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Hepcidin and iron parameters in children with anemia of chronic disease and iron deficiency anemia
Gunjan Mahajan1, Sunita Sharma1, Jagdish Chandra2
1Department of Pathology, Lady Hardinge Medical College, New Delhi, India.
Insights
Hepcidin aids in distinguishing anemia of chronic disease (ACD) from iron deficiency anemia (IDA). This biomarker also helps identify iron deficiency in ACD patients, guiding appropriate therapy selection.
Area of Science:
- Pediatric Hematology
- Clinical Biochemistry
- Iron Metabolism
Background:
- Anemia of chronic disease (ACD) and iron deficiency anemia (IDA) are common, often overlapping anemias.
- Hepcidin, a key regulator of iron metabolism, is a novel biomarker for iron status assessment.
- Differentiating ACD from IDA and identifying coexistent iron deficiency in ACD is clinically significant.
Purpose of the Study:
- To investigate the role of serum hepcidin and conventional iron parameters in differentiating ACD from IDA in children.
- To identify children with ACD who also have iron deficiency (ID).
- To assess the utility of hepcidin in guiding therapeutic decisions for pediatric anemia.
Main Methods:
- A comparative study involving 30 pediatric cases each of ACD and IDA, plus 30 age/sex-matched controls.
- ACD cases were subcategorized into pure ACD and ACD with coexistent ID.
- Analysis included complete blood count, inflammatory markers (CRP, IL-6), iron studies, soluble transferrin receptor (sTfR), and serum hepcidin.
Main Results:
- Serum hepcidin levels were significantly elevated in pure ACD patients (143.85±42.76 ng/mL) compared to IDA patients (6.01±2.83 ng/mL) and controls (24.96±9.09 ng/mL).
- ACD patients with coexistent ID exhibited significantly lower serum hepcidin (10.0±2.97 ng/mL) compared to pure ACD patients.
- Elevated sTfR levels in ACD patients correlated with reduced hepcidin, indicating coexistent iron deficiency.
Conclusions:
- Serum hepcidin is a valuable biomarker for differentiating pediatric ACD from IDA.
- Hepcidin measurement effectively identifies iron deficiency in children with ACD.
- These findings support the use of hepcidin assays to guide targeted anemia therapy.
Background:
Anemia of chronic disease (ACD) and iron deficiency anemia (IDA) are the two most prevalent forms of anemia having interrelated characteristics. Hepcidin, a newly introduced biomarker for assessment of iron status, is a homeostatic regulator of iron metabolism. We investigated the role of hepcidin and other conventional iron parameters to assess iron status among children with ACD and IDA. We also identified children with ACD who developed iron deficiency (ID).
Methods:
The study was undertaken in anemic children with 30 cases each of ACD and IDA along with 30 age and sex-matched controls. The ACD cases were subdivided into pure ACD and ACD with coexistent ID. All cases were subjected to following tests: complete blood count with peripheral smear, serum C-reactive protein, serum interleukin-6, iron studies, serum soluble transferrin receptor (sTfR), and serum hepcidin.
Results:
The mean serum hepcidin concentration was significantly increased in pure ACD patients (143.85±42.76 ng/mL) as compared to those in IDA patients (6.01±2.83 ng/mL, P < 0.001) and controls (24.96±9.09 ng/mL, P <0.001). Also, compared to pure ACD patients [normal sTfR levels (<3 µg/mL)], the serum hepcidin concentration was reduced significantly in ACD patients with ID [high sTfR levels (≥3 µg/mL)] with a mean of 10.0±2.97 ng/mL.
Conclusion:
Hepcidin measurement can provide a useful tool for differentiating ACD from IDA and also help to identify an iron deficiency in ACD patients. This might aid in the appropriate selection of therapy for these patients.
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