Publication:
"Effect of calcifediol treatment and best available therapy versus best available therapy on intensive care unit admission and mortality among patients hospitalized for COVID-19: A pilot randomized clinical study".

dc.contributor.authorEntrenas Castillo, Marta
dc.contributor.authorEntrenas Costa, Luis Manuel
dc.contributor.authorVaquero Barrios, Jose Manuel
dc.contributor.authorAlcala Diaz, Juan Francisco
dc.contributor.authorLopez Miranda, Jose
dc.contributor.authorBouillon, Roger
dc.contributor.authorQuesada Gomez, Jose Manuel
dc.contributor.funderConsejería de Salud y Familia
dc.contributor.funderFundación Progreso y Salud
dc.contributor.funderFundación para la Investigación Biomédica de Córdoba (FIBICO)
dc.date.accessioned2023-02-09T09:39:40Z
dc.date.available2023-02-09T09:39:40Z
dc.date.issued2020-08-24
dc.description.abstractThe vitamin D endocrine system may have a variety of actions on cells and tissues involved in COVID-19 progression especially by decreasing the Acute Respiratory Distress Syndrome. Calcifediol can rapidly increase serum 25OHD concentration. We therefore evaluated the effect of calcifediol treatment, on Intensive Care Unit Admission and Mortality rate among Spanish patients hospitalized for COVID-19. Parallel pilot randomized open label, double-masked clinical trial. University hospital setting (Reina Sofia University Hospital, Córdoba Spain.) PARTICIPANTS: 76 consecutive patients hospitalized with COVID-19 infection, clinical picture of acute respiratory infection, confirmed by a radiographic pattern of viral pneumonia and by a positive SARS-CoV-2 PCR with CURB65 severity scale (recommending hospital admission in case of total score > 1). All hospitalized patients received as best available therapy the same standard care, (per hospital protocol), of a combination of hydroxychloroquine (400 mg every 12 h on the first day, and 200 mg every 12 h for the following 5 days), azithromycin (500 mg orally for 5 days. Eligible patients were allocated at a 2 calcifediol:1 no calcifediol ratio through electronic randomization on the day of admission to take oral calcifediol (0.532 mg), or not. Patients in the calcifediol treatment group continued with oral calcifediol (0.266 mg) on day 3 and 7, and then weekly until discharge or ICU admission. Outcomes of effectiveness included rate of ICU admission and deaths. Of 50 patients treated with calcifediol, one required admission to the ICU (2%), while of 26 untreated patients, 13 required admission (50 %) p value X2 Fischer test p Our pilot study demonstrated that administration of a high dose of Calcifediol or 25-hydroxyvitamin D, a main metabolite of vitamin D endocrine system, significantly reduced the need for ICU treatment of patients requiring hospitalization due to proven COVID-19. Calcifediol seems to be able to reduce severity of the disease, but larger trials with groups properly matched will be required to show a definitive answer.
dc.description.sponsorshipJose Manuel Quesada Gomez y Luis Manuel Entrenas costa had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. We acknowledge the dedication, commitment, and sacrifice of the staff, and personnel in our institution through the Covid-19 crisis and the suffering and loss of our patients as well as in their families and our Community. We appreciate the statistical work of Ipek Guler, and Carmen Molina. We are grateful to COVID-011-2020 “Programa de Investigacion ´ clínica en COVID-19 de Andalucía”. Consejería de Salud y Familia. “Fundación Progreso y Salud” and “Fundación para la Investigacion ´ Biomédica de Cordoba ´ ” (FIBICO). Andalucía. Spain.
dc.description.versionSi
dc.identifier.citationEntrenas Castillo M, Entrenas Costa LM, Vaquero Barrios JM, Alcalá Díaz JF, López Miranda J, Bouillon R, et al. "Effect of calcifediol treatment and best available therapy versus best available therapy on intensive care unit admission and mortality among patients hospitalized for COVID-19: A pilot randomized clinical study". J Steroid Biochem Mol Biol. 2020 Oct;203:105751
dc.identifier.doi10.1016/j.jsbmb.2020.105751
dc.identifier.essn1879-1220
dc.identifier.pmcPMC7456194
dc.identifier.pmid32871238
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7456194/pdf
dc.identifier.unpaywallURLhttps://doi.org/10.1016/j.jsbmb.2020.105751
dc.identifier.urihttp://hdl.handle.net/10668/16186
dc.journal.titleThe Journal of steroid biochemistry and molecular biology
dc.journal.titleabbreviationJ Steroid Biochem Mol Biol
dc.language.isoen
dc.organizationHospital Universitario Reina Sofía
dc.organizationInstituto Maimónides de Investigación Biomédica de Córdoba-IMIBIC
dc.page.number7
dc.pubmedtypeComparative Study
dc.pubmedtypeJournal Article
dc.pubmedtypeRandomized Controlled Trial
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject1α, 25(OH)2D or 1α, 25-dihydroxyvitamin D or calcitriol
dc.subjectAcute respiratory distress syndrome (ARDS)
dc.subjectCOVID-19
dc.subjectCalcifediol or 25-hydroxyvitamin D3
dc.subjectCathelicidin peptide
dc.subjectChloroquine
dc.subjectCovidiol
dc.subjectCuboidal alveolar coating cells type II
dc.subjectCytokine/Chemokine storm
dc.subjectDefensins
dc.subjectHydroxychloroquine
dc.subjectHypercoagulability
dc.subjectNeutrophil activity
dc.subjectRenin-angiotensin system
dc.subjectSARS-CoV-2
dc.subjectTLR co-receptor CD14
dc.subjectVitamin D
dc.subjectVitamin D endocrine system
dc.subjectVitamin D receptor
dc.subjectVitamin D3 or cholecalciferol
dc.subject.decsConservadores de la densidad ósea
dc.subject.decsHospitalización
dc.subject.decsInfecciones por coronavirus
dc.subject.decsNeumonía viral
dc.subject.decsPandemias
dc.subject.decsPronóstico
dc.subject.decsProyectos piloto
dc.subject.meshBetacoronavirus
dc.subject.meshBone density conservation agents
dc.subject.meshCOVID-19
dc.subject.meshCalcifediol
dc.subject.meshCoronavirus infections
dc.subject.meshDouble-blind method
dc.subject.meshFemale
dc.subject.meshHospitalization
dc.subject.meshHumans
dc.subject.meshIntensive care units
dc.subject.meshMale
dc.subject.meshMiddle aged
dc.subject.meshPandemics
dc.subject.meshPilot projects
dc.subject.meshPneumonia, viral
dc.subject.meshPrognosis
dc.subject.meshSARS-CoV-2
dc.title"Effect of calcifediol treatment and best available therapy versus best available therapy on intensive care unit admission and mortality among patients hospitalized for COVID-19: A pilot randomized clinical study".
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number203
dspace.entity.typePublication

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