Publication: 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
| dc.contributor.author | Cervero, Miguel | |
| dc.contributor.author | López-Wolf, Daniel | |
| dc.contributor.author | Casado-Fernández, Guiomar | |
| dc.contributor.author | Novella-Mena, Maria | |
| dc.contributor.author | Ryan-Murua, Pablo | |
| dc.contributor.author | Taboada-Martínez, María Luisa | |
| dc.contributor.author | Rodríguez-Mora, Sara | |
| dc.contributor.author | Vigon-Hernandez, Lorena | |
| dc.contributor.author | Coiras, Mayte | |
| dc.contributor.author | Torres, Montserrat | |
| dc.contributor.funder | Fundación Universidad Alfonso X el Sabio | |
| dc.contributor.funder | Instituto de Salud Carlos III | |
| dc.contributor.funder | Ministerio de Ciencia e Innovación (España) | |
| dc.contributor.funder | Chiesi Foundation | |
| dc.contributor.funder | National Institutes of Health (Estados Unidos) | |
| dc.contributor.funder | Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF) | |
| dc.date.accessioned | 2023-01-24T11:08:33Z | |
| dc.date.available | 2023-01-24T11:08:33Z | |
| dc.date.issued | 2022-07-04 | |
| 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.description.peerreviewed | Sí | es_ES |
| dc.description.sponsorship | This work was supported by Fundación Universidad Alfonso X el Sabio (FUAX, Madrid, Spain; ID Project: 1.012.010; ID Project EQA: 925.280); the Coordinated Research Activities at the National Center of Microbiology (Instituto de Salud Carlos III) (COV20_00679) to promote an integrated response against SARS-CoV-2 in Spain (Spanish Ministry of Science and Innovation) that is coordinated by Dr. Inmaculada Casas (WHO National Influenza Center of the CNM); a generous donation provided by Chiesi España, S.A.U. (Barcelona, Spain). The work of Montserrat Torres was financed by the Coordinated Research Activities at the CNM (Instituto de Salud Carlos III) (COV20_00679). The work of Lorena Vigón was supported by a pre-doctoral grant from Instituto de Salud Carlos III (FIS PI16CIII/00034-ISCIII-FEDER). The work of Sara Rodríguez-Mora was financed by NIH grant R01AI143567. | es_ES |
| dc.format.page | 863587 | es_ES |
| dc.format.volume | 13 | es_ES |
| dc.identifier.citation | Front Pharmacol. 2022 Jul 4;13:863587. | es_ES |
| dc.identifier.doi | 10.3389/fphar.2022.863587 | es_ES |
| dc.identifier.issn | 1663-9812 | es_ES |
| dc.identifier.journal | Frontiers in pharmacology | es_ES |
| dc.identifier.pubmedID | 35860019 | es_ES |
| dc.identifier.uri | http://hdl.handle.net/20.500.12105/15432 | |
| dc.language.iso | eng | es_ES |
| dc.publisher | Frontiers Media | |
| dc.relation.projectFIS | info:eu-repo/grantAgreement/ES/COV20_00679 | es_ES |
| dc.relation.projectFIS | info:fis/Instituto de Salud Carlos III/Programa Estatal de Fomento de la Investigación Científica y Técnica de Excelencia/Subprograma Estatal de Generación de Conocimiento/ISCIII 2016 Modalidad Proyectos de Investigacion en Salud Intramurales. (2016)/PI16CIII/00034 | es_ES |
| dc.relation.publisherversion | https://doi.org/10.3389/fphar.2022.863587 | es_ES |
| dc.repisalud.centro | ISCIII::Centro Nacional de Microbiología | es_ES |
| dc.repisalud.institucion | ISCIII | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.license | Atribución 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.subject | COVID-19 | es_ES |
| dc.subject | SARS-CoV-2 | es_ES |
| dc.subject | Vitamin D3 supplementation | es_ES |
| dc.subject | Biochemical parameters | es_ES |
| dc.subject | Risk factors | 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 | research article | es_ES |
| dc.type.hasVersion | VoR | es_ES |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | dda259fe-5ac5-4b19-9249-14c375ec516b | |
| relation.isAuthorOfPublication | a78af867-a6b0-4c76-a129-d8cfa3e8c85e | |
| relation.isAuthorOfPublication | f729e106-ee5d-450a-b046-63b14e24c1a3 | |
| relation.isAuthorOfPublication | f044fea9-eb43-475b-8602-1339d49f31f4 | |
| relation.isAuthorOfPublication.latestForDiscovery | dda259fe-5ac5-4b19-9249-14c375ec516b | |
| relation.isFunderOfPublication | a6ae0db5-9c7b-4544-b685-008673740ac3 | |
| relation.isFunderOfPublication | 7d739953-4b68-4675-b5bb-387a9ab74b66 | |
| relation.isFunderOfPublication | 289dce42-6a28-4892-b0a8-c70c46cbb185 | |
| relation.isFunderOfPublication | 941a3113-c3cd-4e37-9d61-b8415006c2ac | |
| relation.isFunderOfPublication | d863b318-3e6b-4cfc-81bb-a6d112b1f86e | |
| relation.isFunderOfPublication | efa64f05-b985-4984-8f1e-5fc4ef21f502 | |
| relation.isFunderOfPublication.latestForDiscovery | a6ae0db5-9c7b-4544-b685-008673740ac3 | |
| relation.isPublisherOfPublication | 9f9fa5ea-093b-43d8-bf2c-5bd65d08a802 | |
| relation.isPublisherOfPublication.latestForDiscovery | 9f9fa5ea-093b-43d8-bf2c-5bd65d08a802 |
Files
Original bundle
1 - 1 of 1
Loading...
- Name:
- BeneficialEffectShort-TermSupplementation_2022.pdf
- Size:
- 1.49 MB
- Format:
- Adobe Portable Document Format
- Description:


