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      Vitamin C levels in patients with SARS-CoV-2-associated acute respiratory distress syndrome

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          Abstract

          Vitamin C is an antioxidant with anti-inflammatory and immune-supportive properties. Its levels are decreased in patients with sepsis-related acute respiratory distress syndrome (ARDS). Moreover, a significant number of patients with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) disease developed ARDS [1]. Therefore, we hypothesized that ARDS coronavirus disease 2019 (COVID-19) patients may present vitamin C deficiency. Plasma vitamin C levels in a population of adult ICU patients COVID-19 who met ARDS criteria according to the Berlin definition [2] were prospectively measured. The study was approved by the local Clinical Research Ethics Committee (PR (AG)270/2020). Main characteristics of the population included are presented in Table 1. None of the patients included presented shock or sepsis on admission. Equally, no bacterial co-infection during their ICU course was documented. All patients survived. Vitamin C was determined by high-performance liquid chromatography with photodiode detector (detection limit 1.5 mg/L). Vitamin C reference values in general population used to be above 5 mg/L. Seventeen patients (94.4%) had undetectable vitamin C levels and 1 patient had low levels (2.4 mg/L). Table 1 Clinical characteristics of the COVID-19 patients included. We have included the worst PF and highest PEEP. Results of continuous variables are expressed as mean and standard deviation or median and interquartile range as appropriate. Categorical variables are expressed as frequency (percentage). SOFA sequential organ failure assessment, APACHE II Acute Physiology and Chronic Health disease Classification System II, ICU intensive care unit, PF PaO2/FiO2 ratio, PEEP positive end-expiratory pressure, AKI acute kidney injury, CRRT continuous renal replacement therapy, LMWH low-molecular-weight heparin Clinical characteristics COVID-19 ARDS (n = 18) Age (mean, standard deviation, years) 59 ± 9 Male (n, %) 7 (38) SOFA score (median, interquartile range, points) 4 (1) APACHE II score (mean, standard deviation, points) 16.2 ± 1.6 Interval between ICU admission and blood samples extraction for vitamin C measurement (mean, standard deviation, days) 17.5 ± 1.7 Interval between intubation and blood samples extraction for vitamin C measurement (mean, standard deviation, days) 17.5 ± 1.7 ARDS-related variables  PaO2/FIO2 at the time of vitamin C measurement (mean, standard deviation, mmHg) 94.4 ± 5.9  PEEP (cmH2O) at the time of vitamin C measurement (median, interquartile range, points) 13.6 (3)  Neuromuscular blockade during ICU admission (n, %) 18 (100)  Prone position during ICU admission (n, %) 17 (94) Renal failure  AKI (n, %) 3/18 (16)   AKI I (n, %) 2/3 (66)   AKI III (n, %) 1/3 (33)  CRRT (n, %) 1/18 (6) COVID-19-related therapies  Antivirals (n, %) 14 (77)  Hydroxychloroquine (n, %) 17 (94)  Tocilizumab (n, %) 13 (72)  Methylprednisolone (n, %) 10 (55)  LMWH anticoagulant (n, %) 8 (44) Outcomes  Length of ICU stay (mean, standard deviation, days) 28.4 ± 3.4  Number of hospital survivors (n, %) 18 (100) To our knowledge, this is the first study to analyze the levels of vitamin C in patients with SARS-CoV-2-associated ARDS. Our study revealed that vitamin C levels are undetectable in more than 90% of the patients included. The mechanisms of this significant reduction in vitamin C are uncertain. We hypothesized that several mechanisms, such as increased metabolic consumption due to the enhanced inflammatory response, glomerular hyperfiltration, dialysis, decreased gastrointestinal absorption, or decreased recycling of dehydroascorbate to ascorbic acid, may be involved. Moreover, vitamin C may have implications for treatment of COVID-19-associated ARDS [3]. Indeed, one preclinical study showed that vitamin C increased resistance to infection caused by coronavirus [4]. Moreover, other clinical studies that included surgical patients and patients with pneumonia showed encouraging results in terms of decreased incidence and severity of lung injury and mortality [5]. Our study has several limitations mainly related with the fact that it is a unicentric study with small sample size and blood sample was obtained in different days of their course in the ICU. In conclusion, in our cohort of patients with COVID-19-associated ARDS, the levels of vitamin C are extremely low. Despite the limited generalization of these results, we think these findings might stimulate clinicians to measure vitamin C levels in COVID-19 patients to describe the real impact of this alteration.

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          A new clinical trial to test high-dose vitamin C in patients with COVID-19

          With the 2019 novel coronavirus (2019-nCoV) outbreak now spreading across the world, people are seeking ways in which to potentially protect themselves from the virus or to alleviate its effects once caught. One such means that is being touted online and in the media is vitamin C. Vitamin C is best known for its antioxidant properties, being able to scavenge damaging reactive oxygen species, thus protecting the body’s cells and tissues from oxidative damage and dysfunction. However, the vitamin also has numerous other important functions within the body, many of which are known to support healthy immune function. During infection, vitamin C levels can become depleted and a person’s requirement for vitamin C increases with the severity of the infection [1]. In severe cases, this may require intravenous administration of gram doses in order to achieve high enough levels in the body to compensate for the enhanced turnover of the vitamin. As of February 2020, the clinical characteristics of patients hospitalized with COVID-19-related pneumonia indicated that 26% were transferred to the ICU because of complications such as ARDS and shock [2]. A recently published RCT carried out in the USA in 167 patients with sepsis-related ARDS indicated that administration of ~ 15 g/day of IV vitamin C for 4 days may decrease mortality in these patients [3]. An earlier IV vitamin C trial of patients admitted to the ICU with pneumonia included hydrocortisone administration [4], however, systemic corticosteroid treatment has not been shown to have significant benefits in patients with COVID-19 [5]. Just recently registered on clincialtrials.gov (Identifier: NCT04264533), a new clinical trial to investigate vitamin C infusion for the treatment of severe 2019-nCoV infected pneumonia has begun in Wuhan, China. This is one of the first RCTs to test the effects of IV vitamin C in patients infected with this virus. In this trial, the investigators will treat 140 patients with a placebo control or intravenous vitamin C at a dose of 24 g/day for 7 days. They will assess requirements for mechanical ventilation and vasopressor drugs, organ failure scores, ICU length of stay and 28-day mortality. The investigators of the new study hope to complete the trial by the end of September. Although the findings of this trial will be too late for the many thousands of people currently infected with the virus, the study will nevertheless provide valuable information as to the potential mitigation of symptoms by vitamin C during future viral outbreaks.
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            Author and article information

            Contributors
            jcruiz@vhebron.net
            Journal
            Crit Care
            Critical Care
            BioMed Central (London )
            1364-8535
            1466-609X
            26 August 2020
            26 August 2020
            2020
            : 24
            : 522
            Affiliations
            [1 ]GRID grid.411083.f, ISNI 0000 0001 0675 8654, Intensive Care Department, , Vall d’Hebron Hospital Universitari, Vall d’Hebron Barcelona Hospital Campus, ; Passeig Vall d’Hebron 119-129, Barcelona, 08035 Spain
            [2 ]GRID grid.411083.f, ISNI 0000 0001 0675 8654, Shock, Organ Dysfunction and Resuscitation Research Group, , Vall d’Hebron Hospital Universitari, Vall d’Hebron Barcelona Hospital Campus, ; Passeig Vall d’Hebron 119-129, Barcelona, 08035 Spain
            [3 ]GRID grid.7080.f, Departament de Medicina, , Universitat Autònoma de Barcelona, ; Bellaterra, 08193 Spain
            [4 ]GRID grid.413448.e, ISNI 0000 0000 9314 1427, Ciber Enfermedades Respiratorias (Ciberes), , Instituto de Salud Carlos III, ; Madrid, Spain
            Article
            3249
            10.1186/s13054-020-03249-y
            7447967
            32847620
            e020afd8-ab3b-4d0a-a1e4-742d69bc97f1
            © The Author(s) 2020

            Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

            History
            : 16 July 2020
            : 12 August 2020
            Categories
            Research Letter
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            © The Author(s) 2020

            Emergency medicine & Trauma
            Emergency medicine & Trauma

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