Co-Inheritance of alpha-thalassemia and sickle cell disease in a cohort of Angolan pediatric patients

Brígida Santos, Mariana Delgadinho, Joana Ferreira, Isabel Germano, Armandina Miranda, Ana Paula Arez, Paula Faustino, Miguel Brito

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4 Citations (Scopus)


The aim of this study was to explore the association between alpha-thalassemia, fetal hemoglobin, hematological indices, and clinical adverse events in Angolan sickle cell disease pediatric patients. A total of 200 sickle cell disease (SCD) children were sampled in Luanda and Caxito. A venous blood sample was collected and used for hematological analyses, fetal hemoglobin quantification, and genotyping of 3.7 kb alpha-thalassemia deletion by GAP-PCR. The frequency of the 3.7 kb alpha-thalassemia deletion in homozygosity was 12.5% and in heterozygosity was 55.0%. An increase in alpha-thalassemia frequency was observed in children older than 5 years old (11.7% vs. 13.00%). Furthermore, 3.7 kb alpha-thalassemia deletion homozygotes had a significantly higher age of the first manifestation, lower number of blood transfusions by year, higher hemoglobin, lower mean corpuscular volume, mean corpuscular hemoglobin, and lower hemolytic rate observed by a lower number of reticulocytes count. There were no differences in fetal hemoglobin between the three genotypes. Moreover, the number of stroke events, osteomyelitis, splenomegaly, splenectomy, and hepatomegaly were lower when alpha-thalassemia was co-inherited. For the first time in Angolan population, the effect of alpha-thalassemia deletion in sickle cell disease was analyzed and results reinforce that this trait influences the hematological and clinical aspects and produces a milder phenotype.
Original languageEnglish
Pages (from-to)5397-5402
Number of pages6
JournalMolecular Biology Reports
Issue number7
Early online date6 Jul 2020
Publication statusPublished - Jul 2020


  • 3.7 kb alpha-thalassemia deletion
  • Fetal hemoglobin
  • Sickle cell disease
  • Angola


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