首页> 外文期刊>Clinical Pharmacology and Therapeutics >Chronotherapy of high-dose 1,25-dihydroxyvitamin D3 in hemodialysis patients with secondary hyperparathyroidism: a single-dose study.
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Chronotherapy of high-dose 1,25-dihydroxyvitamin D3 in hemodialysis patients with secondary hyperparathyroidism: a single-dose study.

机译:对继发性甲状旁腺功能亢进症的血液透析患者进行大剂量1,25-二羟基维生素D3的长期治疗:单剂量研究。

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BACKGROUND: A high-dose oral intermittent vitamin D (pulse therapy) is widely used for the treatment of secondary hyperparathyroidism associated with kidney failure. However, hypercalcemia by vitamin D sometimes interrupts this treatment. Because serum calcium concentration possesses a circadian rhythm, a chronopharmacologic approach of vitamin D may have merit for avoidance of adverse reactions. METHODS: Six female secondary hyperparathyroidism patients receiving maintenance hemodialysis received a single oral dose of 2 microg 1,25-dihydroxyvitamin D3 at either 8 AM or 8 PM in a crossover design. Serum concentrations of ionized and total calcium, phosphate, and vitamin D3 were determined for a 48-hour period after administration. We also measured serum intact parathyroid hormone before and 48 hours after dosing as an index for efficacy. RESULTS: A single oral administration of the drug caused an increase in concentration of ionized calcium, serum calcium, and phosphate. However, the area under concentration-time curve from zero to 48 hours [AUC(0-48)] and peak concentration of these variables were markedly lower after dosing at 8 PM. Pre-dose concentrations of these variables were lower at night. The AUC(0-48) of serum vitamin D3 of the morning and night trials did not differ significantly. Reduction of intact parathyroid hormone concentration was also similar between the two trials. CONCLUSION: The administration of vitamin D3 at night may reduce the occurrence of hypercalcemia and hyperphosphatemia in patients with secondary hyperparathyroidism, whereas the pharmacokinetics and intact parathyroid hormone-lowering effect of the drug does not vary with dosing time.
机译:背景:大剂量口服间歇性维生素D(脉冲疗法)被广泛用于治疗继发于肾衰竭的继发性甲状旁腺功能亢进症。但是,维生素D引起的高钙血症有时会中断这种治疗。由于血清钙浓度具有昼夜节律,因此维生素D的时序药理学方法可避免不良反应。方法:六名接受维持性血液透析的女性继发性甲状旁腺功能亢进患者在交叉设计中于上午8点或晚上8点接受了2微克1,25-二羟基维生素D3单次口服剂量。给药后48小时内,应测定血清中离子化钙,总钙,磷酸盐和维生素D3的浓度。我们还测量了给药前和给药后48小时的血清完整甲状旁腺激素水平,作为疗效指标。结果:单次口服该药物导致离子钙,血清钙和磷酸盐的浓度增加。然而,在晚上8点给药后,浓度-时间曲线下的面积从零到48小时[AUC(0-48)]和这些变量的峰值浓度明显降低。这些变量的剂量前浓度在夜间较低。早晚试验的血清维生素D3的AUC(0-48)没有显着差异。在两个试验之间,完整的甲状旁腺激素浓度的降低也相似。结论:夜间服用维生素D3可以减少继发性甲状旁腺功能亢进症患者高钙血症和高磷酸盐血症的发生,而该药的药代动力学和完整的甲状旁腺激素降低作用并不随给药时间而变化。

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