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A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration

BACKGROUND: Hemoglobin (Hb) variants are structurally inherited changes of globin chains. Accurate diagnoses of these variants are important for planning of appropriate management and genetic counseling. Since no epidemiological study has been conducted before, we have investigated frequencies, mole...

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Autores principales: Srivorakun, Hataichanok, Singha, Kritsada, Fucharoen, Goonnapa, Sanchaisuriya, Kanokwan, Fucharoen, Supan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171515/
https://www.ncbi.nlm.nih.gov/pubmed/25244406
http://dx.doi.org/10.1371/journal.pone.0108365
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author Srivorakun, Hataichanok
Singha, Kritsada
Fucharoen, Goonnapa
Sanchaisuriya, Kanokwan
Fucharoen, Supan
author_facet Srivorakun, Hataichanok
Singha, Kritsada
Fucharoen, Goonnapa
Sanchaisuriya, Kanokwan
Fucharoen, Supan
author_sort Srivorakun, Hataichanok
collection PubMed
description BACKGROUND: Hemoglobin (Hb) variants are structurally inherited changes of globin chains. Accurate diagnoses of these variants are important for planning of appropriate management and genetic counseling. Since no epidemiological study has been conducted before, we have investigated frequencies, molecular and hematological features of Hb variants found in a large cohort of Thai subjects. MATERIALS AND METHODS: Study was conducted on 26,013 unrelated subjects, inhabiting in all geographical parts of Thailand over a period of 11 years from January 2002-December 2012. Hb analysis was done on high performance liquid chromatography (HPLC) or capillary electrophoresis (CE). Mutations causing Hb variants were identified using PCR and related techniques. RESULTS: Among 26,013 subjects investigated, 636 (2.4%) were found to carry Hb variants. Of these 636 subjects, 142 (22.4%) carried α-chain variants with 13 different mutations. The remaining included 451 (70.9%) cases with 16 β-chain variants, 37 (5.8%) cases with Hb Lepore (δβ-hybrid Hb) and 6 (0.9%) cases with a single δ-chain variant. The most common α-globin chain variant was the Hb Q-Thailand (α(74GAC-CAC, Asp-His)) which was found in 101 cases (15.8%). For β-globin chain variants, Hb Hope (β(136GGT-GAT, Gly-Asp)) and Hb Tak (β(146+AC, Ter-Thr)) are the two most common ones, found in 121 (19.0%) and 90 (14.2%) cases, respectively. Seven Hb variants have never been found in Thai population. Hb analysis profiles on HPLC or CE of these variants were illustrated to guide presumptive diagnostics. CONCLUSIONS: Hb variants are common and heterogeneous in Thai population. With varieties of thalassemias and hemoglobinopathies in the population, interactions between them leading to complex syndromes are common and render their diagnoses difficult in routine practices. Knowledge of the spectrum, molecular basis, genotype-phenotype correlation and diagnostic features should prove useful for prevention and control of the diseases in the region.
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spelling pubmed-41715152014-09-25 A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration Srivorakun, Hataichanok Singha, Kritsada Fucharoen, Goonnapa Sanchaisuriya, Kanokwan Fucharoen, Supan PLoS One Research Article BACKGROUND: Hemoglobin (Hb) variants are structurally inherited changes of globin chains. Accurate diagnoses of these variants are important for planning of appropriate management and genetic counseling. Since no epidemiological study has been conducted before, we have investigated frequencies, molecular and hematological features of Hb variants found in a large cohort of Thai subjects. MATERIALS AND METHODS: Study was conducted on 26,013 unrelated subjects, inhabiting in all geographical parts of Thailand over a period of 11 years from January 2002-December 2012. Hb analysis was done on high performance liquid chromatography (HPLC) or capillary electrophoresis (CE). Mutations causing Hb variants were identified using PCR and related techniques. RESULTS: Among 26,013 subjects investigated, 636 (2.4%) were found to carry Hb variants. Of these 636 subjects, 142 (22.4%) carried α-chain variants with 13 different mutations. The remaining included 451 (70.9%) cases with 16 β-chain variants, 37 (5.8%) cases with Hb Lepore (δβ-hybrid Hb) and 6 (0.9%) cases with a single δ-chain variant. The most common α-globin chain variant was the Hb Q-Thailand (α(74GAC-CAC, Asp-His)) which was found in 101 cases (15.8%). For β-globin chain variants, Hb Hope (β(136GGT-GAT, Gly-Asp)) and Hb Tak (β(146+AC, Ter-Thr)) are the two most common ones, found in 121 (19.0%) and 90 (14.2%) cases, respectively. Seven Hb variants have never been found in Thai population. Hb analysis profiles on HPLC or CE of these variants were illustrated to guide presumptive diagnostics. CONCLUSIONS: Hb variants are common and heterogeneous in Thai population. With varieties of thalassemias and hemoglobinopathies in the population, interactions between them leading to complex syndromes are common and render their diagnoses difficult in routine practices. Knowledge of the spectrum, molecular basis, genotype-phenotype correlation and diagnostic features should prove useful for prevention and control of the diseases in the region. Public Library of Science 2014-09-22 /pmc/articles/PMC4171515/ /pubmed/25244406 http://dx.doi.org/10.1371/journal.pone.0108365 Text en © 2014 Srivorakun et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Srivorakun, Hataichanok
Singha, Kritsada
Fucharoen, Goonnapa
Sanchaisuriya, Kanokwan
Fucharoen, Supan
A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration
title A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration
title_full A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration
title_fullStr A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration
title_full_unstemmed A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration
title_short A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration
title_sort large cohort of hemoglobin variants in thailand: molecular epidemiological study and diagnostic consideration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4171515/
https://www.ncbi.nlm.nih.gov/pubmed/25244406
http://dx.doi.org/10.1371/journal.pone.0108365
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