Title of article :
Prevalence of various mutations in beta thalassaemia and its association with haematological parameters
Author/Authors :
Khattak, Saeed Akhtar Khan Armed Forces Institute of Pathology - Department of Haematology, Pakistan , Ahmed, Suhaib Armed Forces Institute of Pathology - Department of Pathology, Pakistan , Anwar, Jaleel PNS Shifa - Department of Haematology, Pakistan , Ali, Nadir Armed Forces Institute of Pathology - Department of Pathology, Pakistan , Shaikh, Kashif Hafeez PAF Hospital - Department of Pathology, Pakistan
Abstract :
Objective: To determine the prevalence of various mutations in beta (b) thalassaemia and its association with haematological parameters.Methods: A descriptive cross sectional study was carried out in the Department of Haematology, Armed Forced Institute of Pathology (AFIP) from February 2009 to January 2010. A total of 515 carriers having b thalassaemia mutations characterized by Multiplex amplification refractory mutation system (ARMS) were included in the study. Frequencies of different b thalassaemia mutations were calculated. Mutations were analyzed for their haematological parameters which include total red blood cell count (TRBC), haemoglobin (Hb), mean cell volume (MCV), mean cell haemoglobin (MCH) and red cell distribution width (RDW).Results: Frame shift (Fr) 8-9 was the most common mutation found in 183 (35.5%) of patients followed by intervening sequence I-5 (IVSI-5) in 126 (24.5%) and Fr 41-42 in 76 (14.8%) while IVSII-1 was the least common mutation found in 1 patient. Fr 8-9 was also the commonest mutation in Punjabis and Pathans. Predominant mutation in other ethnic carriers was IVSI-5. Patients with Fr 8-9 mutation had the lowest mean MCV and MCH of 63.7fl and 19.1pg, of all the mutations. Patients with CAP+1 mutation had mean TRBC, Hb, MCV, MCH and RDW of 5.5 x 1012/L,13.5g/dl, 78.0fl, 24.7pg and 41.9fl respectively.Conclusion: Fr 8-9 is the most common b thalassaemia mutation with lowest red cell indices while CAP+1 mutation can present with normal red cell values therefore, a potential carrier should be screened for CAP+1 mutation by DNA analysis
Keywords :
Beta thalassaemia, Mutation and Haematological values (JPMA 62: 40 , 2012)
Journal title :
Journal of the Pakistan Medical Association (Centre) JPMA
Journal title :
Journal of the Pakistan Medical Association (Centre) JPMA