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Beneficial Effect of Short-Term Supplementation of High Dose of Vitamin D3 in Hospitalized Patients With COVID-19: A Multicenter, Single-Blinded, Prospective Randomized Pilot Clinical Trial

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https://hdl.handle.net/20.500.12080/50966
dc.contributor.author Cervero, Miguel
dc.contributor.author López-Wolf, Daniel
dc.contributor.author Casado, Guiomar
dc.contributor.author Novella-Mena, María
dc.contributor.author Ryan-Murua, Pablo
dc.contributor.author Taboada-Martínez, María Luisa
dc.contributor.author Rodríguez-Mora, Sara
dc.contributor.author Vigón, Lorena
dc.contributor.author Coiras, Mayte
dc.contributor.author Torres, Montserrat
dc.date.accessioned 2025-11-18T12:48:14Z
dc.date.available 2025-11-18T12:48:14Z
dc.date.created 2022
dc.identifier.uri https://hdl.handle.net/20.500.12080/50966
dc.description.abstract There is now sufficient evidence to support that vitamin D deficiency may predispose to SARS-CoV-2 infection and increase COVID-19 severity and mortality. It has been suggested that vitamin D3 supplementation may be used prophylactically as an affordable and safe strategy that could be added to the existing COVID-19 standard treatment. This multicenter, single-blinded, prospective randomized pilot clinical trial aimed to evaluate the safety, tolerability, and effectiveness of 10,000 IU/day in comparison with 2000 IU/day of cholecalciferol supplementation for 14 days to reduce the duration and severity of COVID-19 in 85 hospitalized individuals. The median age of the participants was 65 years (Interquartile range (IQR): 53¿74), most of them (71%) were men and the mean baseline of 25-hydroxyvitamin D (25(OH)D) in serum was 15 ng/ml (standard deviation (SD):6). After 14 days of supplementation, serum 25(OH)D levels were significantly increased in the group who received 10,000IU/day (p < 0.0001) (n = 44) in comparison with the 2,000IU/day group (n = 41), especially in overweight and obese participants, and the higher dose was well tolerated. A fraction of the individuals in our cohort (10/85) developed acute respiratory distress syndrome (ARDS). The median length of hospital stay in these patients with ARDS was significantly different in the participants assigned to the 10,000IU/day group (n = 4; 7 days; IQR: 4¿13) and the 2,000IU/day group (n = 6; 27 days; IQR: 12¿45) (p = 0.04). Moreover, the inspired oxygen fraction was reduced 7.6-fold in the high dose group (p = 0.049). In terms of blood parameters, we did not identify overall significant improvements, although the platelet count showed a modest but significant difference in those patients who were supplemented with the higher dose (p = 0.0492). In conclusion, the administration of 10,000IU/day of vitamin D3 for 14 days in association with the standard clinical care during hospitalization for COVID-19 was safe, tolerable, and beneficial, thereby helping to improve the prognosis during the recovery process. es_ES
dc.format application/pdf es_ES
dc.language eng es_ES
dc.publisher Frontiers es_ES
dc.rights CC-BY es_ES
dc.rights.uri http://creativecommons.org/licenses/by/4.0/deed.es es_ES
dc.source Frontiers in Pharmacology es_ES
dc.title Beneficial Effect of Short-Term Supplementation of High Dose of Vitamin D3 in Hospitalized Patients With COVID-19: A Multicenter, Single-Blinded, Prospective Randomized Pilot Clinical Trial es_ES
dc.type Artículo es_ES
dc.description.curso 2022 es_ES
dc.rights.accessrights info:eu-repo/semantics/openAccess es_ES
dc.identifier.dl 2022
dc.identifier.location N/A es_ES


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