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Retrospective analysis of vitamin D status on inflammatory markers and course of the disease in patients with COVID-19 infection.
Ünsal, Y A; Gül, Ö Ö; Cander, S; Ersoy, C; Aydemir, E; Ates, C; Uzun, Z; Armagan, E; Ünsal, O; Ertürk, E.
  • Ünsal YA; Faculty of Medicine, Department of Endocrinology and Diseases of Metabolism, Bursa Uludag University, Bursa, Turkey. yaseminunsalay@gmail.com.
  • Gül ÖÖ; Faculty of Medicine, Department of Endocrinology and Diseases of Metabolism, Bursa Uludag University, Bursa, Turkey.
  • Cander S; Faculty of Medicine, Department of Endocrinology and Diseases of Metabolism, Bursa Uludag University, Bursa, Turkey.
  • Ersoy C; Faculty of Medicine, Department of Endocrinology and Diseases of Metabolism, Bursa Uludag University, Bursa, Turkey.
  • Aydemir E; Faculty of Medicine, Department of Endocrinology and Diseases of Metabolism, Bursa Uludag University, Bursa, Turkey.
  • Ates C; Faculty of Medicine, Department of Endocrinology and Diseases of Metabolism, Bursa Uludag University, Bursa, Turkey.
  • Uzun Z; Faculty of Medicine, Emergency Department, Bursa Uludag University, Bursa, Turkey.
  • Armagan E; Faculty of Medicine, Emergency Department, Bursa Uludag University, Bursa, Turkey.
  • Ünsal O; Faculty of Medicine, Oncology Department, Ankara Gazi University, Ankara, Turkey.
  • Ertürk E; Faculty of Medicine, Department of Endocrinology and Diseases of Metabolism, Bursa Uludag University, Bursa, Turkey.
J Endocrinol Invest ; 44(12): 2601-2607, 2021 Dec.
Article in English | MEDLINE | ID: covidwho-1169067
ABSTRACT

PURPOSE:

The aim of the study was to investigate the association between serum 25-hydroxyvitamin D status within the last 6 months prior to COVID-19 infection and parameters of immune function and clinical outcomes.

METHODS:

Fifty-six patients, who were admitted to the emergency clinic and diagnosed with COVID-19 infection, were included in the study. Data on clinical characteristics, inflammatory parameters and vitamin D status were recorded for each patient. All the participants had data on 25-hydroxyvitamin D status within the last 6 months prior to COVID-19 infection.

RESULTS:

The patients were stratified as those with vitamin D status less than 20 ng/mL and higher than 20 ng/mL. A group with vitamin D status less than 20 ng/mL had lower lymphocyte counts and lower haemoglobin levels that was statistically significant (respectively; p = 0.021, p = 0.035). Higher C-reactive protein (CRP) levels were seen in the vitamin D-deficient group (p = 0.013). It was observed that vitamin D status of the patients who required oxygen therapy were lower than those who did not require oxygen therapy, not statistically significant (p = 0.05). Patients who did not use vitamin D supplementation within 6 months prior to COVID-19 infection had more likely to be diagnosed with pneumonia (p = 0.004).

CONCLUSION:

Cases with lower vitamin D status had increased inflammatory markers and worse clinical outcomes than patients with higher vitamin D status. This study suggests that vitamin D status can be used as a prognostic factor in COVID-19 patients, and vitamin D supplementation can be recommended to improve the clinical outcomes in COVID-19 infection.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Vitamin D / Vitamin D Deficiency / Nutritional Status / COVID-19 Type of study: Observational study / Prognostic study Topics: Long Covid / Traditional medicine Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: English Journal: J Endocrinol Invest Year: 2021 Document Type: Article Affiliation country: S40618-021-01566-9

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Vitamin D / Vitamin D Deficiency / Nutritional Status / COVID-19 Type of study: Observational study / Prognostic study Topics: Long Covid / Traditional medicine Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: English Journal: J Endocrinol Invest Year: 2021 Document Type: Article Affiliation country: S40618-021-01566-9