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dc.contributor.advisorMannoor, Md. Kaiissar
dc.contributor.advisorChoudhury, Naiyyum
dc.contributor.authorBiswas, Aparna
dc.date.accessioned2019-07-18T04:58:53Z
dc.date.available2019-07-18T04:58:53Z
dc.date.copyright2018
dc.date.issued2018-12
dc.identifier.otherID 16176003
dc.identifier.urihttp://hdl.handle.net/10361/12390
dc.descriptionThis thesis report is submitted in partial fulfilment of the requirement for the degree of Master of Science in Biotechnology, 2018.en_US
dc.descriptionCatalogued from PDF version of thesis.
dc.descriptionIncludes bibliographical references (pages 66-73).
dc.description.abstractβ-thalassemia and hemoglobin E (Hb E) diseases are highly prevalent autosomal recessive disorders characterized by the reduced or absent expression of the β globin gene. β-thalassemia is now regarded as the most common inherited single gene disorder in the world including Bangladesh. Like β-thalassemia, Hb E disorder is also supposed to be highly prevalent in Bangladesh. Around 4.1 % of total populations are carriers of beta thalassemia and 6.1% are carriers of Hemoglobin-E beta thalassemia (Hb-EBT) in Bangladesh. Around three hundred thousand infants are born with Thalassemia worldwide each year and more than 270 million people are carriers of Thalassemia. It has been estimated by Hardy-Weinberg equation that approximately 8990 beat-thalassemia babies are being born each year in Bangladesh. Individuals with beta-thalassemia major (BTM) suffer from severe anemia, growth retardation, splenomegaly, jaundice, expansion of bone-marrow, bone deformities and require blood transfusion to avoid complications. The aim of the present study is to identify the common mutations of beta-globin gene and to establish any possible correlation with hematological parameters and with blood transfusion interval of the patients which is the indicator of disease severity of the thalassemia patients. A total of 60 transfusion dependent thalassemia patients were enrolled for the study from Dhaka Shishu Hospital. Among these patients, 31 (51.7%) and 29 (48.3%) patients were males and females, respectively. Complete blood count (CBC) and Hb-electrophoresis were performed to identify the type of beta-thalassemia patients. The mutations of beta-globin gene were detected by amplification of selective region of beta-globin gene using polymerase chain reaction (PCR) followed by automated Sanger’s DNA sequencing and BLAST method. Among 60 transfusion dependent thalassemia patients, 39 (65%) were suffering from Hb-EBT (EBT), whereas 21 (35%) patients had beta thalassemia major (BTM). Mutation analysis of beta-globin gene revealed 9 mutations, namely c.79 G>A, IVS-1-5 G>C, c.126-129 del_CTTT, IVS-I-130 G>C, c.47 G>A, c.33 delA, c.51delC, c. G92C and c.126delC. Further, we found lower level of RBC count, hematocrit, MCV and MCH compared to the respective reference values, whereas the mean RDW level and WBC count of the enrolled patients were higher than the reference range. The enrolled patients were divided into three groups based on their transfusion intervals, namely Group 1 (< 1 month), Group 2 (1 month to < 1.5 month) and Group 3 (> 1.5 months). One-way ANOVA test for hematocrit, Hb concentration, RBC count, MCV, MCH, RDW and WBC count among these three groups of patients had been performed. We found no statistically significant difference among these three groups in terms of percentages of hematocrit (ANOVA: p = 0.9973), MCHC (ANOVA: p = 0.0605), MCV (ANOVA: p = 0.0782), platelet count (ANOVA: p = 0.9710), RBC count (ANOVA: p = 0.3954) and WBC count (ANOVA: p = 0.7415) but there was statistically significant difference in terms of MCH (ANOVA: p = 0.0319) and RDW (ANOVA: p = 0.0020) value between Group 1 and Group 3 in our study. In conclusion, the data from our study clearly demonstrates that group 3 (less severe group) patients had higher MCH and RDW values compared to the Group 1 patients (most severe group).en_US
dc.description.statementofresponsibilityAparna Biswas
dc.format.extent73 pages
dc.language.isoenen_US
dc.publisherBrac Universityen_US
dc.rightsBrac University theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission.
dc.subjectβ-thalassemiaen_US
dc.subjectHemoglobin Een_US
dc.subjectHBB gene mutationen_US
dc.subjectBeta thalassemia majoren_US
dc.subjectSplenomegalyen_US
dc.subjectComplete blood counten_US
dc.subjectTransfusion intervalen_US
dc.subject.lcshThalassemia--Diagnosis
dc.titleDetection of beta globin gene mutations in thalassemia patients in Bangladesh and correlation with hematological parametersen_US
dc.typeThesisen_US
dc.contributor.departmentDepartment of Mathematics and Natural Sciences, Brac University
dc.description.degreeM. Biotechnology


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