| Nutrients | |
| A Randomized, Double-Blind, Parallel Study to Evaluate the Dose-Response of Three Different Vitamin D Treatment Schemes on the 25-Hydroxyvitamin D Serum Concentration in Patients with Vitamin D Deficiency | |
| Marie-Louise Schleck5  Jean-Claude Souberbielle2  Bernard Jandrain4  Stéphanie Da Silva1  Sophie De Niet1  Francis Vanderbist1  André Scheen3  | |
| [1] Clinical Department, Laboratoires SMB SA, Brussels 1080, Belgium; E-Mails:;Laboratoire d’Explorations fonctionnelles, Hôpital Necker-Enfants malades, Paris 75015, France; E-Mail:;Division of Diabetes, Nutrition and Metabolic Disorders, CHU Sart Tilman, University of Liège, Liège B-4000, Belgium; E-Mail:;Department of Clinical Pharmacology, ATC SA, Liège B-4000, Belgium; E-Mail:;Department of Clinical Chemistry, University of Liège, CHU Sart-Tilman, Liège B-4000, Belgium; E-Mail: | |
| 关键词: vitamin D; randomized double-blind trial; safety; | |
| DOI : 10.3390/nu7075227 | |
| 来源: mdpi | |
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【 摘 要 】
Many people worldwide are vitamin D (VTD) deficient or insufficient, and there is still no consensus on the dose of VTD that should be administered to achieve a 25(OH)D concentration of 20 or 30 ng/mL. In this study, we aimed to determine an adapted supplementation of VTD able to quickly and safely increase the vitamin D status of healthy adults with low 25(OH)D. One hundred and fifty (150) subjects were randomized into three groups, each to receive, orally, a loading dose of 50,000, 100,000 or 200,000 IU of VTD3 at Week 0, followed by 25,000, 50,000 or 100,000 IU at Week 4 and Week 8. Whereas 25(OH)D baseline values were not different between groups (
【 授权许可】
CC BY
© 2015 by the authors; licensee MDPI, Basel, Switzerland.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO202003190009840ZK.pdf | 190KB |
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