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Published on: January 31, 2022
Low serum lipocalin levels in patients with iron deficiency anemia
Baris Malbora1, Zekai Avci, Meltem Gülsan
1Departments of Pediatric Hematology, Faculty of Medicine, Baskent University, Ankara, Turkey. barismalbora@gmail.com
Insights
Serum lipocalin levels were lower in children with iron deficiency anemia (IDA) before treatment. After iron therapy, lipocalin levels normalized, suggesting iron deficiency, not anemia, impacts lipocalin.
Area of Science:
- Pediatric Hematology
- Biochemistry
Background:
- Lipocalin is a protein with known associations with anemia.
- No prior studies have investigated the relationship between lipocalin and iron deficiency anemia (IDA).
Purpose of the Study:
- To investigate serum lipocalin levels in children with IDA before and after iron therapy.
- To compare lipocalin levels in children with IDA to healthy controls.
Main Methods:
- A study involving 61 children, with 30 diagnosed with IDA and 30 healthy controls.
- IDA patients received oral ferrous sulfate therapy.
- Serum lipocalin levels were measured at admission and after three months of treatment.
Main Results:
- Children with IDA had significantly lower serum lipocalin levels at admission compared to healthy controls (31.01±14.46 vs. 57.35±39.51 ng/dL).
- Following iron therapy, serum lipocalin levels in IDA patients increased significantly (to 74.77 ng/dL), normalizing the difference compared to controls.
- No significant difference in lipocalin levels was observed between groups after treatment.
Conclusions:
- Decreased serum lipocalin levels in children with IDA appear to be a consequence of iron deficiency itself, rather than anemia.
- Lipocalin may serve as a potential biomarker for iron deficiency.
Abstract:
In the recent literature, there are studies on the relationship between anemia and lipocalin, but there is no study regarding the relationship between lipocalin and iron deficiency anemia (IDA) up to date. In this study, we aimed to observe lipocalin levels at admission, and after iron therapy in children with IDA. We also compared our findings to those in healthy children. Sixty-one children admitted in our outpatient clinic were included in the study. Thirty of these children had IDA (study group) and the rest were healthy (control group). Thirty patients, meeting the IDA criteria, received oral ferrous sulfate of 4 mg/kg/d. As soon as the hemoglobin value reached >11 g/dL, half dose of oral ferrous sulfate therapy was continued for another month. Serum lipocalin levels before and after iron therapies were compared. Hematologic parameters and serum lipocalin levels were also compared between the 2 groups. Mean values of serum lipocalin were 31.01±14.46 and 74.77 ng/dL in patients with IDA at admission and at third month of therapy, respectively (P<0.0001). The same figure was 57.35±39.51 ng/dL in the control group. Before treatment, mean values of lipocalin levels in patients with IDA was significantly lower than the control group (P=0.001); however, such a difference was not detected after 3 months of therapy (P=0.102). We suggest that decreased serum lipocalin levels in our patients during iron insufficiency were caused by iron deficiency rather than anemia.
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