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Nephropathic Cystinosis: A Distinct Form of CKD-Mineral and Bone Disorder that Provides Novel Insights into the Regulation of FGF23.

Pablo FlorenzanoMacarena JimenezCarlos R FerreiraGalina NesterovaMary Scott RobertsSri Harsha TellaLuis Fernandez de CastroRachel I GafniMyles WolfHarald JüppnerBarbara GalesKatherine Wesseling-PerryDaniela MarkovichWilliam A GahlIsidro B SaluskyMichael T Collins
Published in: Journal of the American Society of Nephrology : JASN (2020)
Nephropathic cystinosis CKD patients have mineral abnormalities that are distinct from those in CKD stemming from other causes. Persistently increased urinary phosphate excretion maintains serum phosphate levels within the normal range, thus protecting patients with nephropathic cystinosis from elevations of FGF23 during early CKD stages. These findings support the notion that phosphate is a significant driver of increased FGF23 levels in CKD and that mineral abnormalities associated with CKD are likely to vary depending on the underlying renal disease.
Keyphrases
  • chronic kidney disease
  • end stage renal disease
  • ejection fraction
  • prognostic factors
  • bone mineral density
  • soft tissue