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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Main Authors: Jutharat Pengon, Saovaros Svasti, Sumalee Kamchonwongpaisan, Phantip Vattanaviboon
Format: Article
Language:English
Published: Elsevier 2018-03-01
Series:Hematology/Oncology and Stem Cell Therapy
Online Access:http://www.sciencedirect.com/science/article/pii/S1658387617300845
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spelling 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
spellingShingle 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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