Ticagrelor Increases Exposure to the Breast Cancer Resistance Protein Substrate Rosuvastatin
Publiceringsår
2023
Upphovspersoner
Lehtisalo, Minna; Tarkiainen, E. Katriina; Neuvonen, Mikko; Holmberg, Mikko; Kiiski, Johanna I.; Lapatto-Reiniluoto, Outi; Filppula, Anne M.; Kurkela, Mika; Backman, Janne T.; Niemi, Mikko
Abstrakt
<p>Ticagrelor and rosuvastatin are often used concomitantly after atherothrombotic events. Several cases of rhabdomyolysis during concomitant ticagrelor and rosuvastatin have been reported, suggesting a drug-drug interaction. We showed recently that ticagrelor inhibits breast cancer resistance protein (BCRP) and organic anion transporting polypeptide (OATP) 1B1, 1B3, and 2B1-mediated rosuvastatin transport in vitro. The aim of this study was to investigate the effects of ticagrelor on rosuvastatin pharmacokinetics in humans. In a randomized, crossover study, 9 healthy volunteers ingested a single dose of 90 mg ticagrelor or placebo, followed by a single 10 mg dose of rosuvastatin 1 hour later. Ticagrelor 90 mg or placebo were additionally administered 12, 24, and 36 hours after their first dose. Ticagrelor increased rosuvastatin area under the plasma concentration-time curve (AUC) and peak plasma concentration 2.6-fold (90% confidence intervals: 1.8-3.8 and 1.7-4.0, P = 0.001 and P = 0.003), and prolonged its half-life from 3.1 to 6.6 hours (P = 0.009). Ticagrelor also decreased the renal clearance of rosuvastatin by 11% (3%-19%, P = 0.032). The N-desmethylrosuvastatin:rosuvastatin AUC0-10h ratio remained unaffected by ticagrelor. Ticagrelor had no effect on the plasma concentrations of the endogenous OATP1B substrates glycodeoxycholate 3-O-glucuronide, glycochenodeoxycholate 3-O-glucuronide, glycodeoxycholate 3-O-sulfate, and glycochenodeoxycholate 3-O-sulfate, or the sodium-taurocholate cotransporting polypeptide substrate taurocholic acid. These data indicate that ticagrelor increases rosuvastatin concentrations more than twofold in humans, probably mainly by inhibiting intestinal BCRP. Because the risk for rosuvastatin-induced myotoxicity increases along with rosuvastatin plasma concentrations, using ticagrelor concomitantly with high doses of rosuvastatin should be avoided.</p>
Visa merOrganisationer och upphovspersoner
Helsingfors universitet
Filppula Anne M.
Tarkiainen E. Katriina
Backman Janne T.
Kiiski Johanna I.
Kurkela Mika
Holmberg Mikko
Neuvonen Mikko
Niemi Mikko
Lehtisalo Minna
Lapatto-Reiniluoto Outi
Helsingfors universitetssjukhus
Filppula Anne M.
Tarkiainen E. Katriina
Backman Janne T.
Kiiski Johanna I.
Kurkela Mika
Holmberg Mikko
Neuvonen Mikko
Niemi Mikko
Lehtisalo Minna
Lapatto-Reiniluoto Outi
Publikationstyp
Publikationsform
Artikel
Moderpublikationens typ
Tidning
Artikelstyp
En originalartikel
Målgrupp
VetenskapligKollegialt utvärderad
Kollegialt utvärderadUKM:s publikationstyp
A1 Originalartikel i en vetenskaplig tidskriftPublikationskanalens uppgifter
Journal/Serie
Moderpublikationens namn
ISSN
Publikationsforum
Publikationsforumsnivå
3
Öppen tillgång
Öppen tillgänglighet i förläggarens tjänst
Ja
Öppen tillgång till publikationskanalen
Delvis öppen publikationskanal
Licens för förläggarens version
CC BY NC
Parallellsparad
Ja
Parallellagringens licens
CC BY NC
Övriga uppgifter
Vetenskapsområden
Farmaci; Biomedicinska vetenskaper
Nyckelord
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Publiceringsland
Förenta staterna (USA)
Förlagets internationalitet
Internationell
Språk
engelska
Internationell sampublikation
Nej
Sampublikation med ett företag
Nej
DOI
10.1002/cpt.3067
Publikationen ingår i undervisnings- och kulturministeriets datainsamling
Ja