TY - JOUR
T1 - A 1-Year Randomized Trial of Calcium Acetate Versus Sevelamer on Progression of Coronary Artery Calcification in Hemodialysis Patients With Comparable Lipid Control
T2 - The Calcium Acetate Renagel Evaluation-2 (CARE-2) Study
AU - Qunibi, Wajeh
AU - Moustafa, Moustafa
AU - Muenz, Larry R.
AU - He, David Y.
AU - Kessler, Paul D.
AU - Diaz-Buxo, Jose A.
AU - Budoff, Mathew
N1 - Funding Information:
Financial Disclosure: Dr Qunibi is a consultant and speaker for and a recipient of research support from Fresenius Medical Care, which markets PhosLo. Dr Moustafa has received research support from Fresenius Medical Care. Dr Muenz and Mr He are paid consultants to Fresenius Medical Care. Dr Kessler is an employee of Nabi Biopharmaceutical, which previously marketed PhosLo. Dr Diaz-Buxo is an employee of Fresenius Medical Care.
PY - 2008/6
Y1 - 2008/6
N2 - Background: Previous clinical trials showed that progression of coronary artery calcification (CAC) may be slower in hemodialysis patients treated with sevelamer than those treated with calcium-based phosphate binders. Because sevelamer decreases low-density lipoprotein cholesterol (LDL-C) levels, we hypothesized that intensive lowering of LDL-C levels with atorvastatin in hemodialysis patients treated with calcium acetate would result in CAC progression rates similar to those in sevelamer-treated patients. Study Design: Randomized, controlled, open-label, noninferiority trial with an upper bound for the noninferiority margin of 1.8. Setting & Participants: 203 prevalent hemodialysis patients at 26 dialysis centers with serum phosphorus levels greater than 5.5 mg/dL, LDL-C levels greater than 80 mg/dL, and baseline CAC scores of 30 to 7,000 units assessed by means of electron-beam computed tomography. Interventions: 103 patients were randomly assigned to calcium acetate, and 100 patients to sevelamer for 12 months to achieve phosphorus levels of 3.5 to 5.5 mg/dL. Atorvastatin was added to achieve serum LDL-C levels less than 70 mg/dL in both groups. Outcomes & Measurements: The primary end point was change in CAC score assessed by means of electron-beam computed tomography. Results: After 12 months, mean serum LDL-C levels decreased to 68.8 ± 22.0 mg/dL in the calcium-acetate group and 62.4 ± 23.0 mg/dL in the sevelamer group (P = 0.3). Geometric mean increases in CAC scores were 35% in the calcium-acetate group and 39% in the sevelamer group, with a covariate-adjusted calcium acetate-sevelamer ratio of 0.994 (95% confidence interval, 0.851 to 1.161). Limitations: Treatment assignment was not blinded. The 1.8 a priori margin is large, CAC is a surrogate outcome, duration of treatment was short, and dropout rate was high. Conclusions: With intensive lowering of LDL-C levels for 1 year, hemodialysis patients treated with either calcium acetate or sevelamer experienced similar progression of CAC.
AB - Background: Previous clinical trials showed that progression of coronary artery calcification (CAC) may be slower in hemodialysis patients treated with sevelamer than those treated with calcium-based phosphate binders. Because sevelamer decreases low-density lipoprotein cholesterol (LDL-C) levels, we hypothesized that intensive lowering of LDL-C levels with atorvastatin in hemodialysis patients treated with calcium acetate would result in CAC progression rates similar to those in sevelamer-treated patients. Study Design: Randomized, controlled, open-label, noninferiority trial with an upper bound for the noninferiority margin of 1.8. Setting & Participants: 203 prevalent hemodialysis patients at 26 dialysis centers with serum phosphorus levels greater than 5.5 mg/dL, LDL-C levels greater than 80 mg/dL, and baseline CAC scores of 30 to 7,000 units assessed by means of electron-beam computed tomography. Interventions: 103 patients were randomly assigned to calcium acetate, and 100 patients to sevelamer for 12 months to achieve phosphorus levels of 3.5 to 5.5 mg/dL. Atorvastatin was added to achieve serum LDL-C levels less than 70 mg/dL in both groups. Outcomes & Measurements: The primary end point was change in CAC score assessed by means of electron-beam computed tomography. Results: After 12 months, mean serum LDL-C levels decreased to 68.8 ± 22.0 mg/dL in the calcium-acetate group and 62.4 ± 23.0 mg/dL in the sevelamer group (P = 0.3). Geometric mean increases in CAC scores were 35% in the calcium-acetate group and 39% in the sevelamer group, with a covariate-adjusted calcium acetate-sevelamer ratio of 0.994 (95% confidence interval, 0.851 to 1.161). Limitations: Treatment assignment was not blinded. The 1.8 a priori margin is large, CAC is a surrogate outcome, duration of treatment was short, and dropout rate was high. Conclusions: With intensive lowering of LDL-C levels for 1 year, hemodialysis patients treated with either calcium acetate or sevelamer experienced similar progression of CAC.
KW - Cardiovascular disease
KW - atorvastatin
KW - cholesterol
KW - dialysis
KW - dyslipidemia
KW - electron-beam computed tomography (EBCT)
KW - hyperphosphatemia
KW - low-density lipoprotein
KW - secondary hyperparathyroidism
KW - statins
KW - vascular calcification
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U2 - 10.1053/j.ajkd.2008.02.298
DO - 10.1053/j.ajkd.2008.02.298
M3 - Article
C2 - 18423809
AN - SCOPUS:43849094954
SN - 0272-6386
VL - 51
SP - 952
EP - 965
JO - American Journal of Kidney Diseases
JF - American Journal of Kidney Diseases
IS - 6
ER -