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Co-existing iron deficiency/overload in beta-thalassemia trait
Yasar Mehmood Yousafzai1, Qurat Ul Ain Wahid2, Shahtaj Khan3
1Institute of Basic Medical Sciences, Khyber Medical University.
JPMA. the Journal of the Pakistan Medical Association
|June 14, 2019
Summary
Beta thalassaemia trait can present with varying iron levels, including deficiency and overload. This study found that serum ferritin levels in affected individuals can be low, normal, or elevated.
Area of Science:
- Hematology
- Genetics
- Nutritional Science
Background:
- Beta thalassaemia trait is a common inherited blood disorder.
- Iron status assessment in beta thalassaemia trait can be complex due to overlapping clinical presentations.
Purpose of the Study:
- To investigate the co-existence of iron deficiency and iron overload in individuals diagnosed with beta thalassaemia trait.
- To characterize iron status variability within this patient population.
Main Methods:
- A cross-sectional study was conducted with 292 individuals exhibiting a hypochromic microcytic blood picture.
- Haemoglobin electrophoresis and serum ferritin levels were analyzed.
- Data analysis was performed using GraphPad Prism v6.
Main Results:
- Out of 292 subjects, 82.2% were anemic.
- Serum ferritin levels indicated iron deficiency in 18.8% of subjects, iron sufficiency in 70.9%, and iron overload in 10.3%.
- Elevated serum ferritin levels were more prevalent in adults (p<0.001).
Conclusions:
- Serum ferritin levels in individuals with beta thalassaemia trait exhibit significant variability.
- The findings highlight the potential for co-existing iron deficiency and overload, necessitating careful iron status monitoring.
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