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Reference limits and behaviour of serum transferrin receptor in children 6-10 years of age
P Danise1, M Maconi, G Morelli
1Laboratory of Hematology, Umberto I Hospital, Nocera Inferiore (Sa), Italy.
Insights
Serum transferrin receptor (sTfR) is a useful marker for iron deficiency and erythropoiesis in children. While not definitive alone, sTfR aids in diagnosing conditions like Beta-thalassemia trait when used with other tests.
Area of Science:
- Pediatric Hematology
- Clinical Biochemistry
- Erythropoiesis Studies
Background:
- Serum transferrin receptor (sTfR) is primarily produced by erythroblasts and reticulocytes.
- sTfR serves as a clinical marker for accelerated erythropoiesis and iron deficiency.
- Assessing sTfR is valuable during periods of rapid growth in infancy, childhood, and adolescence.
Purpose of the Study:
- To evaluate sTfR and other erythropoiesis/iron storage parameters in children aged 6-10 years.
- To establish reference intervals for sTfR by sex and age in healthy children.
- To compare sTfR and related markers across healthy, iron-deficient, and Beta-thalassemia trait groups.
Main Methods:
- Analyzed sTfR, hemoglobin (Hb), MCV, CHr, Ret-He, serum ferritin, and sTfR/ferritin index in 916 children.
- Stratified children into healthy, storage iron deficiency, and Beta-thalassemia trait groups.
- Determined age- and sex-specific reference intervals for sTfR in healthy children.
Main Results:
- sTfR demonstrated a slight, statistically significant age-related increase, with no significant sex differences.
- Compared to healthy children, sTfR and other parameters varied across iron deficiency and Beta-thalassemia trait groups.
- sTfR alone was not decisive for borderline cases but contributed to a comprehensive diagnostic panel.
Conclusions:
- sTfR is a valuable, albeit not standalone, indicator in pediatric hematology.
- The study established reference intervals for sTfR in children aged 6-10 years.
- sTfR aids in the diagnostic workup of iron deficiency and Beta-thalassemia trait in pediatric populations.
Abstract:
Serum transferrin receptor (sTfR) originates mostly from erythroblasts and lesser from reticulocytes. The usefulness of sTfR has been implicated in several clinical situations, mainly as a marker of accelerated erythropoiesis or iron deficiency. The assessment of sTfR may be useful in the period of rapid growth during infancy, childhood and adolescence. We evaluated sTfR and the other quantitative and qualitative parameters of the erythropoiesis (Hb, MCV, CHr, Ret-He) and of the iron storage (serum ferritin, sTfR/ferritin index) in a total of 916 children aged 6-10 years. Children were divided into three groups: (A) healthy children, (B) with storage iron deficiency (serum ferritin < 12 microg/l) and (C) Beta trait carriers (HbA2 > 3.3). We determined reference intervals by sex and by age in healthy children. sTfR showed a slight but statistically significant age related increase but did not show significant sex differences. We compared sTfR and the other parameters investigated in the three groups of children. sTfR is not a decisive parameter that can be utilized alone in discriminating the border-line situations between normal and pathologic ones but can help in completing the panel of tests in iron deficiency and in thalassaemia Beta trait carriers.
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