Publication:
Micromapping of Thalassemia and Hemoglobinopathies Among Laos, Khmer, Suay and Yer Ethnic Groups Residing in Lower Northeastern Thailand

dc.contributor.authorRoongnalin Bunthupanichen_US
dc.contributor.authorRossarin Karnpeanen_US
dc.contributor.authorAnuwat Pinyachaten_US
dc.contributor.authorNawinda Jiambunsrien_US
dc.contributor.authorNattapol Prakobkaewen_US
dc.contributor.authorNaruwat Pakdeeen_US
dc.contributor.authorSupan Fucharoenen_US
dc.contributor.authorSuthat Fucharoenen_US
dc.contributor.otherRajamangala University of Technology Isanen_US
dc.contributor.otherUbon Ratchathani Universityen_US
dc.contributor.otherKhon Kaen Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherBurapha Universityen_US
dc.date.accessioned2020-08-25T09:06:49Z
dc.date.available2020-08-25T09:06:49Z
dc.date.issued2020-05-03en_US
dc.description.abstract© 2020 Informa UK Limited, trading as Taylor & Francis Group. Northeastern (NE) Thailand is one of the areas with a prevalence of thalassemias and hemoglobinopathies. Data on the prevalence of the diseases in minorities in the region has been limited. This study aimed to survey the thalassemias and hemoglobinopathies that take into account ethnicity. Four ethnic groups, including Laos (n = 162), Khmer (n = 145), Suay (n = 134), and Yer (n = 101) inhabiting the lower region of NE Thailand, were selected to represent the study populations. The results demonstrated that an extremely high prevalence of Hb E (HBB: c.79G>A) (>50.0%) was observed in the Khmer, Suay and Yer ethnic groups. The highest prevalence of α+-thalassemia (α+-thal) [–α3.7 (rightward)] deletion was found in the Khmer ethnic group (48.28%). The –α4.2 (leftward) deletion (α+-thal) was restricted to the Yer ethnic group. Yer and Suay had a high incidence of Hb Constant Spring (Hb CS; HBA2: c.427T>C) as well as Hb Paksé (HBA2: c.429A>T). As the prevalence of α0-thalassemia (α0-thal) is relatively high in Suay (7.46%), couples who are members of Suay ethnic population should be urged to undergo hematological screening before planning a pregnancy to control the Hb Bart’s hydrops fetalis. Micromapping of thalassemias and hemoglobinopathies herein described will be helpful in genetic counseling and public education campaigns, which should be carried out in appropriate languages, with exhibitions at the village levels. This information will be of benefit for the long-term effort to reduce the burden of severe thalassemia disease in the region.en_US
dc.identifier.citationHemoglobin. Vol.44, No.3 (2020), 162-167en_US
dc.identifier.doi10.1080/03630269.2020.1780252en_US
dc.identifier.issn1532432Xen_US
dc.identifier.issn03630269en_US
dc.identifier.other2-s2.0-85087165763en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/57734
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85087165763&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleMicromapping of Thalassemia and Hemoglobinopathies Among Laos, Khmer, Suay and Yer Ethnic Groups Residing in Lower Northeastern Thailanden_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85087165763&origin=inwarden_US

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