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Merck

Ergocalciferol and cholecalciferol in CKD.

American journal of kidney diseases : the official journal of the National Kidney Foundation (2012-05-09)
Sagar U Nigwekar, Ishir Bhan, Ravi Thadhani
RÉSUMÉ

The development of chronic kidney disease (CKD) is accompanied by a progressive decrease in the ability to produce 1,25-dihydroxyvitamin D. Pharmacological replacement with active vitamin D therefore has been a cornerstone of secondary hyperparathyroidism therapy in the end-stage renal disease population treated by long-term dialysis. Recent evidence suggests that extrarenal conversion of 25-hydroxyvitamin D to 1,25-dihydroxyvitamin D may have significant biological roles beyond those traditionally ascribed to vitamin D. Furthermore, low 25-hydroxyvitamin D levels are common in patients with all stages of CKD. This article focuses on the role of nutritional vitamin D replacement in CKD and aims to review vitamin D biology and summarize the existing literature regarding nutritional vitamin D replacement in these populations. Based on the current state of the evidence, we provide suggestions for clinical practice and address areas of uncertainty that need further research.

MATÉRIAUX
Référence du produit
Marque
Description du produit

Sigma-Aldrich
Cholécalciférol, ≥98% (HPLC)
Supelco
Cholecalciferol (D3), analytical standard
USP
Cholécalciférol, United States Pharmacopeia (USP) Reference Standard
Supelco
Cholécalciférol (vitamine D3), Pharmaceutical Secondary Standard; Certified Reference Material
Cholécalciférol, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
Cholécalciférol, meets USP testing specifications
Sigma-Aldrich
Cholécalciférol, analytical standard