This is why only small amounts of the unmodified NAM appear in the urine—even after administration of pharmacological (high) doses of the compound. 1.4 Therapeutic Efficacy A number of clinical studies have explored the potential value of niacin and its analogs in phosphate control in dialysis patients [25]. Some have shown that nicotinic acid is effective in the treatment of hyperphosphatemia [44–47] as well as hyperlipidemia (historical use). In vivo conversion of nicotinic acid to NAM is required for this action. We focus on NAM in this respect. Table 2 summarizes

the results of clinical studies of NAM in dialysis patients. Table 2 Clinical studies of nicotinamide (NAM) for the treatment of hyperphosphatemia in dialysis patients References Type of study Number of ESRD patients Number of Selleck ABT737 patients on NAM NAM dose (mg/day) Time exposed (weeks) Change in blood phosphate (%) Phosphate binders Takahashi et al. [48] Open-label 65 65 500–1,750 12 −21 Calcium carbonate Cheng et al. this website [49] Prospective,

double-blind, placebo-controlled, randomized, cross-over 33 25 500–1,500 8 −15 Phosphate binder Young et al. [50] Prospective, double-blind, placebo-controlled, randomized 15 8 750–2,250 8 −12 Phosphate binder Shahbazian et al. [51] Prospective, double-blind, placebo-controlled, randomized 48 24 500–1,000 8 −21 Phosphate binder Vasantha et al. [52] Prospective, open-label 30 30 750 8 −34 None ESRD end-stage renal disease The first study to show that NAM decreased serum phosphorus (from 6.9 to 5.4 mg/dL) Arachidonate 15-lipoxygenase and iPTH (without increasing serum calcium levels)

was published by Takahashi et al. [48]. This open-label study was carried out in 65 hyperphosphatemic dialysis patients receiving NAM in divided doses (mean daily dose 1,080 mg) for 12 weeks. Furthermore, NAM treatment significantly increased serum HDL cholesterol levels and decreased LDL cholesterol levels over the course of the study. Other authors have since reported significant reductions in phosphatemia in NAM-treated dialysis patients [49–52]. Cheng et al. [49] were the first to perform a double-blind, placebo-controlled, randomized clinical trial of NAM (300–1,800 mg) in the treatment of hyperphosphatemia in 33 dialysis patients. After 8 weeks of treatment, the mean serum phosphate level had fallen significantly in the NAM group (from 6.26 to 5.47 mg/dL) but not in the placebo group (with a rise from 5.85 to 5.98 mg/dL, in fact). Moreover, mean serum HDL levels rose in the NAM group (from 50 to 61 mg/dL) but not in the placebo group. Nicotinamide had no effect on serum calcium levels in the study population [49]. In another prospective, randomized, double blind, placebo-controlled trial of NAM in 15 dialysis patients, it was found that an initial daily dose of 750 mg of NAM resulted in a slight but significant decrease in plasma phosphorus levels (from 5.9 to 5.2 mg/dL) in the active treatment group (but not in the placebo group) at 8 weeks [50].