High Prevalence of Rare Mutations in the Beta Globin Gene in an Ethnic Group in Iran

Dear Editor, Beta Thalassemia major is a genetic disease with an autosomal recessive pattern and is differentiated by severe microcytic hypochromic hemolytic anemia with hepatosplenomegaly, ineffective erythropoiesis and bone marrow expansion. The β-globin (HBB) gene coding for β-chain expression is located on a 50 kb globin gene cluster on the short arm of chromosome 11, whose mutation mediated inactivation is usually responsive for the outcome of disease. Beta thalassemia occurs frequently in the coastline areas of the world. The Iran, with approximately 25000 beta thalassemia major patients and two millions expected carriers and an overall carrier frequency of 4-8%, counts to the Middle East countries with the highest prevalence of beta thalassemia. The Khuzestan Province in the southwest Iran with approximately 4.000.000 inhabitants ranks to the regions with the higher prevalence of the beta thalassemia, the most common type of hemoglobinopathies in Iran. Moreover, the cities Eizeh with nearly 120.000 and BaqMalek with 25.000 citizens are located in the North Khuzestan and are categorized to the small cities with relatively high carriers of the beta thalassemia. In the last decade, numerous studies have been published about distribution and frequency of mutations within the HBB gene in some regions of the Iran. These data were used to manage and provide a country-wide network for detecting beta thalassemia carrier and major individuals, which need intensive medical care. Nowadays, there are centers with special task to perform prenatal molecular diagnosis of the beta thalassemia in Iran with the goal to radically reduce the transfusion dependent beta thalassemia patients. However, the success of such centers is depending on the expanding knowledge about the kind and the continuation of pathogenic mutations within the ethnic groups in different area of the country. We firstly attempted also to fully analyze the beta globin gene in 130 blood transfusion dependent individuals in the two closely located towns, namely Eizeh and Baq-malek, After investigation a cohort of 200 beta thalassemia major patients and more than 1000 carriers in the Khuzestan Province in a previous study, where we showed more than 40 mutations within different ethnic groups in the province. Currently, we would know, whether the pure ethnic group such as Bakhtiari suggests similar frequency and distribution of mutations in the HBB gene as the province-wide study indicated. A total of 260 beta-globin alleles resulting from 130 blood transfusion-dependent patients (beta thalassemia major) were studied. All of analyzed patients belonged to the Bakhtiari ethnicity. Full sequencing of the beta globin gene in the subjected individuals revealed 15 β-thalassemia causing mutations as have been listed in the Table1. Fifty eight patients were homozygous and 72 patients were compound heterozygous for mutations. The seven most frequent mutations constituted 83.92% of all mutations. The mutations CD36/37(-T) and the IVS-II-1 were with 22.70% and 19.23% the most common mutations, accordinely. In addition, we found in 11.53% of cases (No=30), the mutation 5UTR+20 in association with the IVSII745 on one allele ( in cis) either compound with the 3 mutation on the second allele (N=12) or in hemozygous manner (in 9 cases; N=18). The beta thalassemia major individuals were also subjected for screening of the HBB gene in the two neighboring cities in the north-east Khuzestan Province because of some reasons; both cities harbor the ethnic group “Bakhtiari” with less than 300.000 inhabitants, which show relatively high prevalence of beta thalassemia carriers. Comparative studies were performed from different provinces in the Iran, but just few investigations were particularly based on the ethnic groups (e.g. Arab, Tork, Lor, etc.). In general, a minor part of thalassemia mutations predominant for geographic regions or countries. We showed in a previous province-wide study more than 40 mutations and in the present study 14 different mutations with similar trends regarding the distribution and the frequency. In contrast, we did find a mutation at 5UTR (+20) with more than 11%, which was reported in the province and in the country-wide study with 1% as a rarely event. According to the previous reports, the mentioned mutation occur usually in cis with the mutation IVSII-745(C>G) and the most prevalence of the mentioned mutation was reArchive of SID