Literature DB >> 35958503

Phosphatidylserine-exposed red blood cells and ineffective erythropoiesis biomarkers in patients with thalassemia.

Siriyakorn Chansai1,2, Supawadee Yamsri2, Supan Fucharoen2, Goonnapa Fucharoen2, Nattiya Teawtrakul3.   

Abstract

OBJECTIVE: The degree of ineffective erythropoiesis is known to be associated with clinical severity among individuals with thalassemia. The association of ineffective erythropoiesis biomarker levels with different thalassemia genotypes, however, remains limited. The aim of this study was to explore the level of phosphatidylserine-exposed red blood cells (PS-exposed RBCs) and ineffective erythropoiesis biomarkers (growth-differentiation factor-15 and soluble transferrin receptors) in patients with different genotypes.
METHODS: A cross-sectional study was conducted on 139 patients of age 18 years and above with different genotypes at Srinagarind Hospital, Khon Kaen University, Thailand. The levels of PS-exposed RBCs were determined using flow cytometry. Measurements of growth-differentiation factor-15 (GDF-15) and soluble transferrin receptors (sTfR) were evaluated by the ELISA method.
RESULTS: The PS-exposed RBCs levels were found to be significantly higher in splenectomized beta-thalassemia patients. Patients with beta-thalassemia had the highest GDF-15 levels, followed by patients with non-deletional alpha-thalassemia. Patients with non-deletional alpha-thalassemia showed elevated hemoglobin levels and reduced GDF-15 levels after splenectomy. Patients with beta-thalassemia and non-deletional alpha-thalassemia had the highest levels of PS-exposed RBCs and ineffective erythropoiesis biomarkers, which correlated with the clinical severity of thalassemia.
CONCLUSIONS: The levels of ineffective erythropoiesis biomarkers were different across thalassemia genotypes. Splenectomy may improve clinical symptoms of patients with non-deletional alpha thalassemia but not of patients with beta-thalassemia. These findings demonstrate differences in the degree of ineffective erythropoiesis in thalassemia, which emphasizes the need for different treatment approaches among patients with different thalassemia genotypes. AJTR
Copyright © 2022.

Entities:  

Keywords:  Phosphatidylserine exposed red blood cells; ineffective erythropoiesis biomarkers; thalassemia

Year:  2022        PMID: 35958503      PMCID: PMC9360869     

Source DB:  PubMed          Journal:  Am J Transl Res        ISSN: 1943-8141            Impact factor:   3.940


  34 in total

1.  Extramedullary haematopoiesis correlates with genotype and absence of cardiac iron overload in polytransfused adults with thalassaemia.

Authors:  Paolo Ricchi; Massimiliano Ammirabile; Anna Spasiano; Silvia Costantini; Tiziana Di Matola; Alessia Pepe; Patrizia Cinque; Leonilde Pagano; Maddalena Casale; Aldo Filosa; Luciano Prossomariti
Journal:  Blood Transfus       Date:  2013-10-03       Impact factor: 3.443

Review 2.  The hypercoagulable state in thalassemia.

Authors:  Amiram Eldor; Eliezer A Rachmilewitz
Journal:  Blood       Date:  2002-01-01       Impact factor: 22.113

3.  Elevations of Thrombotic Biomarkers in Hemoglobin H Disease.

Authors:  Siriyakorn Chansai; Supan Fucharoen; Goonnapa Fucharoen; Arunee Jetsrisuparb; Worawan Chumpia
Journal:  Acta Haematol       Date:  2018-01-18       Impact factor: 2.195

4.  Erythropoiesis-driven regulation of hepcidin in human red cell disorders is better reflected through concentrations of soluble transferrin receptor rather than growth differentiation factor 15.

Authors:  Kleber Yotsumoto Fertrin; Carolina Lanaro; Carla Fernanda Franco-Penteado; Dulcinéia Martins de Albuquerque; Mariana Rezende Bandeira de Mello; Flávia Rubia Pallis; Marcos André Cavalcanti Bezerra; Betania Lucena Domingues Hatzlhofer; Gordana Olbina; Sara Terezinha Olalla Saad; Aderson da Silva Araújo; Mark Westerman; Fernando Ferreira Costa
Journal:  Am J Hematol       Date:  2014-04       Impact factor: 10.047

5.  Levels of growth differentiation factor-15 are high and correlate with clinical severity in transfusion-independent patients with β thalassemia intermedia.

Authors:  Khaled M Musallam; Ali T Taher; Lorena Duca; Claudia Cesaretti; Racha Halawi; Maria Domenica Cappellini
Journal:  Blood Cells Mol Dis       Date:  2011-08-23       Impact factor: 3.039

6.  Splenectomy and thrombosis: the case of thalassemia intermedia.

Authors:  A T Taher; K M Musallam; M Karimi; A El-Beshlawy; K Belhoul; S Daar; M Saned; C Cesaretti; M D Cappellini
Journal:  J Thromb Haemost       Date:  2010-10       Impact factor: 5.824

7.  A correlation of erythrokinetics, ineffective erythropoiesis, and erythroid precursor apoptosis in thai patients with thalassemia.

Authors:  P Pootrakul; P Sirankapracha; S Hemsorach; W Moungsub; R Kumbunlue; A Piangitjagum; P Wasi; L Ma; S L Schrier
Journal:  Blood       Date:  2000-10-01       Impact factor: 22.113

8.  Erythropoiesis and Iron Homeostasis in Non-Transfusion-Dependent Thalassemia Patients with Extramedullary Hematopoiesis.

Authors:  Yumei Huang; Rongrong Liu; Xiaoyun Wei; Jiaodi Liu; Lingyuan Pan; Gaohui Yang; Yongrong Lai
Journal:  Biomed Res Int       Date:  2019-01-30       Impact factor: 3.411

9.  Imbalance of erythropoiesis and iron metabolism in patients with thalassemia.

Authors:  Yumei Huang; Yu Lei; Rongrong Liu; Jiaodi Liu; Gaohui Yang; Zhifu Xiang; Yuzhen Liang; Yongrong Lai
Journal:  Int J Med Sci       Date:  2019-01-01       Impact factor: 3.738

10.  Benefits of chronic blood transfusion in hemoglobin E/β thalassemia with pulmonary arterial hypertension.

Authors:  Nonlawan Chueamuangphan; Jayanton Patumanond; Wattana Wongtheptien; Weerasak Nawarawong; Apichard Sukonthasarn; Suporn Chuncharunee; Chamaiporn Tawichasri
Journal:  Int J Gen Med       Date:  2014-08-19
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.