Prevalence of Thalassemia Traits and Iron Deficiency Anemia in Sindh, Pakistan
- 4 May 2017
- journal article
- Published by Taylor & Francis in Hemoglobin
- Vol. 41 (3) , 157-163
Abstract
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.Keywords
Funding Information
- Mahidol University
- Thailand Research Fund (MRG5480062)
This publication has 19 references indexed in Scilit:
- RDW as differential parameter between microcytic anemias in “pure” and concomitant formsJornal Brasileiro de Patologia e Medicina Laboratorial, 2015
- ThalassemiasPediatric Clinics of North America, 2013
- Public perceptions and attitudes toward thalassaemia: Influencing factors in a multi-racial populationBMC Public Health, 2011
- Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western IndiaIndian Journal of Human Genetics, 2010
- Red blood cell microcytosis and hypochromia in the differential diagnosis of iron deficiency and β‐thalassaemia traitInternational Journal of Laboratory Hematology, 2009
- Molecular diagnosis of β‐thalassemia by multiplex ARMS‐PCR: a cost effective method for developing countries like PakistanPrenatal Diagnosis, 2007
- Thalassemia in IranJournal of Pediatric Hematology/Oncology, 2007
- Beta‐thalassaemia in the immigrant and non‐immigrant German populationsBritish Journal of Haematology, 1997
- Distribution of hemoglobinopathy variants by ethnicity in a multiethnic stateGenetic Epidemiology, 1996
- Hemoglobinopathies in Southeast AsiaHemoglobin, 1987