Pilot study of dietary phosphorus restriction and phosphorus binders to target fibroblast growth factor 23 in patients with chronic kidney disease

Tamara Isakova, Orlando M Gutiérrez, Kelsey Smith, Michael Epstein, Leigh K Keating, Harald Jüppner, Myles Wolf, Tamara Isakova, Orlando M Gutiérrez, Kelsey Smith, Michael Epstein, Leigh K Keating, Harald Jüppner, Myles Wolf

Abstract

Background: High levels of fibroblast growth factor 23 (FGF23) are associated with mortality and progression of chronic kidney disease (CKD). Reducing dietary phosphorus intake lowers FGF23 secretion in healthly individuals, but there is little data on its effects in patients with pre-dialysis CKD.

Methods: Using a 2×2 factorial design, we randomly assigned 16 normophosphataemic CKD stage 3-4 patients to receive a 2-week treatment with either lanthanum carbonate 1000 mg three times daily or placebo, and to ingest a tightly controlled diet containing 750 or 1500 mg of dietary phosphorus daily. We analysed serial measurements of FGF23, parathyroid hormone, serum phosphate and calcium, and 24-h urinary phosphate and calcium excretion using repeated-measures analyses.

Results: Compared with the 1500-mg phosphorus diet, patients assigned to the 750-mg diet had greater reduction in 24-h urinary phosphate excretion (66% vs. 29%; P<0.0001). Lanthanum-treated patients experienced a significant reduction in 24-h urinary phosphate excretion compared with baseline (64%; P<0.0001), but the difference compared with placebo did not reach significance (64% vs. 31%). Despite the significant reductions in 24-h urinary phosphate excretion, no group demonstrated a significant reduction in FGF23 levels; FGF23 levels actually increased significantly in the 1500-mg diet plus placebo group, suggesting dietary phosphorus loading.

Conclusions: Although dietary phosphorus restriction and lanthanum lowered urinary phosphate excretion consistent with a rapid decrease in phosphorus absorption, inducing a reduction in FGF23 levels in CKD patients may require interventions with a longer duration than in healthy volunteers.

Figures

Fig. 1
Fig. 1
Mean absolute (A) and percent change from baseline (B) in 24-h urinary phosphate excretion during the 2-week intervention period. Error bars represent standard errors.
Fig. 2
Fig. 2
Mean 24-h urinary phosphate excretion (A), serum phosphate (B), cFGF23 (C) and iPTH (D) in participants assigned to 750-mg (n = 8) versus 1500-mg phosphorus diet (n = 8). Error bars represent standard errors.
Fig. 3
Fig. 3
Mean 24-h urinary phosphate excretion (A), serum phosphate (B), cFGF23 (C) and iPTH (D) in participants assigned to lanthanum carbonate (n = 8) versus placebo (n = 8). Error bars represent standard errors.
Fig. 4
Fig. 4
Mean percent change from baseline in cFGF23 levels during the 2-week intervention period. Error bars represent standard errors.

Source: PubMed

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