Hematological parameters and red blood cell morphological abnormality of Glucose-6-Phosphate dehydrogenase deficiency co-inherited with thalassemia
Objective/Background: Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency and thalassemia are genetically independent hemolytic disorders. Co-inheritance of both disorders may affect red blood cell pathology to a greater extent than normally seen in either disorder alone. This study determines the...
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doaj-7bd8188a73c84886a24b8b623fb750aa2020-11-25T02:14:10ZengElsevierHematology/Oncology and Stem Cell Therapy1658-38762018-03-011111824Hematological parameters and red blood cell morphological abnormality of Glucose-6-Phosphate dehydrogenase deficiency co-inherited with thalassemiaJutharat Pengon0Saovaros Svasti1Sumalee Kamchonwongpaisan2Phantip Vattanaviboon3Department of Clinical Microscopy, Faculty of Medical Technology, Mahidol University, Bangkok, Thailand; Medical Molecular Biology Research Unit, BIOTEC, National Science and Technology Development Agency, Pathum Thani, ThailandThalassemia Research Centre, Institute of Molecular Biosciences, Mahidol University, Nakhon Pathom, ThailandMedical Molecular Biology Research Unit, BIOTEC, National Science and Technology Development Agency, Pathum Thani, Thailand; Corresponding authors at: Department of Clinical Microscopy, Faculty of Medical Technology, Mahidol University, Bangkok 10700, Thailand (P. Vattanaviboon). Medical Molecular Biology Research Unit, BIOTEC, National Science and Technology Development Agency, Pathum Thani 12120, Thailand (S. Kamchonwongpaisan).Department of Clinical Microscopy, Faculty of Medical Technology, Mahidol University, Bangkok, Thailand; Corresponding authors at: Department of Clinical Microscopy, Faculty of Medical Technology, Mahidol University, Bangkok 10700, Thailand (P. Vattanaviboon). Medical Molecular Biology Research Unit, BIOTEC, National Science and Technology Development Agency, Pathum Thani 12120, Thailand (S. Kamchonwongpaisan).Objective/Background: Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency and thalassemia are genetically independent hemolytic disorders. Co-inheritance of both disorders may affect red blood cell pathology to a greater extent than normally seen in either disorder alone. This study determines the prevalence and evaluates hematological changes of G-6-PD deficiency and thalassemia co-inheritance. Methods: G-6-PD deficiency was screened from 200 male thalassemia blood samples using a fluorescent spot test. Hematological parameters and red blood cell morphology were evaluated among G-6-PD deficiency/thalassemia co-inheritance, G-6-PD deficiency alone, thalassemia alone, and normal individuals. Results: G-6-PD deficiency was detected together with hemoglobin (Hb) E heterozygote, Hb E homozygote, β-thalassemia trait, and β-thalassemia/Hb E, α-thalassemia-2 trait, and Hb H disease. Hb level, hematocrit, mean cell volume, and mean cell Hb of G-6-PD deficiency co-inherited with asymptomatic thalassemia carriers show significantly lower mean values compared to carriers with only the same thalassemia genotypes. Higher mean red blood cell distribution width was observed in G-6-PD deficiency co-inherited with Hb E heterozygote, as with numbers of hemighost cells in G-6-PD deficiency/thalassemia co-inheritance compared to those with either disorder. Apart from Hb level, hematological parameters of co-inheritance disorders were not different from individuals with a single thalassemia disease. Conclusion: G-6-PD deficiency co-inherited with thalassemia in males was present in 10% of the participants, resulting in worsening of red blood cell pathology compared with inheritance of thalassemia alone. Keywords: G-6-PD deficiency, Red blood cell morphology, Red blood cell parameters, Thalassemiahttp://www.sciencedirect.com/science/article/pii/S1658387617300845 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jutharat Pengon Saovaros Svasti Sumalee Kamchonwongpaisan Phantip Vattanaviboon |
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Jutharat Pengon Saovaros Svasti Sumalee Kamchonwongpaisan Phantip Vattanaviboon Hematological parameters and red blood cell morphological abnormality of Glucose-6-Phosphate dehydrogenase deficiency co-inherited with thalassemia Hematology/Oncology and Stem Cell Therapy |
author_facet |
Jutharat Pengon Saovaros Svasti Sumalee Kamchonwongpaisan Phantip Vattanaviboon |
author_sort |
Jutharat Pengon |
title |
Hematological parameters and red blood cell morphological abnormality of Glucose-6-Phosphate dehydrogenase deficiency co-inherited with thalassemia |
title_short |
Hematological parameters and red blood cell morphological abnormality of Glucose-6-Phosphate dehydrogenase deficiency co-inherited with thalassemia |
title_full |
Hematological parameters and red blood cell morphological abnormality of Glucose-6-Phosphate dehydrogenase deficiency co-inherited with thalassemia |
title_fullStr |
Hematological parameters and red blood cell morphological abnormality of Glucose-6-Phosphate dehydrogenase deficiency co-inherited with thalassemia |
title_full_unstemmed |
Hematological parameters and red blood cell morphological abnormality of Glucose-6-Phosphate dehydrogenase deficiency co-inherited with thalassemia |
title_sort |
hematological parameters and red blood cell morphological abnormality of glucose-6-phosphate dehydrogenase deficiency co-inherited with thalassemia |
publisher |
Elsevier |
series |
Hematology/Oncology and Stem Cell Therapy |
issn |
1658-3876 |
publishDate |
2018-03-01 |
description |
Objective/Background: Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency and thalassemia are genetically independent hemolytic disorders. Co-inheritance of both disorders may affect red blood cell pathology to a greater extent than normally seen in either disorder alone. This study determines the prevalence and evaluates hematological changes of G-6-PD deficiency and thalassemia co-inheritance. Methods: G-6-PD deficiency was screened from 200 male thalassemia blood samples using a fluorescent spot test. Hematological parameters and red blood cell morphology were evaluated among G-6-PD deficiency/thalassemia co-inheritance, G-6-PD deficiency alone, thalassemia alone, and normal individuals. Results: G-6-PD deficiency was detected together with hemoglobin (Hb) E heterozygote, Hb E homozygote, β-thalassemia trait, and β-thalassemia/Hb E, α-thalassemia-2 trait, and Hb H disease. Hb level, hematocrit, mean cell volume, and mean cell Hb of G-6-PD deficiency co-inherited with asymptomatic thalassemia carriers show significantly lower mean values compared to carriers with only the same thalassemia genotypes. Higher mean red blood cell distribution width was observed in G-6-PD deficiency co-inherited with Hb E heterozygote, as with numbers of hemighost cells in G-6-PD deficiency/thalassemia co-inheritance compared to those with either disorder. Apart from Hb level, hematological parameters of co-inheritance disorders were not different from individuals with a single thalassemia disease. Conclusion: G-6-PD deficiency co-inherited with thalassemia in males was present in 10% of the participants, resulting in worsening of red blood cell pathology compared with inheritance of thalassemia alone. Keywords: G-6-PD deficiency, Red blood cell morphology, Red blood cell parameters, Thalassemia |
url |
http://www.sciencedirect.com/science/article/pii/S1658387617300845 |
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