Long-Term Treatment and Effect of Discontinuation of Calcifediol in Postmenopausal Women with Vitamin D Deficiency: A Randomized Trial

Author:

Pérez-Castrillón José Luis12,Dueñas-Laita Antonio31,Gómez-Alonso Carlos4,Jódar Esteban56,del Pino-Montes Javier78,Brandi Maria Luisa9ORCID,Cereto Castro Fernando10,Quesada-Gómez José Manuel1112,Gallego López Laura13,Olmos Martínez José Manuel141516ORCID,Alhambra Expósito María Rosa1112,Galarraga Bernat1718,González-Macías Jesús1415,Neyro José Luis1920,Bouillon Roger21ORCID,Hernández-Herrero Gonzalo22,Fernández-Hernando Nieves22,Chinchilla Sandra P.22ORCID

Affiliation:

1. School of Medicine, Universidad de Valladolid Valladolid Spain

2. Department of Internal Medicine Hospital Universitario Río Hortega Valladolid Spain

3. Clinical Toxicology Unit Hospital Universitario Río Hortega Valladolid Spain

4. Bone Metabolism Unit Hospital Universitario Central de Asturias – ISPA Oviedo Spain

5. School of Health Sciences, Universidad Europea Madrid Spain

6. Department of Endocrinology & Clinical Nutrition Hospital Universitario Quironsalud Madrid Madrid Spain

7. Department of Rheumatology Hospital Universitario de Salamanca Salamanca Spain

8. School of Medicine, Universidad de Salamanca Salamanca Spain

9. FIRMO Foundation (Fondazione Italiana Ricerca sulle Malattie dell'Osso) Florence Italy

10. Department of Internal Medicine Hospital Quirón Barcelona Barcelona Spain

11. Endocrinology and Nutrition Unit Hospital Universitario Reina Sofía Córdoba Spain

12. Physiopathology of Endocrine Vitamin D System Biotechnology and Aging Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC) Córdoba Spain

13. Department of Internal Medicine Hospital Universitario Virgen Macarena Seville Spain

14. Infection and Immunity Area Instituto de Investigación Marqués de Valdecilla (IDIVAL) Santander Spain

15. School of Medicine, Universidad de Cantabria Santander Spain

16. Internal Medicine Department Hospital Universitario Marqués de Valdecilla Santander Spain

17. Department of Medicine University of the Basque Country Leioa Spain

18. Department of Rheumatology Hospital Quirónsalud Bizkaia Erandio Spain

19. International Master on Climacteric and Menopause, Universidad de Madrid (UDIMA) Madrid Spain

20. Gynecology and Obstetrics Service Hospital Universitario Cruces Barakaldo Spain

21. Department of Chronic Diseases and Metabolism KU Leuven Leuven Belgium

22. R&D and Innovation Department Faes Farma Leioa Spain

Abstract

ABSTRACT Vitamin D plays a major role in bone health and probably also in multiple extraskeletal acute and chronic diseases. Although supplementation with calcifediol, a vitamin D metabolite, has demonstrated efficacy and safety in short-term clinical trials, its effects after long-term monthly administration have been studied less extensively. This report describes the results of a 1-year, phase III-IV, double-blind, randomized, controlled, parallel, multicenter superiority clinical trial to assess the efficacy and safety of monthly calcifediol 0.266 mg versus cholecalciferol 25,000 IU (0.625 mg) in postmenopausal women with vitamin D deficiency (25(OH)D < 20 ng/mL). A total of 303 women were randomized and 298 evaluated. Patients were randomized 1:1:1 to calcifediol 0.266 mg/month for 12 months (Group A1), calcifediol 0.266 mg/month for 4 months followed by placebo for 8 months (Group A2), and cholecalciferol 25,000 IU/month (0.625 mg/month) for 12 months (Group B). By month 4, stable 25(OH)D levels were documented with both calcifediol and cholecalciferol (intention-to-treat population): 26.8 ± 8.5 ng/mL (Group A1) and 23.1 ± 5.4 ng/mL (Group B). By month 12, 25(OH)D levels were 23.9 ± 8.0 ng/mL (Group A1) and 22.4 ± 5.5 ng/mL (Group B). When calcifediol treatment was withdrawn in Group A2, 25(OH)D levels decreased to baseline levels (28.5 ± 8.7 ng/mL at month 4 versus 14.4 ± 6.0 ng/mL at month 12). No relevant treatment-related safety issues were reported in any of the groups. The results confirm that long-term treatment with monthly calcifediol in vitamin D-deficient patients is effective and safe. The withdrawal of treatment leads to a pronounced decrease of 25(OH)D levels. Calcifediol presented a faster onset of action compared to monthly cholecalciferol. Long-term treatment produces stable and sustained 25(OH)D concentrations with no associated safety concerns. © 2023 Faes Farma SA. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

Funder

Faes Farma, S.A. and Bruno Farmaceutici S.p.A.

Publisher

Oxford University Press (OUP)

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

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