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The clinical use of vitamin D metabolites and their potential developments: A position statement from the European Society for Clinical and Economic Aspects of Osteoporosis and Osteoarthritis (ESCEO) and the International Osteoporosis Foundation (IOF)
Cianferotti, Luisella ; Cricelli, Claudio ; Kanis, John A. ; Nuti, Ranuccio ; Reginster, Jean-Yves ; Ringe, Johann D. ; Rizzoli, Rene ; Brandi, Maria Luisa
Cianferotti, Luisella
Cricelli, Claudio
Kanis, John A.
Nuti, Ranuccio
Reginster, Jean-Yves
Ringe, Johann D.
Rizzoli, Rene
Brandi, Maria Luisa
Abstract
Several compounds are produced along the complex pathways of vitamin D3 metabolism, and synthetic analogs have been generated to improve kinetics and/or vitamin D receptor activation. These metabolites display different chemical properties with respect to the parental or native vitamin D3, i.e., cholecalciferol, which has been, so far, the supplement most employed in the treatment of vitamin D inadequacy. Hydrophilic properties of vitamin D3 derivatives facilitate their intestinal absorption and their manageability in the case of intoxication because of the shorter half-life. Calcidiol is a more hydrophilic compound than parental vitamin D3. Active vitamin D analogs, capable of binding the vitamin D receptor evoking vitamin D-related biological effects, are mandatorily employed in hypoparathyroidism and kidney failure with impaired 1α-hydroxylation. They have been shown to increase BMD, supposedly ameliorating calcium absorption and/or directly affecting bone cells, although their use in these conditions is jeopardized by the development of hypercalciuria and mild hypercalcemia. Further studies are needed to assess their overall safety and effectiveness in the long-term and new intermittent regimens, especially when combined with the most effective antifracture agents.
Keywords
calcidiol, calcifediol, cholecalciferol, calcitriol, alfacalcidol, eldecalcitol
Date
2015
Type
Journal article
Journal
Endocrine
Book
Volume
50
Issue
1
Page Range
12-26
Article Number
ACU Department
Mary MacKillop Institute for Health Research
Faculty of Health Sciences
Faculty of Health Sciences
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Relation URI
Source URL
Event URL
Open Access Status
License
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Controlled
