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Urinary hepcidin level as an early predictor of iron deficiency in children: A case control study
Mohammed Sanad1, Amal F Gharib
1Department of Pediatrics, Faculty of Medicine, Zagazig University, Egypt. zanad_zanad2005@yahoo.com
Insights
Urinary hepcidin-25 levels can predict iron deficiency in children before anemia develops. This non-invasive test shows lower levels with increasing iron deficiency severity.
Area of Science:
- Pediatric Hematology
- Biochemistry
- Diagnostic Medicine
Background:
- Early detection of iron deficiency (ID) is crucial, ideally before anemia manifests.
- Current screening methods may not identify iron deficiency in its earliest stages.
- Hepcidin, a key iron-regulating hormone, is a potential biomarker for iron status.
Purpose of the Study:
- To evaluate the role of urinary hepcidin-25 levels in the early prediction of iron deficiency in children.
- To assess the correlation between urinary hepcidin-25 and established iron status parameters.
- To determine the diagnostic accuracy of urinary hepcidin-25 for different stages of iron deficiency.
Main Methods:
- A case-control study involving 100 children (25 each of ID stage-1, ID stage-2, ID stage-3, and healthy controls).
- Measurement of iron status parameters including hemoglobin, ferritin, and transferrin.
- Quantification of urinary hepcidin-25 levels and correlation with clinical parameters.
Main Results:
- Urinary hepcidin-25 levels were significantly lower in all stages of iron deficiency compared to controls.
- A progressive decrease in urinary hepcidin-25 was observed with increasing severity of iron deficiency.
- Urinary hepcidin-25 demonstrated high sensitivity and specificity in predicting all stages of iron deficiency, with specific cutoff values established for each stage.
Conclusions:
- Urinary hepcidin-25 is a simple, non-invasive biomarker for early iron deficiency detection in children.
- This marker can predict iron deficiency before the onset of hematological changes like anemia.
- Urinary hepcidin-25 offers a promising tool for early diagnosis and management of pediatric iron deficiency.
Background:
The ideal screening test would be capable of identifying iron deficiency in the absence of anemia. We tried to detect role of urinary hepcidin-25 level in early prediction of iron deficiency in children.
Methods:
This is a case control study performed on 100 children in Hematology Unit of Pediatric Department, Zagazig University Hospital, Egypt. Our study included 25 cases of iron deficiency (ID) stage-1 (iron depletion), 25 cases ID stage-2 (iron-deficient erythropoiesis), 25 cases ID stage-3 (iron deficiency anemia) and 25 healthy children as a control group. Estimation of iron status parameters was done. Urinary hepcidin-25 level was detected.
Results:
Urinary hepcidin-25 level was significantly lower in all stages of iron deficiency than in control group, more significant reduction in its level was observed with the progress in severity of iron deficiency. Urinary hepcidin showed significant positive correlation with hemoglobin, mean corpuscular volume, hematocrit value, serum iron and ferritin and transferrin saturation. In contrary, it showed significant negative correlation with serum transferrin and total iron binding capacity.Urinary hepcidin at cutoff point ≤0.94 nmol/mmol Cr could Predict ID stage-1 with sensitivity 88% and specificity 88%. Cutoff point ≤0.42 nmol/mmol Cr could predict ID stage-2 with sensitivity 96% and specificity 92%. Cutoff point ≤0.08 nmol/mmol Cr could Predict ID stage-3 with Sensitivity 96% and specificity 100%.
Conclusions:
We can conclude that detection of urinary hepcidin-25 level was a simple and non invasive test and could predict iron deficiency very early, before appearance of hematological affections.
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