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https://hdl.handle.net/20.500.12080/50966
| dc.contributor.author |
Cervero, Miguel |
|
| dc.contributor.author |
López-Wolf, Daniel |
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| dc.contributor.author |
Casado, Guiomar |
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| dc.contributor.author |
Novella-Mena, María |
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| dc.contributor.author |
Ryan-Murua, Pablo |
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| dc.contributor.author |
Taboada-Martínez, María Luisa |
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| dc.contributor.author |
Rodríguez-Mora, Sara |
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| dc.contributor.author |
Vigón, Lorena |
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| dc.contributor.author |
Coiras, Mayte |
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| dc.contributor.author |
Torres, Montserrat |
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| dc.date.accessioned |
2025-11-18T12:48:14Z |
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| dc.date.available |
2025-11-18T12:48:14Z |
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| dc.date.created |
2022 |
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| dc.identifier.uri |
https://hdl.handle.net/20.500.12080/50966 |
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| 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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