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• W2038673674 endingPage "1572" @default.
• W2038673674 startingPage "1565" @default.
• W2038673674 abstract "Objective:Osteoporosis is a skeletal disorder characterized by diminished bone strength, which results in an increased risk of fracture. Currently, osteoporosis is a public health priority due to the large number of individuals affected and the detrimental effect on quality of life. Primary osteoporosis, the most common form, usually results from age-related reduction in bone mineral strength. Over time, the individual’s capacity to build bone is impaired, as the synthesis of vitamin D, the hormone responsible for calcium absorption, tends to decline. As serum calcium levels decrease, metabolic control serves to increase the removal of calcium from the skeleton to make up for the deficit. The synthesis of the ‘hormone’ vitamin D and its control therefore become central to intervention in involutional osteoporosis syndromes. In humans, plain vitamin D (cholecalciferol), also called parental or native vitamin D, is photosynthesized in the skin and then hydroxylated in the liver into the vitamin D analog calcidiol [25(OH)D3], which is hydroxylated again in the kidney into the vitamin D analog calcitriol [1,25(OH)2D3]. The advantage of administering vitamin D analogs is that the pro-drug calcidiol avoids the effect of declines in hepatic function, while calcitriol avoids the effect of declines in hepatic and kidney function. A strategy to enhance [25(OH)D3] levels to the optimal threshold of vitamin D is supplementation with the calcidiol metabolite itself. The goal of this paper is to review published studies on the efficacy of the calcidiol metabolite in increasing 25(OH)D3 serum levels and improving skeletal health parameters in humans.Methods:A library search of published papers in the area of use of calcidiol in humans from 1967 to 2013 was performed (key words: calcidiol, 25-hydroxy-vitamin D3, vitamin D supplementation, vitamin D metabolism, osteomalacia).Results and conclusion:The results of the survey made it possible to conclude that calcidiol is characterized by a number of features that make the compound ideal in conditions that require supplementation with a 25-hydroxylated metabolite." @default.
• W2038673674 created "2016-06-24" @default.
• W2038673674 creator A5015966662 @default.
• W2038673674 creator A5046313120 @default.
• W2038673674 date "2013-09-13" @default.
• W2038673674 modified "2023-09-29" @default.
• W2038673674 title "Calcidiol [25(OH)D3]: from diagnostic marker to therapeutical agent" @default.
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• W2038673674 doi "https://doi.org/10.1185/03007995.2013.838549" @default.
• W2038673674 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24020910" @default.
• W2038673674 hasPublicationYear "2013" @default.
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