Analgesics
Antiandrogens
Azvudine
Bromhexine
Budesonide
Colchicine
Conv. Plasma
Curcumin
Famotidine
Favipiravir
Fluvoxamine
Hydroxychlor..
Ivermectin
Lifestyle
Melatonin
Metformin
Minerals
Molnupiravir
Monoclonals
Naso/orophar..
Nigella Sativa
Nitazoxanide
Paxlovid
Quercetin
Remdesivir
Thermotherapy
Vitamins
More

Other
Feedback
Home
Top
Abstract
All vitamin D studies
Meta analysis
 
Feedback
Home
next
study
previous
study
c19early.org COVID-19 treatment researchVitamin DVitamin D (more..)
Melatonin Meta
Metformin Meta
Azvudine Meta
Bromhexine Meta Molnupiravir Meta
Budesonide Meta
Colchicine Meta
Conv. Plasma Meta Nigella Sativa Meta
Curcumin Meta Nitazoxanide Meta
Famotidine Meta Paxlovid Meta
Favipiravir Meta Quercetin Meta
Fluvoxamine Meta Remdesivir Meta
Hydroxychlor.. Meta Thermotherapy Meta
Ivermectin Meta

All Studies   Meta Analysis    Recent:   

Vitamin D deficiency in critically ill COVID-19 ARDS patients

Notz et al., Clinical Nutrition, doi:10.1016/j.clnu.2021.03.001
Mar 2021  
  Post
  Facebook
Share
  Source   PDF   All Studies   Meta AnalysisMeta
Vitamin D for COVID-19
8th treatment shown to reduce risk in October 2020
 
*, now known with p < 0.00000000001 from 120 studies, recognized in 8 countries.
No treatment is 100% effective. Protocols combine complementary and synergistic treatments. * >10% efficacy in meta analysis with ≥3 clinical studies.
4,000+ studies for 60+ treatments. c19early.org
Retrospective 26 ICU patients showing that the majority of patients had vitamin D deficiency. There was no statistically significant association of 25-hydroxyvitamin D status and clinical course, however low levels of 1,25-dihydroxyvitamin D were associated with prolonged mechanical ventilation and a worse APACHE II score. Clinical outcomes based on baseline vitamin D status are not provided.
Notz et al., 7 Mar 2021, peer-reviewed, 12 authors.
This PaperVitamin DAll
Vitamin D deficiency in critically ill COVID-19 ARDS patients
Quirin Notz, Johannes Herrmann, Tobias Schlesinger, Peter Kranke, Magdalena Sitter, Philipp Helmer, Jan Stumpner, Daniel Roeder, Karin Amrein, Christian Stoppe, Christopher Lotz, Patrick Meybohm
Clinical Nutrition, doi:10.1016/j.clnu.2021.03.001
Background & aims: Vitamin D's pleiotropic effects include immune modulation, and its supplementation has been shown to prevent respiratory tract infections. The effectivity of vitamin D as a therapeutic intervention in critical illness remains less defined. The current study analyzed clinical and immunologic effects of vitamin D levels in patients suffering from coronavirus disease 2019 (COVID-19) induced acute respiratory distress syndrome (ARDS). Methods: This was a single-center retrospective study in patients receiving intensive care with a confirmed SARS-CoV-2 infection and COVID-19 ARDS. 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D serum levels, pro-and anti-inflammatory cytokines and immune cell subsets were measured on admission as well as after 10e15 days. Clinical parameters were extracted from the patient data management system. Standard operating procedures included the daily administration of vitamin D 3 via enteral feeding. Results: A total of 39 patients with COVID-19 ARDS were eligible, of which 26 were included in this study as data on vitamin D status was available. 96% suffered from severe COVID-19 ARDS. All patients without prior vitamin D supplementation (n ¼ 22) had deficient serum levels of 25-hydroxyvitamin D. Vitamin D supplementation resulted in higher serum levels of 25-hydroxyvitamin D but not did not increase 1,25dihydroxyvitamin D levels after 10e15 days. Clinical parameters did not differ between patients with sufficient or deficient levels of 25-hydroxyvitamin D. Only circulating plasmablasts were higher in patients with 25-hydroxyvitamin D levels !30 ng/ml (p ¼ 0.029). Patients with 1,25-dihydroxyvitamin D levels below 20 pg/ml required longer mechanical ventilation (p ¼ 0.045) and had a worse acute physiology and chronic health evaluation (APACHE) II score (p ¼ 0.048). Conclusion: The vast majority of COVID-19 ARDS patients had vitamin D deficiency. 25-hydroxyvitamin D status was not related to changes in clinical course, whereas low levels of 1,25-dihydroxyvitamin D were associated with prolonged mechanical ventilation and a worse APACHE II score.
Author contributions QN, PK, CL, and PM contributed substantially to the conception and design of the study, the acquisition, analysis, interpretation of the data and drafted the article. CS contributed substantially to the conception and design of the study, interpretation of the data and revised the manuscript. JH, TS, MS, PH contributed substantially to the acquisition of the data. JS, DR, KA contributed substantially to the interpretation of the data and critical revision of the article. All authors provided final approval of the version submitted for publication. Conflict of interest None.
References
Amrein, Schnedl, Holl, Riedl, Christopher et al., Effect of high-dose vitamin D3 on hospital length of stay in critically ill patients with vitamin D deficiency: the VITdAL-ICU randomized clinical trial, Jama
Amrein, Zajic, Schnedl, Waltensdorfer, Fruhwald et al., Vitamin D status and its association with season, hospital and sepsis mortality in critical illness, Crit Care
Anderson, Do, Toh, Hoe, Reitsma et al., Vitamin D induces differential effects on inflammatory responses during bacterial and/or viral stimulation of human peripheral blood mononuclear cells, Front Immunol
Belderbos, Houben, Wilbrink, Lentjes, Bloemen et al., Cord blood vitamin D deficiency is associated with respiratory syncytial virus bronchiolitis, Pediatrics
Berry, Hesketh, Power, Hypp€ Onen E, Vitamin D status has a linear association with seasonal infections and lung function in British adults, Br J Nutr
Corman, Landt, Kaiser, Molenkamp, Meijer et al., Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR, Euro Surveill
Enez-Sousa, Martínez, Medrano, Andez-Rodríguez, Resino, Vitamin D in human immunodeficiency virus infection: influence on immunity and disease, Front Immunol
Fig, None
Fink, Origin and function of circulating plasmablasts during acute viral infections, Front Immunol
Fitch, Becker, Hayglass, Vitamin D [1,25(OH)2D3] differentially regulates human innate cytokine responses to bacterial versus viral pattern recognition receptor stimuli, J Immunol
Ginde, Brower, Caterino, Finck, Banner-Goodspeed et al., Early high-dose vitamin D(3) for critically ill, vitamin Ddeficient patients, N Engl J Med
Ho, Celis-Morales, Gray, Katikireddi, Niedzwiedz et al., Modifiable and non-modifiable risk factors for COVID-19, and comparison to risk factors for influenza and pneumonia: results from a UK Biobank prospective cohort study, BMJ Open
Holick, Binkley, Bischoff-Ferrari, Gordon, Hanley et al., Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline, J Clin Endocrinol Metabol
Holick, Vitamin D deficiency, N Engl J Med
Khammissa, Fourie, Motswaledi, Ballyram, Lemmer et al., The biological activities of vitamin D and its receptor in relation to calcium and bone homeostasis, cancer, immune and cardiovascular systems, skin biology, and oral health, BioMed Res Int
Kolls, Ray, Wenzel, High-dose vitamin D3 for critically ill vitamin Ddeficient patients, N Engl J Med
Langlois, Szwec, 'aragon, Heyland, Manzanares, Vitamin D supplementation in the critically ill: a systematic review and meta-analysis, Clin Nutr
Leaf, Raed, Donnino, Ginde, Waikar, Randomized controlled trial of calcitriol in severe sepsis, Am J Respir Crit Care Med
Maloney, Almarines, Goolkasian, Vitamin D levels and monospot tests in military personnel with acute pharyngitis: a retrospective chart review, PloS One
Martineau, Jolliffe, Hooper, Greenberg, Aloia et al., Vitamin D supplementation to prevent acute respiratory tract infections: systematic review and meta-analysis of individual participant data, BMJ
Martucci, Mcnally, Parekh, Zajic, Tuzzolino et al., Trying to identify who may benefit most from future vitamin D intervention trials: a post hoc analysis from the VITDAL-ICU study excluding the early deaths, Crit Care
Mcnally, Nama, 'hearn, Sampson, Amrein et al., Vitamin D deficiency in critically ill children: a systematic review and meta-analysis, Crit Care
Morbach, Eichhorn, Liese, Girschick, Reference values for B cell subpopulations from infancy to adulthood, Clin Exp Immunol
Ney, Heyland, Amrein, Marx, Grottke et al., The relevance of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D concentration for postoperative infections and postoperative organ dysfunctions in cardiac surgery patients: the eVIDenCe study, Clin Nutr
Palacios, Gonzalez, Is vitamin D deficiency a major global public health problem?, J Steroid Biochem Mol Biol
Raisi-Estabragh, Mccracken, Bethell, Cooper, Cooper et al., Greater risk of severe COVID-19 in Black, Asian and Minority Ethnic populations is not explained by cardiometabolic, socioeconomic or behavioural factors, or by 25(OH)-vitamin D status: study of 1326 cases from the UK Biobank, J Public Health (Oxf)
Ranieri, Rubenfeld, Thompson, Ferguson, Acute respiratory distress syndrome: the Berlin Definition, Jama
Sundaram, Coleman, Vitamin D and influenza, Adv Nutr
Tang, Jackson, Walsh, Greeves, Fraser, The dynamic relationships between the active and catabolic vitamin D metabolites, their ratios, and associations with PTH, Sci Rep
Telcian, Zdrenghea, Edwards, Laza-Stanca, Mallia et al., Vitamin D increases the antiviral activity of bronchial epithelial cells in vitro, Antivir Res
Vandenbroucke, Elm, Altman, Gøtzsche, Mulrow et al., Strengthening the reporting of observational studies in epidemiology (STROBE): explanation and elaboration, Ann Intern Med
Warnatz, Schlesier, Flow cytometric phenotyping of common variable immunodeficiency, Cytometry B Clin Cytometry
Zaidan, Wang, High-dose vitamin D3 for critically ill vitamin D-deficient patients, N Engl J Med
Late treatment
is less effective
Please send us corrections, updates, or comments. c19early involves the extraction of 100,000+ datapoints from thousands of papers. Community updates help ensure high accuracy. Treatments and other interventions are complementary. All practical, effective, and safe means should be used based on risk/benefit analysis. No treatment or intervention is 100% available and effective for all current and future variants. We do not provide medical advice. Before taking any medication, consult a qualified physician who can provide personalized advice and details of risks and benefits based on your medical history and situation. FLCCC and WCH provide treatment protocols.
  or use drag and drop   
Submit