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      Magnesium carbonate for phosphate control in patients on hemodialysis. A randomized controlled trial

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          Abstract

          Background

          Magnesium salts bind dietary phosphorus, but their use in renal patients is limited due to their potential for causing side effects. The aim of this study was to evaluate the efficacy and safety of magnesium carbonate (MgCO 3) as a phosphate-binder in hemodialysis patients.

          Methods

          Forty-six stable hemodialysis patients were randomly allocated to receive either MgCO 3 ( n = 25) or calcium carbonate (CaCO 3), ( n = 21) for 6 months. The concentration of Mg in the dialysate bath was 0.30 mmol/l in the MgCO 3 group and 0.48 mmol/l in the CaCO 3 group.

          Results

          Only two of 25 patients (8%) discontinued ingestion of MgCO 3 due to complications: one (4%) because of persistent diarrhea, and the other (4%) because of recurrent hypermagnesemia. In the MgCO 3 and CaCO 3 groups, respectively, time-averaged (months 1–6) serum concentrations were: phosphate (P), 5.47 vs. 5.29 mg/dl, P = ns; Ca, 9.13 vs. 9.60 mg/dl, P < 0.001; Ca × P product, 50.35 vs. 50.70 (mg/dl) 2, P = ns; Mg, 2.57 vs. 2.41 mg/dl, P = ns; intact parathyroid hormone (iPTH), 285 vs. 235 pg/ml, P < 0.01. At month 6, iPTH levels did not differ between groups: 251 vs. 212 pg/ml, P = ns. At month 6 the percentages of patients with serum levels of phosphate, Ca × P product and iPTH that fell within the Kidney Disease Outcomes Quality Initiative (K/DOQI) guidelines were similar in both groups, whereas more patients in the MgCO 3 group (17/23; 73.91%) than in the CaCO 3 group (5/20, 25%) had serum Ca levels that fell within these guidelines, with the difference being significant at P < 0.01.

          Conclusion

          Our study shows that MgCO 3 administered for a period of 6 months is an effective and inexpensive agent to control serum phosphate levels in hemodialysis patients. The administration of MgCO 3 in combination with a low dialysate Mg concentration avoids the risk of severe hypermagnesemia.

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          Most cited references21

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          Serum magnesium level and arterial calcification in end-stage renal disease.

          In this paper we examine the relationship of serum levels of Ca, P, Ca X P, P/Mg, Ca X P/Mg, alkaline phosphatase, and iPTH to the development or regression of peripheral arterial calcifications (AC) in 44 patients with end-stage renal disease being treated by continuous ambulatory peritoneal dialysis (CAPD). The average follow-up time of this longitudinal study was 27 months (range 6-67 months). The patients were divided into two groups: Group A, those showing one or more increases of AC; and Group B, patients in whom AC either did not develop or decreased during the follow-up. There was no significant difference in serum Ca, P, Ca X P, alkaline phosphatase of iPTH between the two groups. However, serum Mg was significantly lower in Group A than in Group B (2.69 +/- 0.52 and 3.02 +/- 0.51 mg/dl, respectively, P less than 0.001), while the ratios P/Mg and Ca X P/Mg were significantly higher. Our observations suggest that in end-stage renal disease hypermagnesemia may retard the development of arterial calcifications.
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            Treatment of hyperphosphatemia in hemodialysis patients: The Calcium Acetate Renagel Evaluation (CARE Study).

            Hyperphosphatemia underlies development of hyperparathyroidism, osteodystrophy, extraosseous calcification, and is associated with increased mortality in hemodialysis patients. To determine whether calcium acetate or sevelamer hydrochloride best achieves recently recommended treatment goals of phosphorus
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              Intra- and extracellular magnesium levels and atheromatosis in haemodialysis patients.

              Traditional risk factors do not adequately explain the high prevalence of cardiovascular disease in patients with chronic renal insufficiency. Currently, there is a lot of evidence that hypomagnesaemia may play a significant role in the pathogenesis of cardiovascular diseases in general population. The aim of this study was to test the hypothesis that magnesium status in haemodialysis patients is related to the degree of atheromatosis of carotid arteries, as assessed by B-mode ultrasound. Intima-media thickness of both common carotids was assessed by B-mode ultrasound in 93 stable chronic haemodialysis patients and in 182 age- and sex-matched healthy controls. Intracellular magnesium as well as serum magnesium levels were obtained in the haemodialysis patients. Intracellular magnesium was estimated by determination of this ion in isolated peripheral lymphocytes. Haemodialysis patients had also a significantly higher mean common carotid intima-media thickness than controls (0.87+/-0.16 vs 0.76+/-0.13 mm, p < 0.001). Multivariate analysis revealed that in haemodialysis patients both serum magnesium and intracellular magnesium were negatively associated with common carotid intima-media thickness (p = 0.001 and p = 0.003 respectively). Significant associations between the age of the haemodialysis patients, the existence of diabetes mellitus as well as the serum calcium x serum phosphate product with common carotid intima-media thickness of haemodialysis patients were also observed. A strong negative association of both extracellular and intracellular magnesium with common carotid intima-media thickness exists in haemodialysis patients. The above finding suggests that magnesium may play an important protective role in the development and/or acceleration of arterial atherosclerosis in patients with chronic renal insufficiency.
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                Author and article information

                Contributors
                +30-28210-43140 , +30-28210-22109 , ioatza@otenet.gr
                Journal
                Int Urol Nephrol
                International Urology and Nephrology
                Springer Netherlands (Dordrecht )
                0301-1623
                1573-2584
                10 January 2008
                March 2008
                : 40
                : 1
                : 193-201
                Affiliations
                [1 ]Department of Nephrology, General Hospital of Chania, 18, Michali Mefa St, Chania-Crete, PC 73100 Greece
                [2 ]Liwan Hospital, Guangzhou Medical College, Guangzhou, Guangdong Province P.R. China
                [3 ]Toronto Western Hospital, Toronto, Ontario Canada
                Article
                9300
                10.1007/s11255-007-9300-0
                2268719
                18193489
                a6d94656-1e55-4318-a280-4c33c9874e4a
                © The Author(s) 2008
                History
                : 29 August 2007
                : 19 October 2007
                Categories
                Original Article
                Custom metadata
                © Springer Science+Business Media, B.V. 2008

                Nephrology
                magnesium carbonate,hemodialysis,end-stage renal disease,phosphate-binders
                Nephrology
                magnesium carbonate, hemodialysis, end-stage renal disease, phosphate-binders

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