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帕立骨化醇对尿毒症血管钙化和心血管疾病的影响:超越甲状旁腺激素控制。

The Effect of Paricalcitol on Vascular Calcification and Cardiovascular Disease in Uremia: Beyond PTH Control.

作者信息

Cozzolino Mario, Mehmeti Florjan, Ciceri Paola, Volpi Elisa, Stucchi Andrea, Brenna Irene, Cusi Daniele

机构信息

Renal Division, DMCO, San Paolo Hospital, School of Medicine, University of Milan, Via A. di Rudinì 8; 20142, Milan, Italy.

出版信息

Int J Nephrol. 2011;2011:269060. doi: 10.4061/2011/269060. Epub 2011 Mar 29.

Abstract

Secondary hyperparathyroidism is a systemic disorder that associates with bone and cardiovascular disease, including arterial calcification. Treatment with calcitriol, the active form of vitamin D, reduces parathyroid hormone levels, but may result in elevations in serum calcium and phosphorus, increasing the risk of vascular calcification in dialysis patients. New vitamin D receptor activators (VDRAs) have been developed and investigated with the rationale to treat high serum PTH levels, with a reduced risk of hypercalcemia and hyperphosphatemia. Paricalcitol is a selective VDRA that suppresses PTH secretion with minimal increases on serum calcium and phosphate. Moreover, paricalcitol prevents vascular calcification in experimental models of renal failure, compared with calcitriol.

摘要

继发性甲状旁腺功能亢进是一种与骨骼和心血管疾病(包括动脉钙化)相关的全身性疾病。使用维生素D的活性形式骨化三醇进行治疗可降低甲状旁腺激素水平,但可能导致血清钙和磷升高,增加透析患者血管钙化的风险。新型维生素D受体激活剂(VDRAs)已被研发并进行研究,其目的是治疗高血清甲状旁腺激素水平,同时降低高钙血症和高磷血症的风险。帕立骨化醇是一种选择性VDRAs,它能抑制甲状旁腺激素分泌,同时使血清钙和磷酸盐的升高幅度最小。此外,与骨化三醇相比,帕立骨化醇在肾衰竭实验模型中可预防血管钙化。

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