Magnesium carbonate as a phosphorus binder: A prospective, controlled, crossover study

被引:78
作者
Delmez, JA
Kelber, J
Norword, KY
Giles, KS
Slatopolsky, E
机构
[1] WASHINGTON UNIV, SCH MED, DIV RENAL, ST LOUIS, MO 63110 USA
[2] WASHINGTON UNIV, SCH MED, CHROMALLOY AMER KIDNEY CTR, ST LOUIS, MO 63110 USA
关键词
D O I
10.1038/ki.1996.22
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The use of calcium carbonate (CaCO3) to bind phosphorus (P) in chronic hemodialysis patients has been a popular tactic in the past decade. Nonetheless, problems with hypercalcemia decrease its usefulness, particularly in patients treated with calcitriol. A P binder not containing calcium (Ca) would be of value in these circumstances. In short-term studies, we showed that magnesium carbonate (MgCO3) was well-tolerated and controlled P and Mg levels when given in conjunction with a dialysate Mg of 0.6 mg/dl. We, therefore, performed a prospective, randomized, crossover study to evaluate if the chronic use of MgCO3 would allow a reduction in the dose of CaCO3 and yet achieve acceptable levels of Ca, P, and Mg. We also assessed whether the lower dose of CaCO3 would facilitate the use of larger doses of calcitriol. The two phases were MgCO3 plus half the usual dose of CaCO3 and CaCO3 alone given in the usual dose. It was found that MgCO3 (dose, 465 +/- 52 mg/day elemental Mg) allowed a decrease in the amount of elemental Ca ingested from 2.9 +/- 0.4 to 1.2 +/- 0.2 g/day (P < 0.0001). The Ca, P, Mg levels were the same in the two phases. The maximum dose of i.v. calcitriol without causing hypercalcemia was 1.5 +/- 0.3 mu g/treatment during the MgCO3 phase and 0.8 +/- 0.3 mu g/treatment during the Ca phase (P < 0.02). If these studies are confirmed, the use of MgCO3 and a dialysate Mg of 0.6 mg/dl may be considered in selected patients who develop hypercalcemia during treatment with i.v. calcitriol and CaCO3.
引用
收藏
页码:163 / 167
页数:5
相关论文
共 31 条
  • [1] Adams C.F, 1975, USDA HDB, V456
  • [2] BACHRA BN, 1969, CALCIF TISSUE RES, V3, P269
  • [3] EFFECT OF MAGNESIUM ON LIPID-INDUCED CALCIFICATION - AN INVITRO MODEL FOR BONE MINERALIZATION
    BOSKEY, AL
    POSNER, AS
    [J]. CALCIFIED TISSUE INTERNATIONAL, 1980, 32 (02) : 139 - 143
  • [4] ACTIONS OF 1 ALPHA-HYDROXYVITAMIN-D3 AND 1,25-DIHYDROXYVITAMIN-D3 ON MINERAL METABOLISM IN MAN .1. EFFECTS ON NET ABSORPTION OF PHOSPHORUS
    BRICKMAN, AS
    HARTENBOWER, DL
    NORMAN, AW
    COBURN, JW
    [J]. AMERICAN JOURNAL OF CLINICAL NUTRITION, 1977, 30 (07) : 1064 - 1069
  • [5] 1,25-DIHYDROXYVITAMIN-D3 SUPPRESSES PARATHYROID-HORMONE SECRETION FROM BOVINE PARATHYROID CELLS IN TISSUE-CULTURE
    CANTLEY, LK
    RUSSELL, J
    LETTIERI, D
    SHERWOOD, LM
    [J]. ENDOCRINOLOGY, 1985, 117 (05) : 2114 - 2119
  • [6] CLARKSON EM, 1966, CLIN SCI, V30, P425
  • [7] DELMEZ JA, 1992, J AM SOC NEPHROL, V3, P96
  • [8] MINERALS, VITAMIN-D, AND PARATHYROID-HORMONE IN CONTINUOUS AMBULATORY PERITONEAL-DIALYSIS
    DELMEZ, JA
    SLATOPOLSKY, E
    MARTIN, KJ
    GEARING, BN
    HARTER, HR
    [J]. KIDNEY INTERNATIONAL, 1982, 21 (06) : 862 - 867
  • [9] HYPERPHOSPHATEMIA - ITS CONSEQUENCES AND TREATMENT IN PATIENTS WITH CHRONIC RENAL-DISEASE
    DELMEZ, JA
    SLATOPOLSKY, E
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 1992, 19 (04) : 303 - 317
  • [10] ALUMINUM TOXICITY DURING REGULAR HEMODIALYSIS
    ELLIOTT, HL
    DRYBURGH, F
    FELL, GS
    SABET, S
    MACDOUGALL, AI
    [J]. BRITISH MEDICAL JOURNAL, 1978, 1 (6120) : 1101 - 1103