Evidence map›Paper›PMID 40232405›Full record

ArticleAnnals of hematology2025

Assessment of ferritin and hepcidin levels in splenectomised and non-splenectomised β-thalassemia major patients and exploring a potential correlation with von Willebrand factor and ADAMTS-13.

Anwar Al-Awadhi, Materah Salem Alwehaidah, Kefayah Al-Sabaan, Nouf Al-Ajmi

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Article in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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4 authors.

Anwar Al-AwadhiDepartment of Medical Laboratory Sciences, Faculty of Allied Health Sciences, Health Sciences Center, Kuwait University, Jabriya, Kuwait. anwar.alawadhi@ku.edu.kw.ORCID http://orcid.org/0009-0000-1988-0093
Materah Salem AlwehaidahDepartment of Medical Laboratory Sciences, Faculty of Allied Health Sciences, Health Sciences Center, Kuwait University, Jabriya, Kuwait.
Kefayah Al-SabaanDepartment of Hematology, Al-Farwaniya Hospital, Ministry of Health, Farwaniya, Kuwait.
Nouf Al-AjmiDepartment of Medical Laboratory Sciences, Faculty of Allied Health Sciences, Health Sciences Center, Kuwait University, Jabriya, Kuwait.

Funding

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6 · The paper itself

Abstract

Iron overload is a major complication in β-thalassemia major (β-TM) patients, resulting from ineffective erythropoiesis, increased gastrointestinal iron absorption and multiple blood transfusions. Excess iron accumulates in various organs, leading to organ dysfunction, and increased risk of thrombotic events. In this study we aim to determine levels of ferritin and its regulation hormone hepcidin in multi-transfused splenectomised and non-splenectomised β-thalassemia major patients and assess a possible correlation with the coagulation protein von Willebrand factor (vWF) and its cleaving protease ADAMTS-13. The study was conducted on 80 β-thalassemia major patients and 80 age- and sex-matched healthy controls. Plasma levels of vWF, ADAMTS-13, and hepcidin were assessed using the ELISA method. All patients presented with significantly higher levels of ferritin compared to normal controls (p < 0.001), while hepcidin levels were barely higher in patients (p = 0.05). Ferritin had a positive correlation with vWF antigen levels (r = 0.222, p = 0.05), ADAMTS-13 antigen levels (r = 0.334, p = 0.002) and ADAMTS-13 activity levels (r = 0.353, p = 0.001) in patients. Splenectomised patients had significantly higher levels of white blood cell counts, platelet counts and vWF antigen levels compared to non-splenectomised patients (p < 0.05), but ferritin and hepcidin levels were comparable between the two groups (p > 0.05). Hepcidin was not found to be correlated with any of the measured parameters in patients (p > 0.05). Iron overload is well manifested in our study group despite continuous chelation therapy. Unlike hepcidin, ferritin appeared to be associated with increased secretion of vWF and ADAMTS-13 in patients, while splenectomy had no effect on ferritin or hepcidin levels. These findings highlight the importance of proper iron monitoring in β-TM and recognition of thrombotic risks in managing this anemia.

Indexed as

ADAMTS13 Proteinbeta-ThalassemiaFerritinsHepcidinsSplenectomyvon Willebrand FactorAdolescentAdultFemaleHumansIron OverloadMaleYoung AdultADAMTS13 ProteinADAMTS13 protein, humanFerritinsHepcidinsvon Willebrand FactorHepcidinHypercoagulabilityIron overloadSplenectomyThalassemia

Identifiers

PMID40232405
PMCPMC12053081

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