NDT Plus Advance Access first published online on August 11, 2008
This version published online on September 6, 2008
NDT Plus, doi:10.1093/ndtplus/sfn128
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The administration of cinacalcet hydrochloride just before a haemodialysis session suppresses the transient rise in intact parathyroid hormone induced by a low-calcium dialysate: when should cinacalcet hydrochloride be administered?
1 Jin-Ai-Kai Date Clinic, Kidney Dialysis Center, Asahikawa Hokkaido, 070-0061
2 Discovery Research Laboratories Kirin Pharma Co. Ltd, Takasaki Gunma, 370-1295, Japan
Correspondence: E-mail: dateclinic{at}mc.neweb.ne.jp
Sir,
Parathyroid cells can sense small changes in plasma calcium ion (Ca2+) levels by virtue of a cell surface calcium receptor (CaR). Calcimimetics such as R-568 and cinacalcet hydrochloride (cinacalcet) are positive allosteric modulators that activate CaRs and thereby suppress parathyroid hormone (PTH) secretion [1]. Clinical trials have demonstrated that cinacalcet treatment lowers not only the serum PTH but also the serum Ca levels in haemodialysis (HD) patients with secondary hyperparathyroidism (2HPT) [1]. In clinical use, the dosage of cinacalcet is not restricted by the time of the HD session because HD does not affect the pharmacokinetics of this compound [2]; this is attributed to cinacalcet's high binding capacity to plasma proteins.
The use of a so-called low-Ca dialysate (2.5 mEq/L) can increase the usage opportunities and doses of vitamin D drugs and Ca-containing phosphate binders. During each HD session, diffusion is the main route of Ca2+ transport, and the rate of passage of a given dialysate Ca2+ across the membrane depends on the direction and magnitude of its concentration gradient between the blood and dialysate [3]. Therefore, many HD patients show a transient elevation in serum PTH levels in response to the decreased plasma Ca2+ levels at the end of every HD session with a low-Ca dialysate [4]. In our experience, injection of calcitriol or its analogue (maxacalcitol) just before the HD session has failed to suppress this elevation in PTH levels. Here, we report that if cinacalcet is administered just before an HD session, it successfully suppresses the increase in the intact PTH (i-PTH) induced by a low-Ca dialysate.
The subjects of this study were 14 HD patients (9 female subjects) with a mean age of 58.5 ± 9.0 (SD) years and an HD vintage of 19.8 ± 9.4 (SD) years. All the patients had been diagnosed as 2HPT with parathyroid gland (PG) nodular hyperplasia on the basis of the findings of ultrasonography (maximum PG volume 
500 mm3 or maximum PG diameter 10 mm) and had been treated with intravenous calcitriol or maxacalcitol. Before the cinacalcet treatment started, an HD session (2.5 mEq/L Ca dialysate, 4 h in 10 patients and 4.5 h in 4 patients) significantly decreased the plasma Ca2+ levels and increased the serum i-PTH levels (Figure 1A). One week after the cinacalcet treatment (25 mg, daily), the basal levels of the serum i-PTH and plasma Ca2+ decreased (Figure 1B, Pre-HD). Cinacalcet (25 mg) administered just before the HD session caused a significant further decrease in the serum i-PTH levels without affecting the plasma Ca2+ levels (Figure 1B, Post-HD). During the subsequent cinacalcet treatment (25 mg, daily, for another 3 weeks), we increased the dose of calcitriol or maxacalcitol to prevent hypocalcaemia. Consequently, the plasma Ca2+ levels recovered to the baseline levels and the serum i-PTH levels decreased further (Figure 1C, Pre-HD). Once more, the administration of cinacalcet (25 mg) just before the HD session caused a significant further decrease in the serum i-PTH levels despite a significant reduction in the plasma Ca2+ levels (Figure 1C, Post-HD).
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Even if an elevation in PTH levels is transient, it should be avoided that basal high PTH levels increase further at the end of every HD session with a low-Ca dialysate. In addition, a transient decrease in plasma Ca2+ levels can stimulate not only PTH secretion but also PG cell proliferation. Over the long term, PG hyperplasias often progress from diffuse to nodular forms. We have demonstrated that calcimimetics are powerful inhibitors of PG cell proliferation in rats with 2HPT, regardless of calcimimetic-induced hypocalcaemia [1,5]. Therefore, we propose that cinacalcet should be administered just before HD sessions to prevent the hyperfunctioning of PG cells that is induced by the transient hypocalcaemia caused by a low-Ca dialysate. This seems to be reasonable because the maximal plasma concentration (Cmax) of cinacalcet is achieved 4–6 h after its oral administration [2]. Further investigations are clearly required to determine when cinacalcet should be administered, especially in the context of bone metabolism and the gastrointestinal adverse effects.
Conflict of interest statement. Other than N.N. who is a scientist at Kirin Pharma that manufactures and sells cinacalcet in Asia, none of the authors have reported any conflict of interest.
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 Top Notes References |
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The original article was incorrect. Figure 1a has been updated.
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TopNotesReferences |
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- Nagano N. Pharmacological and clinical properties of calcimimetics: calcium receptor activators that afford an innovative approach to controlling hyperparathyroidism. Pharmacol Ther (2006) 109:339–365.[CrossRef][Web of Science][Medline]
- Ohashi N, Uematsu T, Nagashima S, et al. The calcimimetic agent KRN 1493 lowers plasma parathyroid hormone and ionized calcium concentrations in patients with chronic renal failure on haemodialysis both on the day of haemodialysis and on the day without haemodialysis. Br J Clin Pharmacol (2004) 57:726–734.[CrossRef][Web of Science][Medline]
- Olbricht CJ, Frei U, Koch KM. Haemodialysis, complications during haemodialysis, and adequate of haemodialysis. Oxford Textbook of Clinical Nephrology—Cameron S, Davison AM, Grünfeld J-P, Kerr D, Ritz E, eds. (1992) 2. Oxford: Oxford University Press. 1417–1436.
- Kitahara T, Ueki K, Kuroiwa T, et al. Secretion of parathyroid hormone oscillates depending on the change in serum ionized calcium during hemodialysis and may affect bone metabolism. Nephron Clin Pract (2005) 101:c9–c17.[CrossRef][Web of Science][Medline]
- Wada M, Nagano N. Control of parathyroid cell growth by calcimimetics. Nephrol Dial Transplant (2003) 18(Suppl_3):iii13–iii17.
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