American Journal of Kidney Diseases
Volume 52, Issue 6 , Pages 1151-1157, December 2008

Phosphatemic Effect of Cinacalcet in Kidney Transplant Recipients With Persistent Hyperparathyroidism

  • Andreas L. Serra, MD

      Affiliations

    • Clinic for Nephrology, University Hospital, Switzerland
    • Zürich Center for Integrative Human Physiology, University of Zürich, Switzerland
    • Corresponding Author InformationAddress correspondence to Andreas L. Serra, MD, Clinic for Nephrology, University Hospital, Rämistrasse 100, 8091 Zürich, Switzerland
  • ,
  • Claudia Wuhrmann, MSc

      Affiliations

    • Zürich Center for Integrative Human Physiology, University of Zürich, Switzerland
  • ,
  • Rudolf P. Wüthrich, MD

      Affiliations

    • Clinic for Nephrology, University Hospital, Switzerland
    • Zürich Center for Integrative Human Physiology, University of Zürich, Switzerland

Received 5 May 2008; accepted 4 August 2008. published online 28 October 2008.

Background

In kidney transplant recipients, persistent hyperparathyroidism leads to hypercalcemia and increased urinary phosphorus excretion. The calcimimetic drug cinacalcet effectively decreases parathyroid hormone (PTH) levels and corrects hypercalcemia in these patients. The purpose of the present study is to examine the effect of cinacalcet treatment on determinants of renal phosphorus reabsorption under steady-state conditions.

Study Design

Open-label prospective uncontrolled trial.

Setting & Participants

10 stable kidney transplant recipients with persistent hyperparathyroidism.

Intervention

Cinacalcet, 30 and 60 mg/d, for 2 weeks.

Outcomes & Measures

Changes in urinary phosphorus excretion in timed urine samples, intact and carboxy-terminal (C-term) fibroblast growth factor 23 (FGF-23), intact PTH, venous pH, and bicarbonate values at defined intervals over 24 hours.

Results

Cinacalcet decreased renal phosphorus excretion in the first 8 hours by 30% to 40%, but not from 8 to 24 hours after drug administration. Serum phosphorus levels normalized in all patients. Cinacalcet markedly decreased plasma intact PTH levels (60%; P < 0.001). Cinacalcet also decreased mean intact FGF-23 levels from 67 ± 8 (SE) to 51 ± 5 and to 54 ± 6 pg/mL (P < 0.001) and mean C-term FGF-23 levels from 108 ± 15 to 87 ± 9 and to 101 ± 9 RU/mL (P < 0.01), respectively. There was high correlation between intact FGF-23 and C-term FGF-23 levels (r = 0.598; P < 0.001). Acid-base status was unchanged.

Limitations

This is a small study and does not examine the long-term effect of cinacalcet treatment.

Conclusions

Cinacalcet effectively corrected urinary phosphate wasting in kidney transplant recipients, resulting in normalization of serum phosphorus levels. The phosphatemic effects of cinacalcet correlated with a marked decrease in the phosphaturic hormone PTH, rather than with a change in FGF-23 levels or acid-base status, highlighting the importance of PTH in posttransplantation hypophosphatemia.

Index Words: Cinacalcet, hyperparathyroidism, parathyroid hormone (PTH), fibroblast growth factor 23 (FGF-23), phosphorus, renal transplantation

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 Originally published online as doi:10.1053/j.ajkd.2008.08.012 on October 28, 2008.

PII: S0272-6386(08)01304-8

doi:10.1053/j.ajkd.2008.08.012

American Journal of Kidney Diseases
Volume 52, Issue 6 , Pages 1151-1157, December 2008