INFLUENCE OF CALCIUM ACETATE OR CALCIUM CITRATE ON INTESTINAL ALUMINUM ABSORPTION

被引:65
作者
NOLAN, CR [1 ]
CALIFANO, JR [1 ]
BUTZIN, CA [1 ]
机构
[1] WILFORD HALL USAF MED CTR,CLIN INVEST DIRECTORATE,LACKLAND AFB,TX 78236
关键词
D O I
10.1038/ki.1990.294
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 risk of aluminum (Al) accumulation in patients with chronic renal failure has led to use of non-Al phosphate binders. Frequently, Al and non-Al phosphate binders are co-administered. Unfortunately, calcium citrate (Ca citr), when given with Al-gel, markedly enhances Al absorption. To determine whether calcium acetate (Ca acetate) also augments Al absorption, 10 normal volunteers were each given orally, three-day courses of the following drug combinations dosed four times daily: 1) aluminum hydroxide gel (Al[OH]3) (5 ml) alone; 2) Al[OH]3 (5 ml) plus Ca acetate (1330 mg); 3) Al[OH]3 (5 ml) plus Ca citr (950 mg). A nine day wash-out occurred between each course. Al levels were measured using flameless atomic absorption spectrophotometry. Daily urine Al excretion was measured during a two-day baseline before each course and during each three-day drug course. Plasma Al was obtained during each baseline and drug course. Mean 24-hour Al excretion (μg/g creatinine/day) at baseline versus treatment for each combination was: 1) 5.9 ± 3.2 versus 42.0 ± 40.7 (mean ± SD); 2) 5.7 ± 3.0 versus 40.3 ± 28.6: 3) 6.3 ± 3.4 versus 175.8 ± 103.3. Al excretion was significantly greater with combination 3 than with either 1 or 2 (P < 0.05). The difference between 1 and 2 was not significant. Plasma Al (μg/liter) at baseline versus treatment for each combination was: 1) 5.3 ± 4.2 versus 8.1 ± 2.5 (mean ± SD); 2) 3.1 ± 2.2 versus 7.3 ± 2.9; 3) 3.0 ± 2.3 versus 12.0 ± 6.1. Comparing baseline to treatment differences, the increment in plasma Al with combination 3 was significantly greater than with either 1 or 2 (P < 0.05). The difference between 1 and 2 was not significant. We conclude that in normal subjects, standard doses of Ca citr markedly enhance Al absorption from Al[OH]3, whereas Ca acetate does not augment Al absorption. Theoretically, use of Ca acetate may be associated with less risk than Ca citr for Al absorption and accumulation in patients with chronic renal failure, concurrently treated with Al-gel.
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页码:937 / 941
页数:5
相关论文
共 45 条
[1]   ALUMINUM [J].
ALFREY, AC .
ADVANCES IN CLINICAL CHEMISTRY, 1983, 23 :69-91
[2]   DIALYSIS ENCEPHALOPATHY SYNDROME - POSSIBLE ALUMINUM INTOXICATION [J].
ALFREY, AC ;
LEGENDRE, GR ;
KAEHNY, WD .
NEW ENGLAND JOURNAL OF MEDICINE, 1976, 294 (04) :184-188
[3]  
ALFREY AC, 1986, KIDNEY INT S18, V29, pS53
[4]  
ALFREY AC, 1986, KIDNEY INT S18, V29, pS8
[5]   ALUMINUM INTOXICATION FROM ALUMINUM-CONTAINING PHOSPHATE BINDERS IN CHILDREN WITH AZOTEMIA NOT UNDERGOING DIALYSIS [J].
ANDREOLI, SP ;
BERGSTEIN, JM ;
SHERRARD, DJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (17) :1079-1084
[6]   EARLY DEPOSITION OF ALUMINUM IN BONE IN DIABETIC-PATIENTS ON HEMODIALYSIS [J].
ANDRESS, DL ;
KOPP, JB ;
MALONEY, NA ;
COBURN, JW ;
SHERRARD, DJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (06) :292-296
[7]  
BAKIR AA, 1986, T AM SOC ART INT ORG, V32, P171
[8]   ALUMINUM INDUCED ANEMIA - PATHOGENESIS AND TREATMENT IN PATIENTS ON CHRONIC-HEMODIALYSIS [J].
BIA, MJ ;
COOPER, K ;
SCHNALL, S ;
DUFFY, T ;
HENDLER, E ;
MALLUCHE, H ;
SOLOMON, L .
KIDNEY INTERNATIONAL, 1989, 36 (05) :852-858
[9]   CELLULAR MECHANISM OF INTESTINAL PERMEABILITY ALTERATIONS PRODUCED BY CHELATION DEPLETION [J].
CASSIDY, MM ;
TIDBALL, CS .
JOURNAL OF CELL BIOLOGY, 1967, 32 (03) :685-+
[10]   CONTROL OF SERUM PHOSPHORUS IN UREMIA [J].
COBURN, JW ;
SALUSKY, IB .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (17) :1140-1142