Monthly calcifediol versus biweekly calcifediol in the treatment of patients with osteoporosis.
PDF (Português (Brasil))

Keywords

calcifediol; PTH; osteoporosis; vitamin D; makeover markers

How to Cite

Olmos , J. M. ., Arnaiz , F., Hernandez , J. L., Olmos-Martínez , J. M., & González Macías, J. (2021). Monthly calcifediol versus biweekly calcifediol in the treatment of patients with osteoporosis. Brazilian Journal of Implantology and Health Sciences, 3(6), 72–84. https://doi.org/10.36557/2674-8169.2021v3n6p72-84

Abstract

GOALS: To evaluate the serum concentrations of 25-hydroxyvitamin D, 25(OH)D, in osteoporotic patients treated for one year with calcifediol.

METHODS: We studied 156 patients with osteoporosis (23 men and 133 women) aged 71.9 ± 9.6 years who had been treated with calcifediol for at least one year. Ninety-two of them received 0.266 mg calcifediol every 15 days and he remaining 64 received the same dose once a month. Serum levels of 25(OH)D, intact PTH (iPTH), amino-terminal procollagen type I propeptide (PINP) and carboxy-terminal collagen type I telopeptide (CTX) were determined before and one year after the start of treatment .

RESULTS: With both treatment regimens, a significant increase in 25(OH)D concentration was observed (p<0.001). The percentage of patients achieving 25(OH)D levels greater than 20 and 30 ng/ml was similar with both regimens, whereas that of patients exceeding 60 ng/ml was higher with the biweekly dose (p < 0.01 ) . The iPTH concentration significantly decreased after administration of calcifediol, although on this occasion there were no differences between the two forms of treatment. Both markers, PINP and CTX, similarly decreased in patients treated with antiresorptives (p < 0.0001), without these changes being related to the calcifediol regimen.

CONCLUSIONS: A monthly administration of 0.266 mg calcifediol is adequate to achieve effective levels of vitamin D, and is also safe enough to avoid potentially harmful levels of vitamin D, so it would be preferable to the biweekly regimen in standard clinical practice.

https://doi.org/10.36557/2674-8169.2021v3n6p72-84
PDF (Português (Brasil))

References

Binkley N, Carter GD. Toward Clarity in Clinical Vitamin D Status Assessment: 25(OH)D Assay Standardization. Endocrinol Metab Clin North Am. 2017;46:885-99. [ Links ]

Dawson-Hughes B, Mithal A, Bonjour JP, Boonen S, Burckhardt P, Fuleihan GE, et al. IOF position statement vitamin D recommendations for older adults. Osteoporos Int. 2010;21:1151-4. [ Links ]

Holick MF, Binkley NC, Bischoff-Ferrari HA, Gordon CM, Hanley DA, et al. Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2011;96:1911-30. [ Links ]

Institute of Medicine (IOM). Dietary reference intakes for calcium and vitamin D. Washington, DC: National Academies Press, 2011. [ Links ]

Varsavsky M, Rozas Moreno P, Becerra Fernández A, Luque Fernández I, Quesada Gómez JM, et al.; en representación del Grupo de Trabajo de Osteoporosis y Metabolismo Mineral de la Sociedad Española de Endocrinología y Nutrición. Recomendaciones de Vitamina D para la población general. Endocrinol Diabetes Nutr. 2017;64 (Suppl 1):7-14. [ Links ]

Gómez de Tejada Romero MJ, Sosa Henríquez M, Del Pino Montes J, Jódar Gimeno E, Quesada Gómez JM, Cancelo Hidalgo MJ, et al. Documento de posición sobre las necesidades y niveles óptimos de Vitamina D. Sociedad Española de Investigación Ósea y Metabolismo Mineral (SEIOMM) y Sociedades afines. Rev Osteoporosis Metab Miner. 2011;3:53-64. [ Links ]

Zittermann A. The biphasic effect of vitamin d on the musculoskeletal and cardiovascular system. Int J Endocrinol. 2017;3206240. [ Links ]

Durup D, Jørgensen HL, Christensen J, Schwarz P, Heegaard AM, Lind B. A reverse J-shaped association of all-cause mortalitywith serum 25-hydroxyvitamin D in general practice: The CopDstudy. J Clin Endocrinol Metab. 2012;97:2644-52. [ Links ]

Cosman F, de Beur SJ, LeBoff MS, Lewiecki EM, Tanner B, Randall S, et al. Clinician’s Guide to Prevention and Treatment of Osteoporosis. Osteoporos Int. 2014;25: 2359-81. [ Links ]

González-Macías J, Del Pino-Montes J, Olmos JM, Nogués X; en nombre de la Comisión de Redacción de las Guías de Osteoporosis de la SEIOMM. Guías de práctica clínica en la osteoporosis postmenopáusica, glucocorticoidea y del varón. Sociedad Española de Investigación Ósea y del Metabolismo Mineral (3ª. Versión actualizada 2014). Rev Clin Esp. 2015;215:515-26. [ Links ]

Compston J, Cooper A, Cooper C, Gittoes N, Gregson C, Harvey N, et al; National Osteoporosis Guideline Group (NOGG). UK clinical guideline for the prevention and treatment of osteoporosis. Arch Osteoporos. 2017;12:43. [ Links ]

Díez-Pérez A, Olmos JM, Nogués X, Sosa M, Díaz-Curiel M, Pérez-Castrillón JL, et al. Risk factors for prediction of inadequate response to antiresorptives. J Bone Miner Res. 2012;27:817-24. [ Links ]

Institute of Medicine (US). Committee to review dietary reference intakes for vitamin d and calcium, dietary reference intakes for calcium and vitamin D, (2011). http://www.ncbi.nlm.nih.gov/books/NBK56070/. (Acceso el 10/02/2018). [ Links ]

Jetter A, Egli A, Dawson-Hughe B, Staehelin HB, Stoecklin E, Goessl R, et al. Pharmacokinetics of oral vitamin D(3) and calcifediol. Bone. 2014;59;14-9. [ Links ]

Shieh A, Ma C, Chun RF, Witzel S, Rafison B, Contreras HTM, et al. Effects of CholecalciferolvsCalcifediol on Total and Free 25-Hydroxyvitamin D and Parathyroid Hormone. J Clin Endocrinol Metab. 2017;102:1133-40. [ Links ]

Navarro-Valverde C, Sosa-Henríquez M, Alhambra-Expósito MR, Quesada-Gómez JM. Vitamin D3 and calcidiol are not equipotent. J Steroid Biochem Mol Biol. 2016;164:205-8. [ Links ]

Olmos JM, Hernández JL, Llorca J, Nan D, Valero C, González-Macías J. Effects of 25-Hydroxyvitamin D3 therapy on bone turnover markers and PTH levels in postmenopausal osteoporotic women treated with alendronate. J Clin Endocrinol Metab. 2012;97:4491-7. [ Links ]

Aloia JF, Talwar SA, Pollack S, Feuerman M, Yeh JK. Optimal vitamin D status and serum parathyroid hormone concentrations in African American women. Am J Clin Nutr. 2006;84:602-9. [ Links ]

Vieth R, Ladak Y, Walfish PG. Age-related changes in the 25-hydroxyvitamin D versus parathyroid hormone relationship suggest a different reason why older adults require more vitamin D. J Clin Endocrinol Metab. 2003;88:185-91. [ Links ]

Kuchuck NO, Pluijm SM, van Schoor NM, Looman CWN, Smit JH, Lips P. Relationships of serum 25-hydroxyvitamin D to bone mineral density and serum parathyroid hormone and markers of bone turnover in older persons. J Clin Endocrinol Metab. 2009;94:1244-50. [ Links ]

Nakamura K, Nashimoto M, Tsuchiya Y, Saito T, Nishiwaki T, Ueno K, et al. Threshold value of serum 25hydroxyvitamin D concentration in relation to elevated serum parathyroid hormone concentrations in elderly Japanese women. J Bone Miner Res. 2006;24:395-400. [ Links ]

Olmos JM, Hernández JL, García-Velasco P, Martínez J, Llorca J, González-Macías J. Serum 25-hydroxyvitamin D, parathyroid hormone, calcium intake, and bone mineral density in Spanish adults. Osteoporos Int. 2016;27:105-13. [ Links ]

Michaëlsson K, Baron JA, Snellman G, Gedeborg R, Byberg L, Sundström J, et al. Plasma vitamin D and mortality in older men: a community-based prospective cohort study. Am J Clin Nutr. 2010;92:841-8. [ Links ]

Smith LM, Gallagher JC, Suiter C. Medium doses of daily vitamin D decrease falls and higher doses of daily vitamin D3 increase falls: A randomized clinical trial. J Steroid Biochem Mol Biol. 2017;173:317-22. [ Links ]

Olmos, J. M., et al. "Calcifediol mensual frente a calcifediol quincenal en el tratamiento de pacientes osteoporóticos. Estudio en la vida real." Revista de Osteoporosis y Metabolismo Mineral 10.2 (2018): 89-95.

Este artigo é uma cópia com adaptação para o português do original “Olmos, J. M., et al. "Calcifediol mensual frente a calcifediol quincenal en el tratamiento de pacientes osteoporóticos. Estudio en la vida real." Revista de Osteoporosis y Metabolismo Mineral 10.2 (2018): 89-95.”25

Esta cópia com adaptação para o português teve como alteração além do idioma um pedaço do título.

Os autores da publicação original não deram endosso específico a esta cópia com adaptação para a português, a não ser a licença CCBY 4.0 disponibilizada pelo periódico que publicou o artigo original.

Este é o link da licença: https://creativecommons.org/licenses/by/4.0/

Este é o link do artigo original: https://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1889-836X2018000200005

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

Copyright (c) 2021 J M Olmos , F Arnaiz , J L Hernandez , J M Olmos-Martínez , J González Macías

Downloads

Download data is not yet available.