Evaluation of serum vascular cell adhesion marker-1 in β- thalassemia major patients
BACKGROUND: Defects in the production of one or more hemoglobin chains result in a set of hereditary hematologic illnesses known as thalassemias. Alpha and β-thalassemia are the two primary thalassemia classifications. The pathophysiology of β-thalassemia is significantly influenced by endothelial a...
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Published in | Iraqi Journal of Hematology Vol. 14; no. 1; pp. 81 - 87 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
India
Wolters Kluwer - Medknow
2025
Medknow Publications and Media Pvt. Ltd Wolters Kluwer Medknow Publications |
Edition | 2 |
Subjects | |
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Abstract | BACKGROUND:
Defects in the production of one or more hemoglobin chains result in a set of hereditary hematologic illnesses known as thalassemias. Alpha and β-thalassemia are the two primary thalassemia classifications. The pathophysiology of β-thalassemia is significantly influenced by endothelial activation markers, such as vascular cell adhesion molecule 1 (VCAM-1), which have been found to be higher in both transfusion-dependent and nontransfusion-dependent thalassemia patients. These markers have been suggested for the follow-up of vascular disease in this patient group.
OBJECTIVES:
The aim of this study was to evaluate the level of soluble VCAM-1 in β-thalassemia major patients and to correlate its level with the clinical parameters.
PATIENTS, MATERIALS AND METHODS:
This case-control study was enrolled on 40 patients with β-thalassemia major. They were collected from Thalassemia Center of Babylon Maternity and Pediatrics Teaching Hospital, from December 28, 2022, to March 30, 2023. Twenty of them were splenectomized, others were not. Another 40 apparently healthy individuals with no family history of thalassemia or other hemoglobinopathy were enrolled in this study as controls. The samples were collected to assay the human VCAM-1 using enzyme-linked immunosorbent assay based on the biotin double antibody sandwich technology.
RESULTS:
Among 80 subjects, age and body mass index were similar across groups. There are differences in complete blood count (CBC) parameters between thalassemic and control groups. Thalassemic patients displayed notably higher levels of VCAM-1 and ferritin compared to controls and in splenectomized patients than nonsplenectomized patients. There is a high significant correlation exists between VCAM-1 and ferritin, VCAM-1 and various CBC parameters.
CONCLUSIONS:
There are higher levels of VCAM-1 in β-thalassemia major patients compared to the control and in splenectomized compared to non-splenectomized patients which usually associated with disease complications, furthermore it reflect endothelial activation and dysfunction. |
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AbstractList | BACKGROUND: Defects in the production of one or more hemoglobin chains result in a set of hereditary hematologic illnesses known as thalassemias. Alpha and β-thalassemia are the two primary thalassemia classifications. The pathophysiology of β-thalassemia is significantly influenced by endothelial activation markers, such as vascular cell adhesion molecule 1 (VCAM-1), which have been found to be higher in both transfusion-dependent and nontransfusion-dependent thalassemia patients. These markers have been suggested for the follow-up of vascular disease in this patient group. OBJECTIVES: The aim of this study was to evaluate the level of soluble VCAM-1 in β-thalassemia major patients and to correlate its level with the clinical parameters. PATIENTS, MATERIALS AND METHODS: This case-control study was enrolled on 40 patients with β-thalassemia major. They were collected from Thalassemia Center of Babylon Maternity and Pediatrics Teaching Hospital, from December 28, 2022, to March 30, 2023. Twenty of them were splenectomized, others were not. Another 40 apparently healthy individuals with no family history of thalassemia or other hemoglobinopathy were enrolled in this study as controls. The samples were collected to assay the human VCAM-1 using enzyme-linked immunosorbent assay based on the biotin double antibody sandwich technology. RESULTS: Among 80 subjects, age and body mass index were similar across groups. There are differences in complete blood count (CBC) parameters between thalassemic and control groups. Thalassemic patients displayed notably higher levels of VCAM-1 and ferritin compared to controls and in splenectomized patients than nonsplenectomized patients. There is a high significant correlation exists between VCAM-1 and ferritin, VCAM-1 and various CBC parameters. CONCLUSIONS: There are higher levels of VCAM-1 in β-thalassemia major patients compared to the control and in splenectomized compared to non-splenectomized patients which usually associated with disease complications, furthermore it reflect endothelial activation and dysfunction. Keywords: Splenectomized, vascular cell adhesion molecule 1, β-thalassemia major BACKGROUND: Defects in the production of one or more hemoglobin chains result in a set of hereditary hematologic illnesses known as thalassemias. Alpha and β-thalassemia are the two primary thalassemia classifications. The pathophysiology of β-thalassemia is significantly influenced by endothelial activation markers, such as vascular cell adhesion molecule 1 (VCAM-1), which have been found to be higher in both transfusion-dependent and nontransfusion-dependent thalassemia patients. These markers have been suggested for the follow-up of vascular disease in this patient group. OBJECTIVES: The aim of this study was to evaluate the level of soluble VCAM-1 in β-thalassemia major patients and to correlate its level with the clinical parameters. PATIENTS, MATERIALS AND METHODS: This case-control study was enrolled on 40 patients with β-thalassemia major. They were collected from Thalassemia Center of Babylon Maternity and Pediatrics Teaching Hospital, from December 28, 2022, to March 30, 2023. Twenty of them were splenectomized, others were not. Another 40 apparently healthy individuals with no family history of thalassemia or other hemoglobinopathy were enrolled in this study as controls. The samples were collected to assay the human VCAM-1 using enzyme-linked immunosorbent assay based on the biotin double antibody sandwich technology. RESULTS: Among 80 subjects, age and body mass index were similar across groups. There are differences in complete blood count (CBC) parameters between thalassemic and control groups. Thalassemic patients displayed notably higher levels of VCAM-1 and ferritin compared to controls and in splenectomized patients than nonsplenectomized patients. There is a high significant correlation exists between VCAM-1 and ferritin, VCAM-1 and various CBC parameters. CONCLUSIONS: There are higher levels of VCAM-1 in β-thalassemia major patients compared to the control and in splenectomized compared to non-splenectomized patients which usually associated with disease complications, furthermore it reflect endothelial activation and dysfunction. Defects in the production of one or more hemoglobin chains result in a set of hereditary hematologic illnesses known as thalassemias. Alpha and β-thalassemia are the two primary thalassemia classifications. The pathophysiology of β-thalassemia is significantly influenced by endothelial activation markers, such as vascular cell adhesion molecule 1 (VCAM-1), which have been found to be higher in both transfusion-dependent and nontransfusion-dependent thalassemia patients. These markers have been suggested for the follow-up of vascular disease in this patient group. The aim of this study was to evaluate the level of soluble VCAM-1 in β-thalassemia major patients and to correlate its level with the clinical parameters. This case-control study was enrolled on 40 patients with β-thalassemia major. They were collected from Thalassemia Center of Babylon Maternity and Pediatrics Teaching Hospital, from December 28, 2022, to March 30, 2023. Twenty of them were splenectomized, others were not. Another 40 apparently healthy individuals with no family history of thalassemia or other hemoglobinopathy were enrolled in this study as controls. The samples were collected to assay the human VCAM-1 using enzyme-linked immunosorbent assay based on the biotin double antibody sandwich technology. Among 80 subjects, age and body mass index were similar across groups. There are differences in complete blood count (CBC) parameters between thalassemic and control groups. Thalassemic patients displayed notably higher levels of VCAM-1 and ferritin compared to controls and in splenectomized patients than nonsplenectomized patients. There is a high significant correlation exists between VCAM-1 and ferritin, VCAM-1 and various CBC parameters. There are higher levels of VCAM-1 in β-thalassemia major patients compared to the control and in splenectomized compared to non-splenectomized patients which usually associated with disease complications, furthermore it reflect endothelial activation and dysfunction. BACKGROUND: Defects in the production of one or more hemoglobin chains result in a set of hereditary hematologic illnesses known as thalassemias. Alpha and β-thalassemia are the two primary thalassemia classifications. The pathophysiology of β-thalassemia is significantly influenced by endothelial activation markers, such as vascular cell adhesion molecule 1 (VCAM-1), which have been found to be higher in both transfusion-dependent and nontransfusion-dependent thalassemia patients. These markers have been suggested for the follow-up of vascular disease in this patient group. OBJECTIVES: The aim of this study was to evaluate the level of soluble VCAM-1 in β-thalassemia major patients and to correlate its level with the clinical parameters. PATIENTS, MATERIALS AND METHODS: This case–control study was enrolled on 40 patients with β-thalassemia major. They were collected from Thalassemia Center of Babylon Maternity and Pediatrics Teaching Hospital, from December 28, 2022, to March 30, 2023. Twenty of them were splenectomized, others were not. Another 40 apparently healthy individuals with no family history of thalassemia or other hemoglobinopathy were enrolled in this study as controls. The samples were collected to assay the human VCAM-1 using enzyme-linked immunosorbent assay based on the biotin double antibody sandwich technology. RESULTS: Among 80 subjects, age and body mass index were similar across groups. There are differences in complete blood count (CBC) parameters between thalassemic and control groups. Thalassemic patients displayed notably higher levels of VCAM-1 and ferritin compared to controls and in splenectomized patients than nonsplenectomized patients. There is a high significant correlation exists between VCAM-1 and ferritin, VCAM-1 and various CBC parameters. CONCLUSIONS: There are higher levels of VCAM-1 in β-thalassemia major patients compared to the control and in splenectomized compared to non-splenectomized patients which usually associated with disease complications, furthermore it reflect endothelial activation and dysfunction. |
Audience | Academic |
Author | Al-Mudallal, Subh Salim Al-Sarai, Nuha Abd Ali Najm, Rana Rai'd |
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Cites_doi | 10.1088/1742-6596/1294/6/062078 10.3390/ijns5010016 10.1080/00365510601051532 10.1002/jcla.22647 10.3109/03630260903347526 10.1002/mgg3.1788 10.1378/chest.10-0317 10.1007/s12687-016-0273-5 10.1002/ajh.20016 10.1056/NEJMra050436 10.4103/MJBL.MJBL_68_21 10.1055/s-0038-1649879 10.1111/j.1365-2141.2009.08054.x |
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References_xml | – volume: 1294 year: 2019 ident: R3-20250606 article-title: Investigating Some of Blood Parameters in Women with β-Thalassemia publication-title: J Phys Conf Ser doi: 10.1088/1742-6596/1294/6/062078 – volume: 5 start-page: 16 year: 2019 ident: R5-20250606 article-title: Thalassemias:An overview publication-title: Int J Neonatal Screen doi: 10.3390/ijns5010016 – volume: 67 start-page: 1 year: 2007 ident: R16-20250606 article-title: Current trends in the diagnosis and management of haemoglobinopathies publication-title: Scand J Clin Lab Invest doi: 10.1080/00365510601051532 – year: 2021 ident: R17-20250606 article-title: Williams Hematology publication-title: McGraw Hill / Medical – volume: 33 start-page: e22647 year: 2019 ident: R6-20250606 article-title: Laboratory diagnosis for thalassemia intermedia:Are we there yet? publication-title: J Clin Lab Anal doi: 10.1002/jcla.22647 – volume: 33 start-page: S81 issue: Suppl 1 year: 2009 ident: R18-20250606 article-title: Cardiac complications in thalassemia major publication-title: Hemoglobin doi: 10.3109/03630260903347526 – volume: 9 start-page: e1788 year: 2021 ident: R4-20250606 article-title: Current status of beta-thalassemia and its treatment strategies publication-title: Mol Genet Genomic Med doi: 10.1002/mgg3.1788 – volume: 138 start-page: 973 year: 2010 ident: R14-20250606 article-title: Pulmonary complications of hemoglobinopathies publication-title: Chest doi: 10.1378/chest.10-0317 – volume: 7 start-page: 243 year: 2016 ident: R15-20250606 article-title: Carrier screening for beta-thalassemia in the Maldives:Perceptions of parents of affected children who did not take part in screening and its consequences publication-title: J Community Genet doi: 10.1007/s12687-016-0273-5 – volume: 13 start-page: 1 year: 2017 ident: R13-20250606 article-title: Identification of the immunological profile in some Egyptian children with b-thalassemia major under different treatment modalities in El Minia Region publication-title: Immunome Res – volume: 76 start-page: 57 year: 2004 ident: R11-20250606 article-title: Elevated plasma sVCAM-1 levels in children with sickle cell disease:Impact of chronic transfusion therapy publication-title: Am J Hematol doi: 10.1002/ajh.20016 – volume: 353 start-page: 1135 year: 2005 ident: R12-20250606 article-title: Beta-thalassemia publication-title: N Engl J Med doi: 10.1056/NEJMra050436 – volume: 18 start-page: 410 year: 2021 ident: R1-20250606 article-title: Evaluation of thrombin activatable fibrinolysis inhibitor (TAFI) in patients with β-thalassemia publication-title: Med J Babylon doi: 10.4103/MJBL.MJBL_68_21 – volume: 74 start-page: 1045 year: 1995 ident: R9-20250606 article-title: Alterations in vascular endothelial cell-related plasma proteins in thalassaemic patients and their correlation with clinical symptoms publication-title: Thromb Haemost doi: 10.1055/s-0038-1649879 – volume: 149 start-page: 35 year: 2010 ident: R10-20250606 article-title: Significant haemoglobinopathies:Guidelines for screening and diagnosis publication-title: Br J Haematol doi: 10.1111/j.1365-2141.2009.08054.x |
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Snippet | BACKGROUND:
Defects in the production of one or more hemoglobin chains result in a set of hereditary hematologic illnesses known as thalassemias. Alpha and... BACKGROUND: Defects in the production of one or more hemoglobin chains result in a set of hereditary hematologic illnesses known as thalassemias. Alpha and... Defects in the production of one or more hemoglobin chains result in a set of hereditary hematologic illnesses known as thalassemias. Alpha and β-thalassemia... |
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SubjectTerms | Cell adhesion Evaluation Health aspects Original Article Physiological aspects splenectomized Thalassemia vascular cell adhesion molecule 1 β-thalassemia major |
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Title | Evaluation of serum vascular cell adhesion marker-1 in β- thalassemia major patients |
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