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

Stanley M.H. Yeung(University Medical Center Groningen), S. Heleen Binnenmars(University Medical Center Groningen), Christina M. Gant(University Medical Center Groningen), Gerjan Navis(University Medical Center Groningen), Ron T. Gansevoort(University Medical Center Groningen), Stephan J. L. Bakker(University Medical Center Groningen), Martin H. de Borst(University Medical Center Groningen), Gozewijn D. Laverman(University Medical Center Groningen)
Diabetes Care
September 5, 2019
Cited by 30Open Access
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Abstract

OBJECTIVE: To 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 METHODS: . Associations of FGF23 with all-cause mortality and major adverse cardiovascular events (MACE) were studied by Cox regression. RESULTS: During 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. CONCLUSIONS: In patients with type 2 diabetes and normal or mildly impaired kidney function, FGF23 is associated with an increased risk of cardiovascular events and mortality.


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