Febuxostat, But Not Allopurinol, Markedly Raises the Plasma Concentrations of the Breast Cancer Resistance Protein Substrate Rosuvastatin

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Lehtisalo , M , Keskitalo , J E , Tornio , A , Lapatto-Reiniluoto , O , Deng , F , Jaatinen , T , Viinamäki , J , Neuvonen , M , Backman , J T & Niemi , M 2020 , ' Febuxostat, But Not Allopurinol, Markedly Raises the Plasma Concentrations of the Breast Cancer Resistance Protein Substrate Rosuvastatin ' , Clinical and translational science , vol. 13 , no. 6 , pp. 1236-1243 . https://doi.org/10.1111/cts.12809

Titel: Febuxostat, But Not Allopurinol, Markedly Raises the Plasma Concentrations of the Breast Cancer Resistance Protein Substrate Rosuvastatin
Författare: Lehtisalo, Minna; Keskitalo, Jenni E.; Tornio, Aleksi; Lapatto-Reiniluoto, Outi; Deng, Feng; Jaatinen, Taina; Viinamäki, Jenni; Neuvonen, Mikko; Backman, Janne T.; Niemi, Mikko
Upphovmannens organisation: INDIVIDRUG - Individualized Drug Therapy
Department of Clinical Pharmacology
Research Programs Unit
University of Helsinki
Helsinki University Hospital Area
HUSLAB
Janne Backman / Principal Investigator
Clinicum
Datum: 2020-11
Språk: eng
Sidantal: 8
Tillhör serie: Clinical and translational science
ISSN: 1752-8054
DOI: https://doi.org/10.1111/cts.12809
Permanenta länken (URI): http://hdl.handle.net/10138/325866
Abstrakt: Xanthine oxidase inhibitors febuxostat and allopurinol are commonly used in the treatment of gout. Febuxostat inhibits the breast cancer resistance protein (BCRP) in vitro. Rosuvastatin is a BCRP substrate and genetic variability in BCRP markedly affects rosuvastatin pharmacokinetics. In this study, we investigated possible effects of febuxostat and allopurinol on rosuvastatin pharmacokinetics. In a randomized crossover study with 3 phases, 10 healthy volunteers ingested once daily placebo for 7 days, 300 mg allopurinol for 7 days, or placebo for 3 days, followed by 120 mg febuxostat for 4 days, and a single 10 mg dose of rosuvastatin on day 6. Febuxostat increased the peak plasma concentration and area under the plasma concentration-time curve of rosuvastatin 2.1-fold (90% confidence interval 1.8-2.6; P = 5 x 10(-5)) and 1.9-fold (1.5-2.5; P = 0.001), but had no effect on rosuvastatin half-life or renal clearance. Allopurinol, on the other hand, did not affect rosuvastatin pharmacokinetics. In vitro, febuxostat inhibited the ATP-dependent uptake of rosuvastatin into BCRP-overexpressing membrane vesicles with a half-maximal inhibitory concentration of 0.35 mu M, whereas allopurinol showed no inhibition with concentrations up to 200 mu M. Taken together, the results suggest that febuxostat increases rosuvastatin exposure by inhibiting its BCRP-mediated efflux in the small intestine. Febuxostat may, therefore, serve as a useful index inhibitor of BCRP in drug-drug interaction studies in humans. Moreover, concomitant use of febuxostat may increase the exposure to BCRP substrate drugs and, thus, the risk of dose-dependent adverse effects.
Subject: DRUG-DRUG INTERACTION
HEPATIC-UPTAKE
ABCG2 BCRP
PHARMACOKINETICS
TRANSPORTER
GOUT
ELTROMBOPAG
OATP1B1
RISK
ATORVASTATIN
3111 Biomedicine
3121 General medicine, internal medicine and other clinical medicine
Referentgranskad: Ja
Licens: cc_by_nc
Användningsbegränsning: openAccess
Parallelpublicerad version: publishedVersion


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