Takahashi Yutaka, Tanaka Araki, Nakamura Tsukasa, Fukuwatari Tsutomu, Shibata Katsumi, Shimada Noriaki, Ebihara Isao, Koide Hikaru
Department of Medicine, Koto Hospital, Tokyo, Japan.
Kidney Int. 2004 Mar;65(3):1099-104. doi: 10.1111/j.1523-1755.2004.00482.x.
The use of calcium- or aluminum-based phosphate binders against hyperphosphatemia is limited by the adverse effects of hypercalcemia or aluminum toxicity in long-term hemodialysis. Because nicotinamide is an inhibitor of sodium-dependent phosphate cotransport in rat renal tubule and small intestine, we examined whether nicotinamide reduces serum levels of phosphorus and intact parathyroid hormone (iPTH) in patients undergoing hemodialysis.
Sixty-five hemodialysis patients with a serum phosphorus level of more than 6.0 mg/dL after a 2-week washout of calcium carbonate were enrolled in this study. Nicotinamide was administered for 12 weeks. The starting dose was 500 mg/day, and the dose was increased by 250 mg/day every 2 weeks until serum phosphorus levels were well controlled at less than 6.0 mg/dL. A 2-week posttreatment washout period followed the cessation of nicotinamide. Blood samples were collected every week for measurement of serum calcium, phosphorus, lipids, iPTH, and blood nicotinamide adenine dinucleotide (NAD).
The mean dose of nicotinamide was 1080 mg/day. The mean blood NAD concentration increased from 9.3 +/- 1.9 nmol/105 erythrocytes before treatment to 13.2 +/- 5.3 nmol/105 erythrocytes after treatment (P < 0.01). The serum phosphorus concentration increased from 5.4 +/- 1.5 mg/dL to 6.9 +/- 1.5 mg/dL with the pretreatment washout, then decreased to 5.4 +/- 1.3 mg/dL after the 12-week nicotinamide treatment (P < 0.0001), and rose again to 6.7 +/- 1.6 mg/dL after the posttreatment washout. Serum calcium levels decreased during the pretreatment washout from 9.1 +/- 0.8 mg/dL to 8.7 +/- 0.7 mg/dL with the cessation of calcium carbonate. No significant changes in serum calcium levels were observed during nicotinamide treatment. Median serum iPTH levels increased with pretreatment washout from 130.0 (32.8 to 394.0) pg/mL to 200.0 (92.5 to 535.0) pg/mL and then decreased from the maximum 230.0 (90.8 to 582.0) pg/mL to 150.0 (57.6 to 518.0) pg/mL after the 12-week nicotinamide treatment (P < 0.05). With nicotinamide, serum high-density lipoprotein (HDL) cholesterol concentrations increased from 47.4 +/- 14.9 mg/dL to 67.2 +/- 22.3 mg/dL (P < 0.0001) and serum low-density lipoprotein (LDL) cholesterol concentrations decreased from 78.9 +/- 18.8 mg/dL to 70.1 +/- 25.3 mg/dL (P < 0.01); serum triglyceride levels did not change significantly.
Nicotinamide may provide an alternative for controlling hyperphosphatemia and hyperparathyroidism without inducing hypercalcemia in hemodialysis patients.
钙基或铝基磷酸盐结合剂用于治疗高磷血症,因长期血液透析中高钙血症或铝中毒的不良反应而受到限制。由于烟酰胺是大鼠肾小管和小肠中钠依赖性磷酸盐共转运的抑制剂,我们研究了烟酰胺是否能降低血液透析患者的血清磷水平和完整甲状旁腺激素(iPTH)水平。
65例血液透析患者在停用碳酸钙2周后血清磷水平超过6.0mg/dL,纳入本研究。给予烟酰胺治疗12周。起始剂量为500mg/天,每2周剂量增加250mg/天,直至血清磷水平良好控制在6.0mg/dL以下。烟酰胺停用后有2周的治疗后洗脱期。每周采集血样,检测血清钙、磷、脂质、iPTH和血液烟酰胺腺嘌呤二核苷酸(NAD)。
烟酰胺的平均剂量为1080mg/天。血液NAD平均浓度从治疗前的9.3±1.9nmol/105红细胞增加到治疗后的13.2±5.3nmol/105红细胞(P<0.01)。血清磷浓度在预处理洗脱期从5.4±1.5mg/dL增加到6.9±1.5mg/dL,在12周烟酰胺治疗后降至5.4±1.3mg/dL(P<0.0001),治疗后洗脱期又升至6.7±1.6mg/dL。血清钙水平在预处理洗脱期随着碳酸钙的停用从9.1±0.8mg/dL降至8.7±0.7mg/dL。在烟酰胺治疗期间未观察到血清钙水平有显著变化。血清iPTH水平中位数在预处理洗脱期从130.0(32.8至394.0)pg/mL增加到200.0(92.5至535.0)pg/mL,在12周烟酰胺治疗后从最高值230.0(90.8至582.0)pg/mL降至150.0(57.6至518.0)pg/mL(P<0.05)。使用烟酰胺时,血清高密度脂蛋白(HDL)胆固醇浓度从47.4±14.9mg/dL增加到67.2±22.3mg/dL(P<0.0001),血清低密度脂蛋白(LDL)胆固醇浓度从78.9±18.8mg/dL降至70.1±25.3mg/dL(P<0.01);血清甘油三酯水平无显著变化。
烟酰胺可能为血液透析患者控制高磷血症和甲状旁腺功能亢进提供一种替代方法,且不会诱发高钙血症。