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Received March 28, 2007
Accepted on June 26, 2007
ORIGINAL ARTICLES |
Franz Volhard Clinic, Department of Nephrology and Hypertension, Medical Faculty of the Charité, HELIOS-Klinikum-Berlin, Berlin, Germany
1 To whom correspondence should be addressed. E-mail: kettritz{at}charite.de.
| Abstract |
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Background and objectives: Adverse effects complicate the use of drugs that are prescribed for phosphate control in dialysis patients. Alternative treatment options are needed.
Design, setting, participants, & measurements: Nicotinic acid inhibits intestinal phosphate reabsorption and increases HDL cholesterol. This study tested the phosphate-lowering and HDL-increasing effect of Niaspan (prolonged-release nicotinic acid) in patients who were undergoing dialysis. Efficacy, safety, and tolerability of Niaspan were prospectively studied. Twenty dialysis patients, who were receiving a stable dosage of a calcium salt–containing drug for phosphate control, received after a 2-wk washout period Niaspan for 12 wk. Patients were started on 375 mg/d, and the dosage was increased every 2 wk to achieve 500, 1000, 1500, and 2000 mg/d, respectively. Clinical and laboratory parameters were prospectively recorded in patients who tolerated a target dosage of
1000 mg/d.
Results: Seventeen patients tolerated
1000 mg/d Niaspan (mean dosage 1470 ± 110 mg/d). Niaspan treatment for 12 wk decreased serum phosphate values from 7.2 ± 0.5 to 5.9 ± 0.6 mg/dl (P < 0.015). In contrast, Niaspan did not affect serum calcium levels. A significant increase in HDL cholesterol from 40 ± 3.2 to 59 ± 5.5 mg/dl (34%) was also observed with Niaspan (P = 0.0005).
Conclusions: Niaspan effectively lowered serum phosphate levels and significantly increased HDL cholesterol. Niaspan may provide an alternative or adjunctive treatment option in dialysis patients.
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S. C. Cheng, D. O. Young, Y. Huang, J. A. Delmez, and D. W. Coyne A Randomized, Double-Blind, Placebo-Controlled Trial of Niacinamide for Reduction of Phosphorus in Hemodialysis Patients Clin. J. Am. Soc. Nephrol., July 1, 2008; 3(4): 1131 - 1138. [Abstract] [Full Text] [PDF] |
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