» Articles » PMID: 23787550

A Comparison of Calcium Acetate/magnesium Carbonate and Sevelamer-hydrochloride Effects on Fibroblast Growth Factor-23 and Bone Markers: Post Hoc Evaluation from a Controlled, Randomized Study

Overview
Date 2013 Jun 22
PMID 23787550
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Different phosphate binders exert differing effects on bone mineral metabolism and levels of regulating hormones. The objective of this post hoc evaluation of the CALcium acetate MAGnesium carbonate (CALMAG) study was to compare the effects of calcium acetate/magnesium carbonate (CaMg) and a calcium-free phosphate binder, sevelamer-hydrochloride (HCl), on serum levels of fibroblast growth factor-23 (FGF-23) and markers of bone turnover.

Methods: This secondary analysis of the controlled, randomized CALMAG study, comparing the effect of CaMg and sevelamer-HCl on serum phosphorus (P), aimed to investigate the parameters described above. The analysis included 204 patients who completed the initial study per protocol (CaMg, n = 105; sevelamer-HCl, n = 99).

Results: The study showed that serum levels of FGF-23 were significantly reduced with CaMg and sevelamer-HCl, with no difference between groups at Week 25 [analysis of covariance (ANCOVA); log-intact FGF-23 (iFGF-23), P = 0.1573]. FGF-23 levels strongly correlated with serum P levels at all time points in both groups. The bone turnover parameters alkaline phosphatase (AP), bone AP (BAP), procollagen type 1 amino-terminal propeptide 1 (P1NP), osteoprotegerin (OPG), beta-crosslaps (β-CTX) and tartrate-resistant acid phosphatase 5b (TRAP 5b) increased significantly in the sevelamer-HCl group; they remained almost unchanged in the CaMg group, after the initial phase of P lowering (ANCOVA, P < 0.0001 for all except OPG, P = 0.1718).

Conclusions: CaMg and sevelamer-HCl comparably lower serum levels of iFGF-23. Changes in bone parameters were dependent on characteristics of the phosphate binder; in contrast with sevelamer-HCl, CaMg had no influence on bone turnover markers.

Citing Articles

A network meta-analysis of therapies for hyperphosphatemia in CKD based on randomized trials.

Zheng C, Liu J, Wang T, Hu H, Chen Y Sci Rep. 2025; 15(1):2012.

PMID: 39814766 PMC: 11736078. DOI: 10.1038/s41598-024-84942-8.


Phosphorous metabolism and manipulation in chronic kidney disease.

Marando M, Tamburello A, Salera D, Di Lullo L, Bellasi A Nephrology (Carlton). 2024; 29(12):791-800.

PMID: 39433296 PMC: 11579558. DOI: 10.1111/nep.14407.


Role and Treatment of Insulin Resistance in Patients with Chronic Kidney Disease: A Review.

Nakashima A, Kato K, Ohkido I, Yokoo T Nutrients. 2021; 13(12).

PMID: 34959901 PMC: 8707041. DOI: 10.3390/nu13124349.


Effectiveness of fibroblast growth factor 23 lowering modalities in chronic kidney disease: a systematic review and meta-analysis.

Takkavatakarn K, Wuttiputhanun T, Phannajit J, Praditpornsilpa K, Eiam-Ong S, Susantitaphong P Int Urol Nephrol. 2021; 54(2):309-321.

PMID: 33797709 DOI: 10.1007/s11255-021-02848-0.


Hyperphosphatemia and Cardiovascular Disease.

Zhou C, Shi Z, Ouyang N, Ruan X Front Cell Dev Biol. 2021; 9:644363.

PMID: 33748139 PMC: 7970112. DOI: 10.3389/fcell.2021.644363.


References
1.
Iwata Y, Wada T, Yokoyama H, Toyama T, Kitajima S, Okumura T . Effect of sevelamer hydrochloride on markers of bone turnover in Japanese dialysis patients with low biointact PTH levels. Intern Med. 2007; 46(8):447-52. DOI: 10.2169/internalmedicine.46.6338. View

2.
Block G, Klassen P, Lazarus J, Ofsthun N, Lowrie E, Chertow G . Mineral metabolism, mortality, and morbidity in maintenance hemodialysis. J Am Soc Nephrol. 2004; 15(8):2208-18. DOI: 10.1097/01.ASN.0000133041.27682.A2. View

3.
Bichara M, Mercier O, Borensztein P, Paillard M . Acute metabolic acidosis enhances circulating parathyroid hormone, which contributes to the renal response against acidosis in the rat. J Clin Invest. 1990; 86(2):430-43. PMC: 296745. DOI: 10.1172/JCI114729. View

4.
Tentori F, Blayney M, Albert J, Gillespie B, Kerr P, Bommer J . Mortality risk for dialysis patients with different levels of serum calcium, phosphorus, and PTH: the Dialysis Outcomes and Practice Patterns Study (DOPPS). Am J Kidney Dis. 2008; 52(3):519-30. DOI: 10.1053/j.ajkd.2008.03.020. View

5.
DHaese P, Couttenye M, Lamberts L, Elseviers M, Goodman W, Schrooten I . Aluminum, iron, lead, cadmium, copper, zinc, chromium, magnesium, strontium, and calcium content in bone of end-stage renal failure patients. Clin Chem. 1999; 45(9):1548-56. View