Nephrogenic systemic fibrosis is associated with hypophosphataemia: A case-control study

Elana J. Bernstein*, Tamara Isakova, Mary E. Sullivan, Lori B. Chibnik, Myles Wolf, Jonathan Kay

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Objective: Nephrogenic systemic fibrosis (NSF) is an iatrogenic fibrosing disorder that primarily affects individuals with chronic kidney disease (CKD) following exposure to gadolinium-based contrast agents (GBCAs). Derangements of calcium and phosphorus have been reported in patients with NSF. The aim of this study was to investigate potential factors in addition to GBCA exposure that may be involved in the pathogenesis of NSF. We hypothesized that patients with stage 5 CKD and NSF would manifest greater alterations in calcium, phosphorus and fibroblast growth factor 23 (FGF23) levels than those who do not have NSF. Methods: Levels of phosphorus, calcium, FGF23 and 25-hydroxy-vitamin D were measured in 10 patients with stage 5 CKD and biopsy-proven NSF and in 19 patients with stage 5 CKD without NSF. Statistical analyses were performed using Fisher's exact test for categorical variables and the Kruskal-Wallis test for continuous variables. Results: Patients with NSF had significantly lower phosphorus levels compared with controls (P = 0.01). There were no significant differences between NSF patients and controls in calcium, 25-hydroxy-vitamin D, intact parathyroid hormone or FGF23 levels. Conclusion: Differences in phosphorus metabolism may exist between patients with stage 5 CKD and NSF compared with patients with stage 5 CKD without NSF.

Original languageEnglish (US)
Article numberkeu151
Pages (from-to)1613-1617
Number of pages5
JournalRheumatology (United Kingdom)
Volume53
Issue number9
DOIs
StatePublished - Sep 2014

Keywords

  • Chronic kidney disease
  • Dialysis
  • Fibroblast growth factor 23
  • Gadolinium
  • Magnetic resonance imaging
  • Nephrogenic systemic fibrosis
  • Phosphorus

ASJC Scopus subject areas

  • Rheumatology
  • Pharmacology (medical)

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