» Articles » PMID: 22461169

Biological Effects of Various Regimes of 25-hydroxyvitamin D3 (calcidiol) Administration on Bone Mineral Metabolism in Postmenopausal Women

Overview
Date 2012 Mar 31
PMID 22461169
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction. It is evident from several studies that vitamin D inadequacy is widespread among women with osteoporosis across all continents regardless of season or latitude, with similar prevalence in patients treated for osteoporosis and in untreated women. These results underscore a need to improve physician and patient awareness of the importance of adequate vitamin D supplementation in postmenopausal women with osteoporosis.Materials and Methods. As the daily administration of vitamin D combined with 1 gr calcium is hampered by an insufficient patient adherence, we performed a longitudinal study in 90 randomly recruited postmenopausal women aged 65-75 years with inadequate calcium intake and circulating levels of 25-hydroxyvitamin D3 (lower than 30 ng/mL). The prevalence of secondary hyperparathyroidism (parathyroid hormone > 65 pg/mL) was 36% in the all population. The possible repercussion of oral single weekly or monthly calcidiol administration on phospho-calcium metabolism was observed after three months treatment (from April through July) with 500 mg calcium daily and with three different therapeutic regimens of calcidiol (Group I: 25 drops weekly; Group II: 50 drops monthly; and Group III: 100 drops monthly). The general baseline characteristics of the three groups were superimposable. We measured fasting morning serum 25-hydroxyvitamin D3, parathyroid hormone, calcium, phosphate, bone alkaline phosphatase, urinary deoxypyridinoline, and 24hr-calcium, - phosphate, and - creatinine.Results. The adherence to the weekly calcidiol treatment was over 80% in 90% of the patients. All three therapeutic regimens of calcidiol led to normalization of 25-hydroxyvitamin D3 after 3 months, yet with a significantly higher potency (P >0.01) of regimens I and III, when compared to Group II. Also the decrease of circulating levels of parathyroid hormone was significantly higher (P < 0.001) in Groups I and III versus Group II. No biochemically and clinically relevant adverse effects were observed at the end of the 90-day follow-up.ConclusionsIn postmenopausal women with inadequate circulating levels of 25-hydroxyvitamin D3, calcium and pulsed calcidiol supplementation normalized 25-hydroxyvitamin D3 levels and reduced circulating parathyroid hormone levels.

Citing Articles

Sociodemographic, Anthropometric, Body Composition, Nutritional, and Biochemical Factors Influenced by Age in a Postmenopausal Population: A Cross-Sectional Study.

Vazquez-Lorente H, Herrera-Quintana L, Molina-Lopez J, Lopez-Gonzalez B, Planells E Metabolites. 2023; 13(1).

PMID: 36677003 PMC: 9864446. DOI: 10.3390/metabo13010078.


Evolving Role of Vitamin D in Immune-Mediated Disease and Its Implications in Autoimmune Hepatitis.

Czaja A, Montano-Loza A Dig Dis Sci. 2018; 64(2):324-344.

PMID: 30370494 DOI: 10.1007/s10620-018-5351-6.


25(OH)D3-enriched or fortified foods are more efficient at tackling inadequate vitamin D status than vitamin D3.

Guo J, Lovegrove J, Givens D Proc Nutr Soc. 2017; 77(3):282-291.

PMID: 29173203 PMC: 6088524. DOI: 10.1017/S0029665117004062.


Indications on the use of vitamin D and vitamin D metabolites in clinical phenotypes.

Brandi M Clin Cases Miner Bone Metab. 2012; 7(3):243-50.

PMID: 22460535 PMC: 3213838.

References
1.
Vieth R . Why the optimal requirement for Vitamin D3 is probably much higher than what is officially recommended for adults. J Steroid Biochem Mol Biol. 2004; 89-90(1-5):575-9. DOI: 10.1016/j.jsbmb.2004.03.038. View

2.
Davey D . Vitamin D and its analogues and the prevention and treatment of osteoporosis. S Afr Med J. 1997; 87(4):423-5. View

3.
Rao D . Perspective on assessment of vitamin D nutrition. J Clin Densitom. 2000; 2(4):457-64. DOI: 10.1016/s1094-6950(06)60411-3. View

4.
UTIGER R . The need for more vitamin D. N Engl J Med. 1998; 338(12):828-9. DOI: 10.1056/NEJM199803193381209. View

5.
Kuchuk N, van Schoor N, Pluijm S, Chines A, Lips P . Vitamin D status, parathyroid function, bone turnover, and BMD in postmenopausal women with osteoporosis: global perspective. J Bone Miner Res. 2008; 24(4):693-701. DOI: 10.1359/jbmr.081209. View