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Published on: February 19, 2019
Hepcidin levels in children with chronic liver disease
Murat Cakir1, Erol Erduran, Elif Sag Turkmen
1Department of Pediatric Gastroenterology Hepatology and Nutrition, Karadeniz Technical University, Trabzon, Turkey.
Insights
Serum hepcidin levels in children with chronic liver disease (CLD) reflect liver function and antioxidant status. Severe liver fibrosis is linked to a lower hepcidin-to-ferritin ratio in pediatric CLD patients.
Area of Science:
- Pediatric Hepatology
- Biochemistry
- Clinical Research
Background:
- Chronic liver disease (CLD) in children presents complex challenges in assessing disease severity and progression.
- Hepcidin, a key regulator of iron metabolism, and its role in pediatric CLD require further elucidation.
- Understanding the interplay between hepcidin, liver function, and fibrosis is crucial for effective management.
Purpose of the Study:
- To investigate serum hepcidin levels in children diagnosed with chronic liver disease (CLD).
- To analyze the relationship between serum hepcidin and various clinical markers, including cytokines, liver function tests, hepatic iron content, and liver fibrosis.
- To explore the diagnostic and prognostic significance of hepcidin in pediatric CLD.
Main Methods:
- A cohort of 34 children with CLD and 15 healthy controls were enrolled.
- Serum levels of hepcidin, ferritin, iron, IL-6, TGF-β, TOS, and TAS were measured.
- Liver iron content (LIC) was assessed via liver biopsy, alongside evaluation of liver fibrosis staging.
Main Results:
- Children with CLD exhibited significantly higher serum ferritin levels compared to controls.
- No significant difference in overall hepcidin levels was observed between CLD patients and controls.
- Hepcidin positively correlated with ferritin, PELD score, and TAS, but negatively with albumin.
- Severe fibrosis was associated with lower transferrin saturation and a reduced hepcidin:ferritin ratio.
Conclusions:
- Serum hepcidin levels in pediatric CLD patients are indicative of liver function and antioxidant status.
- A low hepcidin-to-ferritin ratio is a significant indicator of severe liver fibrosis in children with CLD.
- These findings highlight the potential utility of hepcidin and related markers in managing pediatric liver disease.
Background/Aim:
We aimed to analyze serum hepcidin level in children with chronic liver disease (CLD) and its relationship with serum cytokines level, liver function tests, hepatic iron content, and liver fibrosis.
Patients And Methods:
The study included 34 children with CLD, and 15 age- and gender-matched healthy children. Serum hepcidin, ferritin, iron level, interleukin-6 (IL-6), transforming growth factor-β (TGF-β ), total oxidant status (TOS), and antioxidant status (TAS) were studied in all patients and in the control group. Liver iron content (LIC) was measured from the liver biopsy specimen.
Results:
Serum ferritin levels were higher in patients with CLD than control group (100.1 ± 98.2 ng/mL vs 50.5 ± 32.2 ng/mL, P = 0.016). No significant difference was found in hepcidin levels. Hepcidin levels in children with CLD was positively correlated with ferritin (r = 0.75, P = 0.001), pediatric end-stage liver disease (PELD) score (r = 0.56, P = 0.001), TAS (r = 0.42,P = 0.02), but negatively correlated with albumin level (r = -0.45,P = 0.008). Transferrin saturation and hepcidin:ferritin ratio were significantly low in patients with severe fibrosis compared with patients with mild/without fibrosis (15.5 ± 5.5 vs 34.3 ± 30.1, P = 0.017 and 1 ± 0.5 vs 1.9 ± 1.4,P = 0.04, respectively).
Conclusion:
Serum hepcidin levels in children with CLD reflect both liver functions and TAS, and severe fibrosis is associated with low hepcidin:ferritin ratio in children with CLD.
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