Changes in Circulating Adipokine Levels in COVID-19 Patients

Author:

Wikar Tomasz12,Rubinkiewicz Mateusz1ORCID,Stygar Dominika3ORCID,Chełmecka Elżbieta4ORCID,Popiela Urszula1,Michał Wysocki5ORCID,Tylec Piotr6,Maziarz Barbara7,Kukla Michał89

Affiliation:

1. 2nd Department of General Surgery, Jagiellonian University Medical College, 31-066 Kraków, Poland

2. Department of Medical Education, Jagiellonian University Medical College, 31-066 Krakow, Poland

3. Department of Physiology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 41-808 Zabrze, Poland

4. Department of Medical Statistic, Faculty of Pharmaceutical Sciences in Sosnowiec, Medical University of Silesia, 40-055 Sosnowiec, Poland

5. Department of General Surgery and Surgical Oncology, Ludwik Rydygier Memorial Hospital, 31-826 Kraków, Poland

6. Faculty of Medicine, Jagiellonian University Medical College, 31-066 Kraków, Poland

7. Department of Diagnostics, University Hospital, 30-688 Kraków, Poland

8. Department of Internal Medicine and Geriatrics, Faculty of Medicine, Jagiellonian University Medical College, 31-066 Krakow, Poland

9. Department of Endoscopy, University Hospital in Kraków, 30-688 Krakow, Poland

Abstract

Objective: The COVID-19 pandemic has posed significant global health challenges. Despite extensive research efforts, the inflammatory response triggered by SARS-CoV-2 remains to be further explored and understood. Our study aims to examine the changes in serum concentrations of pro-inflammatory adipokines—visfatin and leptin—in COVID-19 patients in relation to a healthy control group. Patients/Materials/Subjects and Methods: The study consisted of forty COVID-19 patients and twenty-four healthy patients in the control group. Two serum samples were collected: upon admission and on the seventh day of hospitalization. Concentrations of visfatin and leptin in the serum, alongside routine biochemical parameters, were measured using enzyme immunoassay or enzyme-linked immunosorbent assay kits. The Shapiro–Wilk test was used to assess normality. Differences between independent groups were compared using the Mann–Whitney U test and Kruskal–Wallis ANOVA. Correlations were evaluated with Spearman’s rank correlation coefficient. Results: Our findings revealed significantly lower visfatin levels in COVID-19 patients compared to the control group upon admission (4.29 ng/mL, (3.0–6.88 ng/mL) vs. 37.16 ng/mL (24.74–50.12 ng/mL), p < 0.001 for visfatin 1 and 52.05 ng/mL, (31.2–69.66 ng/mL) vs. 37.16 ng/mL (24.74–50.12 ng/mL), p = 0.048 for visfatin 2). The visfatin level of COVID-19 patients returned to the normal levels, established in the control group. However, there was no significant difference in leptin levels between the two groups (p = 0.270 for leptin 1 and p = 0.129 for leptin 2). There was a positive correlation between BMI and leptin concentration (r = 0.66 and p = 0.00). Moreover, it was discovered that COVID-19 independently reduces visfatin levels during the first day of illness. Conclusions: The results of our research suggest that the onset of COVID-19 infection is correlated to visfatin levels. Association with leptin levels remains inconclusive. Further research is imperative to elucidate the intricate role of visfatin and leptin in SARS-CoV-2 infection and their potential as biomarkers for COVID-19 severity and prognosis.

Publisher

MDPI AG

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