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Serum omentin and chemerin levels in patients with coronavirus disease 2019
Tomasz Maksymilian Wikar1, Michał Zdzisław Kukla2,3, Dominika Stygar4
12nd Department of General Surgery, Jagiellonian University Medical College, Kraków, Poland.
Insights
In coronavirus disease 2019 (COVID-19), circulating chemerin levels are elevated, suggesting a role in the inflammatory response. Omentin levels, however, remain unchanged in COVID-19 patients compared to controls.
Area of Science:
- Biochemistry
- Immunology
- Infectious Diseases
Background:
- Chemerin and omentin are adipokines with distinct inflammatory roles.
- Their specific involvement in COVID-19 pathogenesis is not fully understood.
- Existing data on adipokine profiles in COVID-19 are inconsistent.
Purpose of the Study:
- To investigate the serum concentrations of chemerin and omentin in hospitalized COVID-19 patients.
- To compare adipokine levels between COVID-19 patients and non-COVID controls.
- To assess changes in chemerin and omentin levels during hospitalization.
Main Methods:
- A single-center case-control study involving 40 COVID-19 patients and 24 controls.
- Serum samples collected on admission (Day 0) and Day 7 for COVID-19 patients.
- Enzyme immunoassays used to measure serum omentin, chemerin, and inflammatory markers.
Main Results:
- COVID-19 patients exhibited higher levels of inflammatory markers (CRP, ferritin, IL-6, D-dimer) than controls.
- Baseline serum omentin concentrations were similar between COVID-19 patients and controls and remained stable.
- Baseline chemerin levels were significantly higher in COVID-19 patients and remained elevated throughout hospitalization.
Conclusions:
- COVID-19 is associated with sustained elevation of circulating chemerin.
- Omentin levels do not appear to be altered in COVID-19 patients.
- Chemerin may play a role in the systemic inflammatory response to SARS-CoV-2 infection.
Background:
Chemerin and omentin are adipokines secreted mainly by visceral adipose tissue, with pro- and anti-inflammatory properties, respectively. Their role in coronavirus disease 2019 (COVID-19) remains incompletely understood and available data are inconsistent.
Methods:
This single-center case-control study included 40 hospitalized patients with COVID-19 and 24 non-COVID controls. Serum samples were collected in COVID-19 patients on admission (Day 0) and on Day 7 of hospitalization, and once in controls. Concentrations of omentin and chemerin and routine laboratory parameters were measured using enzyme immunoassays.
Results:
Compared with controls, patients with COVID-19 had higher inflammatory markers, including C-reactive protein, ferritin, interleukin-6 and D-dimer. Baseline serum omentin concentrations did not differ between COVID-19 patients and controls (363.6 [245.2-513.0] vs. 368.9 [254.1-468.8] ng/mL; p = 0.994), and remained stable between Day 0 and Day 7 (p = 0.605). In contrast, baseline chemerin levels were significantly higher in COVID-19 patients than in controls (234.3 [164.9-269.9] vs. 144.7 [98.0-213.2] ng/mL; p = 0.001) and remained elevated at Day 7 (243.7 [171.0-376.7] ng/mL, p = 0.001 vs. controls), with a non-significant trend toward an increase over time (Δ chemerin +42.6 ng/mL; p = 0.071).
Conclusion:
In this cohort of hospitalized but predominantly non-critically ill patients, COVID-19 was associated with sustained elevation of circulating chemerin but not with alterations in omentin levels. Our findings are consistent with a potential role for chemerin, but not omentin, in the systemic inflammatory response to SARS-CoV-2 infection and complement previous reports describing divergent adipokine profiles in COVID-19.
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