| Literature DB >> 28745547 |
Elodie Gautier-Veyret1,2,3, Sebastien Bailly2,3, Xavier Fonrose1, Julia Tonini1, Simon Chevalier1, Anne Thiebaut-Bertrand1,4, Françoise Stanke-Labesque1,2,3.
Abstract
How pharmacogenetics modulates the inhibitory effects of inflammation on voriconazole trough concentration (Cmin) remains unknown. In 29 recipients of allogeneic hematopoietic stem cell transplantation retrospectively studied, both a genetic score (which aggregated CYP2C19 and CYP3A genotypes) and inflammation significantly influenced voriconazole Cmin (n = 260). A trend toward (p = 0.03) a greater impact of inflammation in patients with the highest genetic score (corresponding to ultra-rapid metabolizers) was observed. Further researches are needed to confirm these data.Entities:
Keywords: CYP2C19; CYP3A4; inflammation; pharmacogenetics; therapeutic drug monitoring; voriconazole
Mesh:
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Year: 2017 PMID: 28745547 DOI: 10.2217/pgs-2017-0054
Source DB: PubMed Journal: Pharmacogenomics ISSN: 1462-2416 Impact factor: 2.533