The Interrelationship between IL-6, 25-OH D, Hepcidin and Anemia in Children with Acute Infectious Disease

הדר מורן-לב 1,2,5 Dror Mandel 3,5 Yosef Weisman 5 Shlomi Cohen 2,5 Amit Ovental 3,5 Marganit Benish 1 Varda Deutsch 4,5 Ronit Lubetzky 1,5
1Pediatrics, Dana Dwek Children's Hospital
2Pediatric Gastroenterology, Dana Dwek Children's Hospital
3Neonatology, Tel Aviv Medical Center
4Hematology Laboratories, Tel Aviv Medical Center
5Sackler Faculty of Medicine, Tel Aviv University

Background: Hepcidin is the master regulator of iron metabolism. Upregulation of hepcidin expression is triggered by proinflamtory cytokines and it considered being a major cause of anemia of inflammation. Recently it has been shown that vitamin D suppresses hepcidin expression.

We aimed to examine the interrelation between hepcidin, vitamin D status and anemia in children with acute infection.

Methods: Ninety one patients (45 girls, 46 boys, mean age 7.3±5) were enrolled after admission to the pediatric ward.
Sixty two patients had infectious disease (30 without anemia and 32 with anemia).
Twenty eight patients were hospitalized for non-infectious causes.
Blood was obtained for measurements of CBC, 25 (OH) D, hepcidin, IL-6, iron and ferritin and compared between 3 groups.

Result: Data is depicted in table 1. Hepcidin and IL-6 were significantly higher in the anemic infectious group compared to non- anemic infectious and control patients. We found vitamin D deficiency in 6 patients with infection and anemia, 2 in the infectious and no anemia group and none in the control group.
Mean 25 (OH) D levels were significantly lower among infectious and anemic patients.
Correlation analyses showed significant associations between hepcidin levels and ferritin (R2 0.47, P-0.001)
and transferrin (R2- 0.57, p<0.001), but not between hepcidin and vitamin D.

Conclusion: We suggest that higher IL-6 and lower 25 (OH)D levels leads to higher hepcidin and

subsequently anemia of acute infection in pediatric population.

*Difference between the anemic infectious paitents to both the infectious with no anemia and control

** difference between anemic infectious to infectious with no anemia

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