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Effects of dapagliflozin and dapagliflozin-saxagliptin on erythropoiesis, iron and inflammation markers in patients with type 2 diabetes and chronic kidney disease: data from the DELIGHT trial

  • Akihiko Koshino
  • , Brendon L. Neuen
  • , Niels Jongs
  • , Carol Pollock
  • , Peter J. Greasley
  • , Eva Marie Andersson
  • , Ann Hammarstedt
  • , Cecilia Karlsson
  • , Anna Maria Langkilde
  • , Takashi Wada
  • , Hiddo J.L. Heerspink*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

24 Citations (Scopus)
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Abstract

Background: This post-hoc analysis of the DELIGHT trial assessed effects of the SGLT2 inhibitor dapagliflozin on iron metabolism and markers of inflammation. Methods: Patients with type 2 diabetes and albuminuria were randomized to dapagliflozin, dapagliflozin and saxagliptin, or placebo. We measured hemoglobin, iron markers (serum iron, transferrin saturation, and ferritin), plasma erythropoietin, and inflammatory markers (urinary MCP-1 and urinary/serum IL-6) at baseline and week 24. Results: 360/461 (78.1%) participants had available biosamples. Dapagliflozin and dapagliflozin-saxagliptin, compared to placebo, increased hemoglobin by 5.7 g/L (95%CI 4.0, 7.3; p < 0.001) and 4.4 g/L (2.7, 6.0; p < 0.001) and reduced ferritin by 18.6% (8.7, 27.5; p < 0.001) and 18.4% (8.7, 27.1; p < 0.001), respectively. Dapagliflozin reduced urinary MCP-1/Cr by 29.0% (14.6, 41.0; p < 0.001) and urinary IL-6/Cr by 26.6% (9.1, 40.7; p = 0.005) with no changes in other markers. Conclusions: Dapagliflozin increased hemoglobin and reduced ferritin and urinary markers of inflammation, suggesting potentially important effects on iron metabolism and inflammation. Trial registration: ClinicalTrials.gov NCT02547935.

Original languageEnglish
Article number330
Number of pages7
JournalCardiovascular Diabetology
Volume22
Issue number1
DOIs
Publication statusPublished - Dec-2023

Keywords

  • Anemia
  • Ferritin
  • Hematopoiesis
  • Interleukin-6
  • Iron metabolism
  • Monocyte chemoattractant protein-1
  • Sodium glucose co-transporter 2 inhibitors
  • Transferrin

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