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Evaluation of iron metabolism in hospitalized COVID-19 patients
Thibaud Lefebvre1, Anne Boutten2, Célia Raulet-Bussian2
1Centre Français des Porphyries, Hôpital Louis Mourier, DMU BIOGEM, APHP, Colombes, France; Université Paris Cité, Centre de Recherche sur l'Inflammation, INSERM, UMR1149, Laboratoire d'Excellence GR-Ex, Paris, France.
Insights
COVID-19 significantly alters iron metabolism, with decreased glycosylated ferritin and low iron levels observed. Elevated ferritin and glycosylated ferritin are linked to mortality, suggesting complex iron dysregulation in severe cases.
Area of Science:
- Biochemistry
- Immunology
- Critical Care Medicine
Background:
- Iron metabolism dysregulation is implicated in organ failure in Coronavirus disease 2019 (COVID-19).
- Understanding iron profiles in COVID-19 patients is crucial for managing disease progression and organ damage.
Purpose of the Study:
- To investigate the comprehensive iron metabolism in hospitalized COVID-19 patients.
- To evaluate the influence of tocilizumab on iron parameters and patient outcomes.
Main Methods:
- An observational, multicentric cohort study involving 104 hospitalized COVID-19 patients (66 ICU, 38 medical ward).
- Serum levels of interleukin-6 (IL-6), ferritin, glycosylated ferritin (GF), transferrin, iron, and hepcidin were measured.
- The primary endpoint was mortality.
Main Results:
- Patients exhibited decreased median glycosylated ferritin (35%), low iron concentration (7.5 μmol/L), and low transferrin saturation (21%).
- Hepcidin concentration was elevated (58.7 ng/mL), with some patients showing a dissociation between IL-6 and hepcidin.
- Increased IL-6, ferritin, and GF were independently associated with a higher risk of death, effects amplified by tocilizumab.
Conclusions:
- COVID-19 profoundly alters iron metabolism, deviating from typical inflammatory patterns.
- Uncoupled IL-6/hepcidin levels were observed in a subset of patients.
- The efficacy of additional iron chelation therapy in COVID-19 warrants careful consideration due to these unique metabolic alterations.
Background:
Iron metabolism dysregulation may play a role in organ failure observed in Coronavirus disease 2019 (COVID-19). This study aimed to explore the whole iron metabolism in hospitalized COVID-19 patients and evaluate the impact of tocilizumab.
Methods:
We performed an observational multicentric cohort study, including patients with PCR-provenCOVID-19 from the intensive care unit (ICU) (n = 66) and medical ward (n = 38). We measured serum interleukin-6 (IL-6), ferritin, glycosylated ferritin (GF), transferrin, iron, and hepcidin. The primary outcome was death.
Results:
Among the 104 patients, we observed decreased median GF percentage (35 %; IQ 23-51.5), low iron concentration (7.5 μmol/L; IQ 4-14), normal but low transferrin saturation (TSAT; 21%; IQ 11-33) and increased median hepcidin concentration (58.7 ng/mL; IQ 20.1-92.1). IL-6, ferritin, and GF were independently and significantly associated with death (p = 0.026, p = 0.023, and p = 0.009, respectively). Surprisingly, we observed a decorrelation between hepcidin and IL-6 concentrations in some patients. These findings were amplified in tocilizumab-treated patients.
Conclusion:
Iron metabolism is profoundly modified in COVID-19. The pattern we observed presents differences with a typical inflammation profile. We observed uncoupled IL-6/hepcidin levels in some patients. The benefit of additive iron chelation therapy should be questionable in this setting.
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