口服paricalcitol。

Emma D Deeks, Katherine A Lyseng-Williamson
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引用次数: 0

摘要

paricalcitol口服制剂已被开发用于预防和治疗3期或4期慢性肾脏疾病患者的继发性甲状旁腺功能亢进。黑三角Paricalcitol是一种合成的维生素D类似物,与维生素D受体结合,诱导抑制甲状旁腺激素(PTH)的分泌。黑三角口服paricalcitol治疗3期或4期慢性肾病患者继发性甲状旁腺功能亢进症的效果明显优于安慰剂。在一项对三个设计良好、为期24周的试验进行的汇总分析中,与安慰剂相比,更多的特立西醇组患者的完整甲状旁腺激素水平连续两次从基线下降>/=30% (91% vs 13%)。此外,骨生化指标血清骨特异性碱性磷酸酶、血清骨钙素和尿吡啶啉的平均水平与基线相比,特立西醇组的降低幅度明显大于安慰剂组,表明骨转换减少。黑三角口服帕尔西醇耐受良好;在高钙血症、高磷血症或钙磷产物升高的发生率方面,帕尔卡醇和安慰剂接受者之间没有显著差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oral paricalcitol.

black triangle An oral formulation of paricalcitol has been developed for the prevention and treatment of secondary hyperparathyroidism in patients with stage 3 or 4 chronic kidney disease.black triangle Paricalcitol is a synthetic vitamin D analog that binds to the vitamin D receptor inducing suppression of parathyroid hormone (PTH) secretion.black triangle Oral paricalcitol was significantly more effective than placebo in treating secondary hyperparathyroidism in patients with stage 3 or 4 chronic kidney disease. In a pooled analysis of three well designed, 24-week trials, two consecutive reductions from baseline in intact PTH levels of >/=30% were achieved by significantly more paricalcitol than placebo recipients (91% vs 13%).black triangle In addition, mean levels of the biochemical bone markers serum bone-specific alkaline phosphatase, serum osteocalcin, and urinary pyridinoline were reduced from baseline to a significantly greater extent with paricalcitol than with placebo, indicating a reduction in bone turnover.black triangle Oral paricalcitol was well tolerated; there was no significant difference between paricalcitol and placebo recipients in the incidence of hypercalcemia, hyperphosphatemia, or elevated calcium-phosphorus product.

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