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Erythroferrone in β-thalassemia: Systematic review and meta-analysis
Muhammad Saboor1, Khaled Abass2
1Department of Medical Laboratory Sciences, College of Health Sciences, University of Sharjah, Sharjah, United Arab Emirates; Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah, United Arab Emirates.
Erythroferrone (ERFE) is significantly elevated in beta-thalassemia, showing a strong inverse correlation with hepcidin. This meta-analysis confirms ERFE
Area of Science:
- Hematology
- Biomarker Discovery
- Molecular Biology
Background:
- Beta-thalassemia is a genetic blood disorder characterized by ineffective erythropoiesis.
- Erythroferrone (ERFE) is a hormone that suppresses hepcidin, playing a role in iron regulation.
- ERFE is a potential biomarker for ineffective erythropoiesis, but quantitative data synthesis is lacking.
Conclusions:
- Circulating ERFE levels are markedly elevated in beta-thalassemia and inversely correlate with hepcidin in a reproducible manner.
- ERFE shows potential as a biomarker for ineffective erythropoiesis in beta-thalassemia.
- Assay standardization and prospective validation are necessary for clinical application.
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