Publication:
Prevalence of Thalassemia Traits and Iron Deficiency Anemia in Sindh, Pakistan

dc.contributor.authorAbdul H. Kandhroen_US
dc.contributor.authorVirapong Prachayasittikulen_US
dc.contributor.authorChartchalerm Isarankura Na-Ayudhyaen_US
dc.contributor.authorPornlada Nuchnoien_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-12-21T06:49:13Z
dc.date.accessioned2019-03-14T08:02:54Z
dc.date.available2018-12-21T06:49:13Z
dc.date.available2019-03-14T08:02:54Z
dc.date.issued2017-05-04en_US
dc.description.abstract© 2017 Informa UK Limited, trading as Taylor & Francis Group. Among microcytic hypochromic anemias, the most common disorders are iron deficiency anemia and co-pathological conditions such as α- or β-thalassemia (α- or β-thal) traits. The aim of the present study was to determine the frequency and prevalence of iron deficiency anemia and α- or β-thal traits based on clinical laboratory data across different ethnic groups in five districts of Sindh Province, Pakistan. The present retrospective study analyzed 3 years (2012–2015) of encoded and unlinked clinical laboratory data, and identified 3030 microcytic hypochromic anemia cases. The data contained complete blood counts (CBCs) with smear morphology examinations, serum ferritin levels, and hemoglobin (Hb) electrophoreses. After reviewing the data, 994 confirmed subjects (iron deficiency anemia and α- and β-thal traits) were then selected for the present study. The prevalence of α- and β-thal traits was highest in Badin district (35.27%), while the prevalence of iron deficiency anemia was highest in Larkana district (30.73%). According to the ethnic-wise distribution, higher numbers of α- and β-thal trait cases were seen in the Sindhi ethnic group [375 (64.21%) and 283 (69.02%), respectively] than in the other ethnic groups. In addition, a higher distribution of β-thal trait cases was observed in the Sindhi ethnic group [n = 327 (56%)] in α- and β-thal cases overall. Findings from the present study strongly suggested that screening is important not only for β-thal trait but also other traits as well. However, careful monitoring of CBC parameters, including red blood cell (RBC) indices and morphology, along with clinical findings are essential to diagnose carrier cases, especially in high prevalence areas.en_US
dc.identifier.citationHemoglobin. Vol.41, No.3 (2017), 157-163en_US
dc.identifier.doi10.1080/03630269.2017.1345759en_US
dc.identifier.issn1532432Xen_US
dc.identifier.issn03630269en_US
dc.identifier.other2-s2.0-85026225568en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/41896
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85026225568&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titlePrevalence of Thalassemia Traits and Iron Deficiency Anemia in Sindh, Pakistanen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85026225568&origin=inwarden_US

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