Molecular Epidemiology of Hemoglobinopathies in Cambodia
© 2016 Informa UK Limited, trading as Taylor & Francis Group. Determining the magnitude of the thalassemia problem in a country is important for implementing a national prevention and control program. In order to acquire accurate thalassemia prevalence data, the gene frequency of α- and β-thal...
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th-mahidol.430482019-03-14T15:04:06Z Molecular Epidemiology of Hemoglobinopathies in Cambodia Thongperm Munkongdee Jatuporn Tanakulmas Punnee Butthep Pranee Winichagoon Barbara Main Miriam Yiannakis Joby George Robyn Devenish Suthat Fucharoen Saovaros Svasti Mahidol University World Vision Canada World Vision Cambodia Laboratory Medicine Unlimited Biochemistry, Genetics and Molecular Biology © 2016 Informa UK Limited, trading as Taylor & Francis Group. Determining the magnitude of the thalassemia problem in a country is important for implementing a national prevention and control program. In order to acquire accurate thalassemia prevalence data, the gene frequency of α- and β-thalassemia (α- and β-thal) in different regions of a country should be determined. The molecular basis of thalassemia in Cambodia was performed by polymerase chain reaction (PCR)-based techniques in a community-based cross-sectional survey of 1631 unrelated individuals from three regions, Battambang, Preah Vihear and Phnom Penh. Thalassemia mutations were detected in 62.7% of the three studied population of Cambodia. Hb E (HBB: c.79G > A) was the most common β-globin gene mutation with a frequency ranging from 0.139 to 0.331, while the most frequent α-globin gene mutation was the -α3.7(rightward) deletion (0.098-0.255). The other frequencies were 0.001-0.003 for β-thal, 0.008-0.011 for α-thal-1 (- -SEA), 0.003-0.008 for α-thal-2 [-α4.2(leftward deletion)], 0.021-0.044 for Hb Constant Spring (Hb CS, HBA2: c.427T > C) and 0.009-0.036 for Hb Paksé (HBA2: c.429A > T). A regional specific thalassemia gene frequency was observed. Preah Vihear had the highest prevalence of Hb E (55.9%), α-thal-2 (24.0%) and nondeletional α-thal (15.1%), whereas Phnom Penh had the lowest frequency of thalassemia genes. Interestingly, in Preah Vihear, the frequency of Hb Paksé was extremely high (0.036), almost equivalent to that of Hb CS (0.044). Our results indicate the importance of micromapping and epidemiology studies of thalassemia, which will assist in establishing the national prevention and control program in Cambodia. 2018-12-11T02:15:43Z 2019-03-14T08:04:06Z 2018-12-11T02:15:43Z 2019-03-14T08:04:06Z 2016-05-03 Article Hemoglobin. Vol.40, No.3 (2016), 163-167 10.3109/03630269.2016.1158723 1532432X 03630269 2-s2.0-84971628902 https://repository.li.mahidol.ac.th/handle/123456789/43048 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84971628902&origin=inward |
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Biochemistry, Genetics and Molecular Biology Thongperm Munkongdee Jatuporn Tanakulmas Punnee Butthep Pranee Winichagoon Barbara Main Miriam Yiannakis Joby George Robyn Devenish Suthat Fucharoen Saovaros Svasti Molecular Epidemiology of Hemoglobinopathies in Cambodia |
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© 2016 Informa UK Limited, trading as Taylor & Francis Group. Determining the magnitude of the thalassemia problem in a country is important for implementing a national prevention and control program. In order to acquire accurate thalassemia prevalence data, the gene frequency of α- and β-thalassemia (α- and β-thal) in different regions of a country should be determined. The molecular basis of thalassemia in Cambodia was performed by polymerase chain reaction (PCR)-based techniques in a community-based cross-sectional survey of 1631 unrelated individuals from three regions, Battambang, Preah Vihear and Phnom Penh. Thalassemia mutations were detected in 62.7% of the three studied population of Cambodia. Hb E (HBB: c.79G > A) was the most common β-globin gene mutation with a frequency ranging from 0.139 to 0.331, while the most frequent α-globin gene mutation was the -α3.7(rightward) deletion (0.098-0.255). The other frequencies were 0.001-0.003 for β-thal, 0.008-0.011 for α-thal-1 (- -SEA), 0.003-0.008 for α-thal-2 [-α4.2(leftward deletion)], 0.021-0.044 for Hb Constant Spring (Hb CS, HBA2: c.427T > C) and 0.009-0.036 for Hb Paksé (HBA2: c.429A > T). A regional specific thalassemia gene frequency was observed. Preah Vihear had the highest prevalence of Hb E (55.9%), α-thal-2 (24.0%) and nondeletional α-thal (15.1%), whereas Phnom Penh had the lowest frequency of thalassemia genes. Interestingly, in Preah Vihear, the frequency of Hb Paksé was extremely high (0.036), almost equivalent to that of Hb CS (0.044). Our results indicate the importance of micromapping and epidemiology studies of thalassemia, which will assist in establishing the national prevention and control program in Cambodia. |
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Mahidol University |
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Mahidol University Thongperm Munkongdee Jatuporn Tanakulmas Punnee Butthep Pranee Winichagoon Barbara Main Miriam Yiannakis Joby George Robyn Devenish Suthat Fucharoen Saovaros Svasti |
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Article |
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Thongperm Munkongdee Jatuporn Tanakulmas Punnee Butthep Pranee Winichagoon Barbara Main Miriam Yiannakis Joby George Robyn Devenish Suthat Fucharoen Saovaros Svasti |
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Thongperm Munkongdee |
title |
Molecular Epidemiology of Hemoglobinopathies in Cambodia |
title_short |
Molecular Epidemiology of Hemoglobinopathies in Cambodia |
title_full |
Molecular Epidemiology of Hemoglobinopathies in Cambodia |
title_fullStr |
Molecular Epidemiology of Hemoglobinopathies in Cambodia |
title_full_unstemmed |
Molecular Epidemiology of Hemoglobinopathies in Cambodia |
title_sort |
molecular epidemiology of hemoglobinopathies in cambodia |
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2018 |
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https://repository.li.mahidol.ac.th/handle/123456789/43048 |
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1763491978647961600 |