Vitamin D Deficiency and Outcome of COVID-19 Patients
Infection with the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) poses an enormous challenge to health care systems throughout the world. Without causal treatment, identification of modifiable prognostic factors may help to improve outcomes. To explore possible associations of vitamin...
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| Published in | Nutrients Vol. 12; no. 9; p. 2757 |
|---|---|
| Main Authors | , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Switzerland
MDPI AG
10.09.2020
MDPI |
| Subjects | |
| Online Access | Get full text |
| ISSN | 2072-6643 2072-6643 |
| DOI | 10.3390/nu12092757 |
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| Abstract | Infection with the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) poses an enormous challenge to health care systems throughout the world. Without causal treatment, identification of modifiable prognostic factors may help to improve outcomes. To explore possible associations of vitamin D (VitD) status with disease severity and survival, we studied 185 patients diagnosed with coronavirus disease 2019 (COVID-19) and treated at our center. VitD status at first presentation was assessed retrospectively using accredited laboratory methods. VitD deficiency was defined as serum total 25-hydroxyvitamin D level < 12 ng/mL (<30 nM). Primary endpoint was severe course of disease (i.e., need for invasive mechanical ventilation and/or death, IMV/D). Within a median observation period of 66 days (range 2–92), 23 patients required IMV. A total of 28 patients had IMV/D, including 16 deaths. Ninety-three (50%) patients required hospitalization (inpatient subgroup). A total of 41 (22%) patients were VitD deficient. When adjusted for age, gender, and comorbidities, VitD deficiency was associated with higher risk of IMV/D and death (HR 6.12, 95% CI 2.79–13.42, p < 0.001 and HR 14.73, 95% CI 4.16–52.19, p < 0.001, respectively). Similar correlations were observed in the inpatient subgroup. Our study demonstrates an association between VitD deficiency and severity/mortality of COVID-19, highlighting the need for interventional studies on VitD supplementation in SARS-CoV-2 infected individuals. |
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| AbstractList | Infection with the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) poses an enormous challenge to health care systems throughout the world. Without causal treatment, identification of modifiable prognostic factors may help to improve outcomes. To explore possible associations of vitamin D (VitD) status with disease severity and survival, we studied 185 patients diagnosed with coronavirus disease 2019 (COVID-19) and treated at our center. VitD status at first presentation was assessed retrospectively using accredited laboratory methods. VitD deficiency was defined as serum total 25-hydroxyvitamin D level < 12 ng/mL (<30 nM). Primary endpoint was severe course of disease (i.e., need for invasive mechanical ventilation and/or death, IMV/D). Within a median observation period of 66 days (range 2–92), 23 patients required IMV. A total of 28 patients had IMV/D, including 16 deaths. Ninety-three (50%) patients required hospitalization (inpatient subgroup). A total of 41 (22%) patients were VitD deficient. When adjusted for age, gender, and comorbidities, VitD deficiency was associated with higher risk of IMV/D and death (HR 6.12, 95% CI 2.79–13.42, p < 0.001 and HR 14.73, 95% CI 4.16–52.19, p < 0.001, respectively). Similar correlations were observed in the inpatient subgroup. Our study demonstrates an association between VitD deficiency and severity/mortality of COVID-19, highlighting the need for interventional studies on VitD supplementation in SARS-CoV-2 infected individuals. Infection with the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) poses an enormous challenge to health care systems throughout the world. Without causal treatment, identification of modifiable prognostic factors may help to improve outcomes. To explore possible associations of vitamin D (VitD) status with disease severity and survival, we studied 185 patients diagnosed with coronavirus disease 2019 (COVID-19) and treated at our center. VitD status at first presentation was assessed retrospectively using accredited laboratory methods. VitD deficiency was defined as serum total 25-hydroxyvitamin D level < 12 ng/mL (<30 nM). Primary endpoint was severe course of disease (i.e., need for invasive mechanical ventilation and/or death, IMV/D). Within a median observation period of 66 days (range 2-92), 23 patients required IMV. A total of 28 patients had IMV/D, including 16 deaths. Ninety-three (50%) patients required hospitalization (inpatient subgroup). A total of 41 (22%) patients were VitD deficient. When adjusted for age, gender, and comorbidities, VitD deficiency was associated with higher risk of IMV/D and death (HR 6.12, 95% CI 2.79-13.42, p < 0.001 and HR 14.73, 95% CI 4.16-52.19, p < 0.001, respectively). Similar correlations were observed in the inpatient subgroup. Our study demonstrates an association between VitD deficiency and severity/mortality of COVID-19, highlighting the need for interventional studies on VitD supplementation in SARS-CoV-2 infected individuals.Infection with the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) poses an enormous challenge to health care systems throughout the world. Without causal treatment, identification of modifiable prognostic factors may help to improve outcomes. To explore possible associations of vitamin D (VitD) status with disease severity and survival, we studied 185 patients diagnosed with coronavirus disease 2019 (COVID-19) and treated at our center. VitD status at first presentation was assessed retrospectively using accredited laboratory methods. VitD deficiency was defined as serum total 25-hydroxyvitamin D level < 12 ng/mL (<30 nM). Primary endpoint was severe course of disease (i.e., need for invasive mechanical ventilation and/or death, IMV/D). Within a median observation period of 66 days (range 2-92), 23 patients required IMV. A total of 28 patients had IMV/D, including 16 deaths. Ninety-three (50%) patients required hospitalization (inpatient subgroup). A total of 41 (22%) patients were VitD deficient. When adjusted for age, gender, and comorbidities, VitD deficiency was associated with higher risk of IMV/D and death (HR 6.12, 95% CI 2.79-13.42, p < 0.001 and HR 14.73, 95% CI 4.16-52.19, p < 0.001, respectively). Similar correlations were observed in the inpatient subgroup. Our study demonstrates an association between VitD deficiency and severity/mortality of COVID-19, highlighting the need for interventional studies on VitD supplementation in SARS-CoV-2 infected individuals. Infection with the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) poses an enormous challenge to health care systems throughout the world. Without causal treatment, identification of modifiable prognostic factors may help to improve outcomes. To explore possible associations of vitamin D (VitD) status with disease severity and survival, we studied 185 patients diagnosed with coronavirus disease 2019 (COVID-19) and treated at our center. VitD status at first presentation was assessed retrospectively using accredited laboratory methods. VitD deficiency was defined as serum total 25-hydroxyvitamin D level < 12 ng/mL (<30 nM). Primary endpoint was severe course of disease (i.e., need for invasive mechanical ventilation and/or death, IMV/D). Within a median observation period of 66 days (range 2-92), 23 patients required IMV. A total of 28 patients had IMV/D, including 16 deaths. Ninety-three (50%) patients required hospitalization (inpatient subgroup). A total of 41 (22%) patients were VitD deficient. When adjusted for age, gender, and comorbidities, VitD deficiency was associated with higher risk of IMV/D and death (HR 6.12, 95% CI 2.79-13.42, < 0.001 and HR 14.73, 95% CI 4.16-52.19, < 0.001, respectively). Similar correlations were observed in the inpatient subgroup. Our study demonstrates an association between VitD deficiency and severity/mortality of COVID-19, highlighting the need for interventional studies on VitD supplementation in SARS-CoV-2 infected individuals. |
| Author | Boxberger, Monica Merle, Uta Dreher, Saida Tiwari-Heckler, Shilpa Radujkovic, Aleksandar Hippchen, Theresa |
| AuthorAffiliation | 2 Department of Internal Medicine IV, University of Heidelberg, 69121 Heidelberg, Germany; theresa.hippchen@med.uni-heidelberg.de (T.H.); shilpa.tiwari-heckler@med.uni-heidelberg.de (S.T.-H.); saida.dreher@med.uni-heidelberg.de (S.D.); monica.boxberger@med.uni-heidelberg.de (M.B.) 1 Department of Internal Medicine V, University of Heidelberg, 69121 Heidelberg, Germany; aleksandar.radujkovic@med.uni-heidelberg.de |
| AuthorAffiliation_xml | – name: 1 Department of Internal Medicine V, University of Heidelberg, 69121 Heidelberg, Germany; aleksandar.radujkovic@med.uni-heidelberg.de – name: 2 Department of Internal Medicine IV, University of Heidelberg, 69121 Heidelberg, Germany; theresa.hippchen@med.uni-heidelberg.de (T.H.); shilpa.tiwari-heckler@med.uni-heidelberg.de (S.T.-H.); saida.dreher@med.uni-heidelberg.de (S.D.); monica.boxberger@med.uni-heidelberg.de (M.B.) |
| Author_xml | – sequence: 1 givenname: Aleksandar surname: Radujkovic fullname: Radujkovic, Aleksandar – sequence: 2 givenname: Theresa surname: Hippchen fullname: Hippchen, Theresa – sequence: 3 givenname: Shilpa surname: Tiwari-Heckler fullname: Tiwari-Heckler, Shilpa – sequence: 4 givenname: Saida surname: Dreher fullname: Dreher, Saida – sequence: 5 givenname: Monica surname: Boxberger fullname: Boxberger, Monica – sequence: 6 givenname: Uta orcidid: 0000-0003-1386-3350 surname: Merle fullname: Merle, Uta |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32927735$$D View this record in MEDLINE/PubMed |
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| ContentType | Journal Article |
| Copyright | 2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2020 by the authors. 2020 |
| Copyright_xml | – notice: 2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: 2020 by the authors. 2020 |
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| DOI | 10.3390/nu12092757 |
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| References | Chen (ref_2) 2020; 395 Shi (ref_4) 2020; 24 ref_14 Faul (ref_23) 2020; 113 ref_24 Mitchell (ref_9) 2020; 8 ref_12 Jakovac (ref_13) 2020; 318 Verity (ref_16) 2020; 20 ref_11 ref_22 Yang (ref_3) 2020; 94 ref_21 Dong (ref_1) 2020; 20 Martineau (ref_20) 2020; 8 Martineau (ref_7) 2017; 356 ref_19 ref_17 Marik (ref_8) 2020; 6 ref_15 Rhodes (ref_10) 2020; 51 Schemper (ref_18) 1996; 17 ref_5 Holick (ref_6) 2007; 357 |
| References_xml | – ident: ref_12 doi: 10.1007/s40520-020-01650-9 – volume: 356 start-page: i6583 year: 2017 ident: ref_7 article-title: Vitamin D supplementation to prevent acute respiratory tract infections: Systematic review and meta-analysis of individual participant data publication-title: BMJ doi: 10.1136/bmj.i6583 – volume: 20 start-page: 669 year: 2020 ident: ref_16 article-title: Estimates of the severity of coronavirus disease 2019: A model-based analysis publication-title: Lancet Infect. Dis. doi: 10.1016/S1473-3099(20)30243-7 – ident: ref_22 doi: 10.1002/jmv.26360 – ident: ref_24 doi: 10.1186/s12889-015-2016-7 – volume: 357 start-page: 266 year: 2007 ident: ref_6 article-title: Vitamin D Deficiency publication-title: N. Engl. J. Med. doi: 10.1056/NEJMra070553 – ident: ref_21 doi: 10.3390/nu12051359 – volume: 318 start-page: E589 year: 2020 ident: ref_13 article-title: COVID-19 and vitamin D—Is there a link and an opportunity for intervention? publication-title: Am. J. Physiol. Metab. – volume: 17 start-page: 343 year: 1996 ident: ref_18 article-title: A note on quantifying follow-up in studies of failure time publication-title: Control. Clin. Trials doi: 10.1016/0197-2456(96)00075-X – volume: 24 start-page: 1 year: 2020 ident: ref_4 article-title: Host susceptibility to severe COVID-19 and establishment of a host risk score: Findings of 487 cases outside Wuhan publication-title: Crit. Care doi: 10.1186/s13054-020-2833-7 – volume: 51 start-page: 1434 year: 2020 ident: ref_10 article-title: Editorial: Low population mortality from COVID-19 in countries south of latitude 35 degrees North supports vitamin D as a factor determining severity publication-title: Aliment. Pharmacol. Ther. doi: 10.1111/apt.15777 – volume: 8 start-page: 735 year: 2020 ident: ref_20 article-title: Vitamin D for COVID-19: A case to answer? publication-title: Lancet Diabetes Endocrinol. doi: 10.1016/S2213-8587(20)30268-0 – volume: 113 start-page: 84 year: 2020 ident: ref_23 article-title: Vitamin D Deficiency and ARDS after SARS-CoV-2 Infection publication-title: Ir. Med. J. – volume: 395 start-page: 507 year: 2020 ident: ref_2 article-title: Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: A descriptive study publication-title: Lancet doi: 10.1016/S0140-6736(20)30211-7 – ident: ref_5 doi: 10.3390/nu12072097 – volume: 6 start-page: 100041 year: 2020 ident: ref_8 article-title: Does vitamin D status impact mortality from SARS-CoV-2 infection? publication-title: Med. Drug Discov. doi: 10.1016/j.medidd.2020.100041 – ident: ref_15 – ident: ref_17 doi: 10.1016/j.annemergmed.2020.06.001 – ident: ref_14 doi: 10.3389/fimmu.2020.01523 – ident: ref_19 – ident: ref_11 doi: 10.20944/preprints202003.0235.v2 – volume: 94 start-page: 91 year: 2020 ident: ref_3 article-title: Prevalence of comorbidities and its effects in patients infected with SARS-CoV-2: A systematic review and meta-analysis publication-title: Int. J. Infect. Dis. doi: 10.1016/j.ijid.2020.03.017 – volume: 8 start-page: 570 year: 2020 ident: ref_9 article-title: Vitamin-D and COVID-19: Do deficient risk a poorer outcome? publication-title: Lancet Diabetes Endocrinol. doi: 10.1016/S2213-8587(20)30183-2 – volume: 20 start-page: 533 year: 2020 ident: ref_1 article-title: An interactive web-based dashboard to track COVID-19 in real time publication-title: Lancet Infect. Dis. doi: 10.1016/S1473-3099(20)30120-1 |
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| Title | Vitamin D Deficiency and Outcome of COVID-19 Patients |
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