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Complementary Alternative Cardiovascular Medicine

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66 <strong>Alternative</strong> <strong>Cardiovascular</strong> <strong>Medicine</strong><br />

The acute effects of 3 g of vitamin C infusion (48) was studied in 11<br />

subjects with idiopathic dilated cardiomyopathy. The authors demonstrated<br />

that endothelium dysfunction can be acutely reversed. Vitamin C<br />

is a water-soluble antioxidant and is an efficient scavenger of oxygen<br />

free radicals, suggesting an increased availability of NO.<br />

The administration of vitamin C suppresses endothelial cell apoptosis<br />

(programmed cell death), suggesting the functional benefit of vitamin C<br />

supplementation on endothelial function (49). Patients were randomized<br />

to receive vitamin C (2.5 g) or placebo, according to a sequential administration<br />

protocol combining iv bolus with oral application of the treatment<br />

(2 g vitamin C) and placebo for 3 d to patients with CHF.<br />

Vitamins have been studied in combinations, particularly vitamins C<br />

and E. In a double-blind prospective study (50), 40 patients (0–2 yr after<br />

cardiac transplantation) were randomly assigned vitamin C 500 mg plus<br />

400 IU vitamin E twice daily (n = 19) or placebo (n = 21) for 1 yr. The<br />

primary endpoint was the change in average intimal index (plaque area<br />

divided by the vessel area) measured by intravascular ultrasonography.<br />

Coronary endothelium-dependent vasoreactivity was also assessed.<br />

During the 1-yr treatment, the intimal index increased in the placebo<br />

group by 8% but did not change significantly in the treatment group<br />

(0.8%). Coronary endothelial function remained stable in both groups.<br />

This study suggested that supplementation with vitamins C and E retards<br />

the early progression of transplant-associated coronary arteriosclerosis.<br />

Supplementation with 500 mg of vitamins C, 400 IU of E and 12 mg<br />

β-carotene or 1000 mg of vitamin C, 800 IU of E, and 24 mg β-carotene<br />

did not significantly alter brachial reactivity in a 12-wk trial of 18 nonsmokers<br />

with established CAD but no diabetes (51).<br />

Niacin<br />

In patients with hyperlipidemia, niacin decreases morbidity and<br />

mortality rates (52). Niacin is most effective in increasing HDL C<br />

(53,54). The combination of statins and low-dose niacin is effective in<br />

improving the LDL C/HDL C ratio rather than the drug alone (55–58).<br />

The doses of niacin ranged from 1000 to 3000 mg/d in these studies.<br />

These doses usually have side effects, including flushing, gastrointestinal<br />

(GI) problems, and liver function test abnormalities. In a recent small<br />

study (59), the addition of very low-dose niacin 50 mg administered<br />

twice daily for 3 mo, increased the mean HDL cholesterol by 2.1 mg/dL<br />

vs –0.56 mg/dL for the placebo group (p = .0246). In addition, no major<br />

side effects were noted and no patients stopped the study medication as

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