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Am J Med Sci ; 341(2): 113-8, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21239963

ABSTRACT

INTRODUCTION: A dyshomeostasis of macro- and micronutrients, including vitamin D and oxidative stress, are common pathophysiologic features in patients with congestive heart failure (CHF). In African Americans (AA) with CHF, reductions in plasma 25(OH)D are of moderate-to-marked severity (<20 ng/mL) and may be accompanied by ionized hypocalcemia with compensatory increases in serum parathyroid hormone (PTH). The management of hypovitaminosis D in AA with CHF has not been established. METHODS: Herein, a 14-week regimen: an initial 8 weeks of oral ergocalciferol (50,000 IU once weekly); followed by a 6-week maintenance phase of cholecalciferol (1400 IU daily); and a CaCO3 (1000 mg daily) supplement given throughout was designed and tested. Fourteen AA patients having a dilated (idiopathic) cardiomyopathy with reduced ejection fraction (EF, <35%) were enrolled: all completed the initial 8-week course; and 12 complied with the full 14 weeks. At baseline, 8 and/or 14 weeks, serum 25(OH)D and PTH; serum 8-isoprostane, a biomarker of lipid peroxidation, and echocardiographic EF were monitored. RESULTS: Reduced 25(OH)D at entry (14.4 ± 1.3 ng/mL) was improved (P < 0.05) in all patients at 8 weeks (30.7 ± 3.2 ng/mL) and sustained (P < 0.05) at 14 weeks (30.9 ± 2.8 ng/mL). Serum PTH, abnormally increased in 5 patients at baseline (104.8 ± 8.2 pg/mL), was reduced at 8 and 14 weeks (74.4 ± 18.3 and 73.8 ± 13.0 pg/mL, respectively). Plasma 8-isoprostane at entry (136.1 ± 8.8 pg/mL) was reduced at 14 weeks (117.8 ± 7.8 pg/mL; P < 0.05), whereas baseline EF (24.3 ± 1.7%) was improved (31.3 ± 4.3%; P < 0.05). CONCLUSIONS: Thus, the 14-week course of supplemental vitamin D and CaCO3 led to healthy 25(OH)D levels in AA with heart failure having vitamin D deficiency of moderate-to-marked severity. Albeit a small patient population, the findings suggest that this regimen may attenuate the accompanying secondary hyperparathyroidism and oxidative stress and improve ventricular function.


Subject(s)
Calcium, Dietary/administration & dosage , Heart Failure/drug therapy , Heart Failure/etiology , Vitamin D Deficiency/complications , Vitamin D Deficiency/drug therapy , Vitamin D/administration & dosage , Black or African American , Calcium Carbonate/administration & dosage , Cardiomyopathy, Dilated/blood , Cardiomyopathy, Dilated/diet therapy , Cardiomyopathy, Dilated/drug therapy , Cardiomyopathy, Dilated/etiology , Cholecalciferol/administration & dosage , Dietary Supplements , Dinoprost/analogs & derivatives , Dinoprost/blood , Ergocalciferols/administration & dosage , Female , Heart Failure/blood , Heart Failure/diet therapy , Humans , Hyperparathyroidism, Secondary/blood , Hyperparathyroidism, Secondary/diet therapy , Hyperparathyroidism, Secondary/drug therapy , Hyperparathyroidism, Secondary/etiology , Male , Middle Aged , Parathyroid Hormone/blood , Stroke Volume , Vitamin D/analogs & derivatives , Vitamin D/blood , Vitamin D Deficiency/blood , Vitamin D Deficiency/diet therapy
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