Journal article
Metabolomic and Genome‐wide Association Studies Reveal Potential Endogenous Biomarkers for OATP1B1
Abstract
Transporter-mediated drug-drug interactions (DDIs) are a major cause of drug toxicities. Using published genome-wide association studies (GWAS) of the human metabolome, we identified 20 metabolites associated with genetic variants in organic anion transporter, OATP1B1 (P < 5 × 10-8 ). Of these, 12 metabolites were significantly higher in plasma samples from volunteers dosed with the OATP1B1 inhibitor, cyclosporine (CSA) vs. placebo (q-value < …
Authors
Yee S; Giacomini M; Hsueh C; Weitz D; Liang X; Goswami S; Kinchen J; Coelho A; Zur A; Mertsch K
Journal
Clinical Pharmacology & Therapeutics, Vol. 100, No. 5, pp. 524–536
Publisher
Wiley
Publication Date
November 2016
DOI
10.1002/cpt.434
ISSN
0009-9236
Fields of Research (FoR)
Medical Subject Headings (MeSH)
Bile Acids and SaltsBiomarkersCyclosporineDicarboxylic AcidsDrug InteractionsFatty AcidsGenome-Wide Association StudyHEK293 CellsHumansLiver-Specific Organic Anion Transporter 1MetabolomicsMyristatesOrganic Anion Transport Protein 1Organic Anion Transporters, Sodium-IndependentPalmitic AcidsPravastatin