| Literature DB >> 28361595 |
Paolo Gorello1, Francesco Arcioni2, Antonietta Palmieri3, Ylenia Barbanera1, Laura Ceccuzzi1, Cecilia Adami4, Mauro Marchesi5, Antonella Angius6, Olivia Minelli5, Marina Onorato5, Antonio Piga3, Maurizio Caniglia2, Cristina Mecucci1, Antonella Roetto3.
Abstract
The aim of this study was to describe the mutational spectrum of hemoglobinopathies during the period 1988-2015 in Umbria, Central Italy, which has never been considered endemic for these conditions. Twenty-four different β-globin gene mutations were identified in 188 patients and eight different α-globin gene mutations in 74 patients. Sixty percent β-thalassemia (β-thal), 85.0% sickle cell disease, 44.0% Hb S (HBB: c.20A>T)/β-thal and 85.0% compound heterozygotes for hemoglobin (Hb) variant-carrying patients were diagnosed or molecularly characterized in the last 3 years. Moreover, most homozygous or compound heterozygous patients (84.5%) came from foreign countries, while only 15.5% were of Italian origin. These data are in accordance with the increasing foreign resident population in Umbria, which has nearly doubled in 10 years (2004-2014). Different from β-globin gene variations, no increasing trend in α defects was observed in our study cohort. Consistently, 58.0% of patients have an Italian origin, suggesting no broad influence of foreign migration in the α-globin genes genetic background. As few defects are prevalent in each country of origin or ethnic group, their knowledge may provide a proper strategy for the identification of mutations in immigrant individuals in a non-endemic region and be important for carrier identification and prenatal screening.Entities:
Keywords: Hemoglobinopathies; Italy; hemoglobin (Hb) variants; sickle cell disease; thalassemias
Mesh:
Year: 2016 PMID: 28361595 DOI: 10.1080/03630269.2017.1289101
Source DB: PubMed Journal: Hemoglobin ISSN: 0363-0269 Impact factor: 0.849