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J Steroid Biochem Mol Biol. 2014 Oct;144 Pt A:207-14. doi: 10.1016/j.jsbmb.2013.10.004. Epub 2013 Oct 12.
2
Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline.维生素 D 缺乏的评估、治疗和预防:内分泌学会临床实践指南。
J Clin Endocrinol Metab. 2011 Jul;96(7):1911-30. doi: 10.1210/jc.2011-0385. Epub 2011 Jun 6.
3
Clinical Significance of FGF-23 in Patients with CKD.成纤维细胞生长因子-23(FGF-23)在慢性肾脏病患者中的临床意义
Int J Nephrol. 2011;2011:364890. doi: 10.4061/2011/364890. Epub 2011 Apr 26.
4
Fibroblast growth factor 23 is elevated before parathyroid hormone and phosphate in chronic kidney disease.成纤维细胞生长因子 23 在慢性肾脏病中比甲状旁腺激素和磷酸盐更早升高。
Kidney Int. 2011 Jun;79(12):1370-8. doi: 10.1038/ki.2011.47. Epub 2011 Mar 9.
5
Vitamin D: the iceberg nutrient.维生素 D:冰山一角的营养物质。
J Ren Nutr. 2011 Mar;21(2):134-9. doi: 10.1053/j.jrn.2010.09.002. Epub 2011 Jan 15.
6
Why dialysis patients need combination therapy with both cholecalciferol and a calcitriol analogs.为什么透析患者需要胆钙化醇和骨化三醇类似物联合治疗。
Semin Dial. 2010 May-Jun;23(3):239-43. doi: 10.1111/j.1525-139X.2010.00722.x. Epub 2010 May 10.
7
Cholecalciferol supplementation in hemodialysis patients: effects on mineral metabolism, inflammation, and cardiac dimension parameters.骨化三醇补充治疗血液透析患者:对矿物质代谢、炎症和心脏结构参数的影响。
Clin J Am Soc Nephrol. 2010 May;5(5):905-11. doi: 10.2215/CJN.06510909. Epub 2010 Mar 4.
8
Cholecalciferol supplementation alters calcitriol-responsive monocyte proteins and decreases inflammatory cytokines in ESRD.胆钙化醇补充改变了 ESRD 患者中钙三醇反应性单核细胞蛋白,并降低了炎症细胞因子。
J Am Soc Nephrol. 2010 Feb;21(2):353-61. doi: 10.1681/ASN.2009040451. Epub 2009 Dec 10.
9
KDIGO clinical practice guideline for the diagnosis, evaluation, prevention, and treatment of Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD).改善全球肾脏病预后组织(KDIGO)慢性肾脏病-矿物质和骨异常(CKD-MBD)诊断、评估、预防及治疗临床实践指南。
Kidney Int Suppl. 2009 Aug(113):S1-130. doi: 10.1038/ki.2009.188.
10
Monthly cholecalciferol administration in haemodialysis patients: a simple and efficient strategy for vitamin D supplementation.血液透析患者每月给予胆钙化醇治疗:一种简单有效的维生素 D 补充策略。
Nephrol Dial Transplant. 2009 Dec;24(12):3799-805. doi: 10.1093/ndt/gfp370. Epub 2009 Jul 21.

血液透析患者补充胆钙化醇后 25-羟维生素 D 的反应。

25-Hydroxyvitamin D response to cholecalciferol supplementation in hemodialysis.

机构信息

Osteoporosis Research Center, Creighton University, Omaha, Nebraska 68131, USA.

出版信息

Clin J Am Soc Nephrol. 2012 Sep;7(9):1428-34. doi: 10.2215/CJN.12761211. Epub 2012 Jul 12.

DOI:10.2215/CJN.12761211
PMID:22798536
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3430950/
Abstract

BACKGROUND AND OBJECTIVES

Recent understanding of extrarenal production of calcitriol has led to the exploration of native vitamin D treatment in dialysis patients. This paper reports the pharmacokinetics of 25-hydroxyvitamin D response to 10,333 IU cholecalciferol given weekly in subjects on chronic dialysis.

DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: This randomized, double-blind, placebo-controlled trial of 15 weeks of oral cholecalciferol in subjects with stage 5 CKD requiring maintenance hemodialysis was conducted from November of 2007 to March of 2010. The time course of serum 25-hydroxyvitamin D was measured over the course of treatment. Additionally, blood was drawn at baseline and last visit for calcium, phosphorus, calcitriol, and parathyroid hormone levels.

RESULTS

The median (interquartile range) baseline 25-hydroxyvitamin D level was 13.3 (11.1-16.2) ng/ml for the treatment group and 15.2 (10.7-19.9) ng/ml for the placebo group. 25-hydroxyvitamin D steady state levels rose by 23.6 (19.2-29.9) ng/ml in the treatment group, and there was no change in the placebo group. Calcitriol levels also increased significantly in the treatment group. There were no significant changes in levels of calcium, albumin, phosphorus, and parathyroid hormone in either group.

CONCLUSIONS

Cholecalciferol (10,333 IU) given weekly in patients on chronic hemodialysis produces a steady state in 25-hydroxyvitamin D of approximately 24 ng/ml.

摘要

背景和目的

最近对肾脏外源性 1,25-二羟维生素 D3(1,25-(OH)2D3)生成的认识,促使人们探索对透析患者进行内源性维生素 D 治疗。本文报告了在慢性血液透析患者中每周给予 10,333IU 胆钙化醇治疗后,25-羟维生素 D 反应的药代动力学。

设计、设置、参与者和测量:2007 年 11 月至 2010 年 3 月,对 15 名需要维持性血液透析的 5 期慢性肾脏病(CKD)患者进行了为期 15 周的口服胆钙化醇随机、双盲、安慰剂对照试验。在治疗过程中测量了血清 25-羟维生素 D 的时间过程。此外,在基线和最后一次就诊时采集血液,以测量钙、磷、1,25-(OH)2D3 和甲状旁腺激素水平。

结果

治疗组的中位(四分位距)基线 25-羟维生素 D 水平为 13.3(11.1-16.2)ng/ml,安慰剂组为 15.2(10.7-19.9)ng/ml。治疗组 25-羟维生素 D 稳态水平升高 23.6(19.2-29.9)ng/ml,而安慰剂组没有变化。治疗组 1,25-(OH)2D3 水平也显著升高。两组血钙、白蛋白、磷和甲状旁腺激素水平均无显著变化。

结论

在慢性血液透析患者中每周给予 10,333IU 胆钙化醇可使 25-羟维生素 D 达到约 24ng/ml 的稳态水平。