruesenay Desta4, Sara L Van Driest5, Nihal El Rouby2,6, Julie A Johnson2, Larisa H Cavallari2, Valentina Shakhnovich7,8,9, David L Thacker10,11, Stuart A Scott12,13, Matthias Schwab14,15,16, Chakradhara Rao S Uppugunduri17,18, Christine M Formea19, James P Franciosi20,21, Katrin Sangkuhl3, Andrea Gaedigk7, Teri E Klein3, Roseann S Gammal22,23, Takahisa Furuta24.
Abstract
Proton pump inhibitors (PPIs) are widely used for acid suppression in the treatment and prevention of many conditions, including gastroesophageal reflux disease, gastric and duodenal ulcers, erosive esophagitis, Helicobacter pylori infection, and pathological hypersecretory conditions. Most PPIs are metabolized primarily by cytochrome P450 2C19 (CYP2C19) into inactive metabolites, and CYP2C19 genotype has been linked to PPI exposure, efficacy, and adverse effects. We summarize the evidence from the literature and provide therapeutic recommendations for PPI prescribing based on CYP2C19 genotype (updates at www.cpicpgx.org). The potential benefits of using CYP2C19 genotype data to guide PPI therapy include (i) identifying patients with genotypes predictive of lower plasma exposure and prescribing them a higher dose that will increase the likelihood of efficacy, and (ii) identifying patients on chronic therapy with genotypes predictive of higher plasma exposure and prescribing them a decreased dose to minimize the risk of toxicity that is associated with long-term PPI use, particularly at higher plasma concentrations.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32770672 PMCID: PMC7868475 DOI: 10.1002/cpt.2015
Source DB: PubMed Journal: Clin Pharmacol Ther ISSN: 0009-9236 Impact factor: 6.903