Fibroblast Growth Factor 23 and Mortality in Patients With Type 2 Diabetes and Normal or Mildly Impaired Kidney Function.

  • Stanley Yeung
  • , S.H. Binnenmars
  • , Cristina M. Gant
  • , Gerjan Navis
  • , Ron T. Gansevoort
  • , Stephan J.L. Bakker
  • , Martin De Borst
  • , GD Laverman

Research output: Contribution to journalArticleAcademicpeer-review

25 Citations (Scopus)

Abstract

ObjectiveTo study whether fibroblast growth factor 23 (FGF23) is associated with adverse outcomes in patients with type 2 diabetes and normal or mildly impaired kidney function.Research design and methodsWe analyzed C-terminal FGF23 levels in 310 patients with type 2 diabetes and estimated glomerular filtration rate ≥60 mL/min/1.73 m2. Associations of FGF23 with all-cause mortality and major adverse cardiovascular events (MACE) were studied by Cox regression.ResultsDuring a follow-up of 5.8 years (3.3-6.5), 47 patients developed MACE and 28 patients died. FGF23 was associated with an increased risk of all-cause mortality (age- and sex-adjusted hazard ratio 2.78 [95% CI 1.76-4.40]) and MACE (1.67 [1.12-2.49]). Results were similar after additional adjustment for other potential confounders and were consistent upon replication in an independent cohort.ConclusionsIn patients with type 2 diabetes and normal or mildly impaired kidney function, FGF23 is associated with an increased risk of cardiovascular events and mortality.
Original languageEnglish
JournalDiabetes care
Volume42
Issue number11
DOIs
Publication statusPublished - 5 Sept 2019

Keywords

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