Poly[allylamine hydrochloride] (RenaGel): A noncalcemic phosphate binder for the treatment of hyperphosphatemia in chronic renal failure

被引:221
作者
Chertow, GM
Burke, SK
Lazarus, JM
Stenzel, KH
Wombolt, D
Goldberg, D
Bonventre, JV
Slatopolsky, E
机构
[1] GELTEX PHARMACEUT INC, WALTHAM, MA USA
[2] ROGOSIN INST, NEW YORK, NY USA
[3] CLIN RES ASSOCIATES TIDEWATER, NORFOLK, VA USA
[4] WASHINGTON UNIV, SCH MED, DEPT INTERNAL MED, DIV RENAL, ST LOUIS, MO 63110 USA
关键词
hyperphosphatemia; hyperparathyroidism; chronic renal failure; randomized controlled trial; cholesterol;
D O I
10.1016/S0272-6386(97)90009-3
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
Dietary phosphate restriction and the oral administration of calcium and aluminum salts have been the principal means of controlling hyperphosphatemia in individuals with end-stage renal disease over the past decade. Although relatively well-tolerated, a large fraction of patients treated with calcium develop hypercalcemia, particularly when administered concurrently with calcitriol, despite a lowering of the dialysate calcium concentration. We evaluated the efficacy of cross-linked poly[allylamine hydrochloride] (RenaGel; Geltex Pharmaceuticals, Waltham, MA), a nonabsorbable calcium- and aluminum-free phosphate binder, in a randomized, placebo-controlled, double-blind trial of 36 maintenance hemodialysis patients followed over an Ei-week period, RenaGel was found to be as effective as calcium carbonate or acetate as a phosphate hinder, The reduction in serum phosphorus was significantly greater after 2 weeks of treatment with RenaGel (6.6 +/- 2.1 mg/dL to 5.4 +/- 1.5 mg/dL) compared with placebo (7.0 +/- 2.1 mg/dL to 7.2 +/- 2.4 mg/dL; P = 0.037). There was no significant change in serum calcium concentration in either treatment group, The total serum cholesterol and low-density lipoprotein cholesterol fraction were significantly reduced in RenaGel-treated patients compared with placebo-treated patients (P = 0.013 and P = 0.003, respectively) without a concomitant reduction in high-density lipoprotein cholesterol (P = 0.93), There was no difference among recipients of RenaGel and placebo in terms of adverse events, RenaGel is a safe and effective alternative to oral calcium for the management of hyperphosphatemia in end-stage renal disease. (C) 1997 by the National Kidney Formation, Inc.
引用
收藏
页码:66 / 71
页数:6
相关论文
共 27 条
[1]   IN ADVANCED RENAL-FAILURE, DIETARY PHOSPHORUS RESTRICTION REVERSES HYPERPARATHYROIDISM INDEPENDENT OF CHANGES IN THE LEVELS OF CALCITRIOL [J].
APARICIO, M ;
COMBE, C ;
LAFAGE, MH ;
DEPRECIGOUT, V ;
POTAUX, L ;
BOUCHET, JL .
NEPHRON, 1993, 63 (01) :122-123
[2]   ALUMINUM AND THE PATHOGENESIS OF DIALYSIS ENCEPHALOPATHY [J].
ARIEFF, AI .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1985, 6 (05) :317-321
[3]  
Burke Bertha S., 1947, JOUR AMER DIETETIC ASSOC, V23, P1041
[4]  
Burkel S. K., 1996, Nephrology Dialysis Transplantation, V11, pA40
[5]   MINERALS, VITAMIN-D, AND PARATHYROID-HORMONE IN CONTINUOUS AMBULATORY PERITONEAL-DIALYSIS [J].
DELMEZ, JA ;
SLATOPOLSKY, E ;
MARTIN, KJ ;
GEARING, BN ;
HARTER, HR .
KIDNEY INTERNATIONAL, 1982, 21 (06) :862-867
[6]  
DRUEKE TB, 1986, KIDNEY INT, pS45
[7]  
GINSBURG DS, 1973, LANCET, V1, P1271
[8]  
GONELLA M, 1985, CLIN NEPHROL, V24, P147
[9]   BONE-DISEASE AND ALUMINUM - PATHOGENIC CONSIDERATIONS [J].
GOODMAN, WG .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1985, 6 (05) :330-335
[10]   CALCIUM AND PHOSPHORUS FLUXES DURING HEMODIALYSIS WITH LOW CALCIUM DIALYSATE [J].
HOU, SH ;
ZHAO, J ;
ELLMAN, CF ;
HU, J ;
GRIFFIN, Z ;
SPIEGEL, DM ;
BOURDEAU, JE .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1991, 18 (02) :217-224