Roxadustat Does Not Affect Platelet Production, Activation, and Thrombosis Formation

Arterioscler Thromb Vasc Biol. 2021 Oct;41(10):2523-2537. doi: 10.1161/ATVBAHA.121.316495. Epub 2021 Aug 5.

Abstract

Objective: Roxadustat is a new medication for the treatment of renal anemia. EPO (erythropoietin)-the current treatment standard-has been reported to enhance platelet activation and production. However, to date, the effect of roxadustat on platelets is unclear. To address this deficiency, herein, we have evaluated the effect of roxadustat on platelet production and function. Approach and Results: We performed several mouse platelet functional assays in the presence/absence of in vitro and in vivo roxadustat treatment. Both healthy and 5/6 nephrectomized mice were utilized. The effect of roxadustat on platelet function of healthy volunteers and chronic kidney disease patients was also evaluated. For platelet production, megakaryocyte maturation and proplatelet formation were assayed in vitro. Peripheral platelet and bone marrow megakaryocyte counts were also determined. We found that roxadustat could not stimulate washed platelets directly, and platelet aggregation, spreading, clot retraction, and P-selectin/JON/A exposure were similar with or without in vitro or in vivo roxadustat treatment among both healthy and 5/6 nephrectomized mice. In vivo mouse thrombosis models were additionally performed, and no differences were detected between the vehicle and roxadustat treatment groups. EPO, which was considered a positive control in the present study, promoted platelet function and production as reported previously. Megakaryocyte maturation and proplatelet formation were also not significantly different between control mice and those treated with roxadustat. After receiving roxadustat for 14 days, no difference in the peripheral platelet count was observed in the mice. Conclusions: Administration of roxadustat has no significant impact on platelet production and function.

Keywords: blood platelets; platelet aggregation; platelet count; renal insufficiency, chronic; thrombosis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Coagulation / drug effects*
  • Blood Platelets / drug effects*
  • Blood Platelets / metabolism
  • Case-Control Studies
  • Disease Models, Animal
  • Erythropoietin / pharmacology*
  • Erythropoietin / toxicity
  • Glycine / analogs & derivatives*
  • Glycine / pharmacology
  • Glycine / toxicity
  • Hematinics / pharmacology*
  • Hematinics / toxicity
  • Humans
  • Isoquinolines / pharmacology*
  • Isoquinolines / toxicity
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Platelet Activation / drug effects*
  • Renal Insufficiency, Chronic / blood
  • Renal Insufficiency, Chronic / etiology
  • Thrombopoiesis / drug effects*
  • Thrombosis / blood*
  • Thrombosis / etiology

Substances

  • Hematinics
  • Isoquinolines
  • Erythropoietin
  • Glycine
  • roxadustat