Literature DB >> 31596378

Prevalence of hemoglobinopathies in the Brazilian adult population: National Health Survey 2014-2015.

Luiz Gastão Rosenfeld1, Nydia Strachman Bacal1, Maria Alice Martins Cuder2, Alanna Gomes da Silva3, Ísis Eloah Machado3, Cimar Azereido Pereira4, Maria de Fátima Marinho de Souza5, Deborah Carvalho Malta6.   

Abstract

OBJECTIVE: To describe the prevalence of hemoglobinopathies in the Brazilian adult population, according to laboratory tests from the National Health Survey.
METHODS: A descriptive study was carried out with National Health Survey laboratory data collected between 2014 and 2015. The hemoglobinopathies test was performed using the High Performance Liquid Chromatography method. The results of the individual tests were interpreted as providing normal, homozygous or heterozygous results for S, C and D hemoglobin, in addition to other possible hemoglobinopathies. Prevalence of hemoglobinopathies according to gender, skin color, region, age and schooling was estimated.
RESULTS: Hemoglobinopathies were present in 3.7% of the population. The main ones were the sickle cell trait (2.49%), thalassemia minor (0.30%) and suspected thalassemia major (0.80%). In relation to the sickle cell trait and suspected thalassemia major, there was a statistically significant difference for the skin color variable (p<0.05). The prevalences found for sickle cell trait according to skin color was: 4.1% among dark-skinned blacks, 3.6% among light-skinned blacks, 1.2% among whites, and 1.7% among others.
CONCLUSION: The most prevalent hemoglobinopathies were the sickle cell trait and minor thalassemia, and were predominate among light- and dark-skinned black people. The study helps in identifying hemoglobinopathies and in genetic counseling in pre-conception.

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Year:  2019        PMID: 31596378     DOI: 10.1590/1980-549720190007.supl.2

Source DB:  PubMed          Journal:  Rev Bras Epidemiol        ISSN: 1415-790X


  2 in total

1.  Mortality attributed to sickle cell disease in children and adolescents in Brazil, 2000-2019.

Authors:  Maria Isabel do Nascimento; Ana Luísa Ferreira Przibilski; Carolina Sampaio Gomes Coelho; Katyslaine Frossard de Amorim Leite; Mariana Makenze; Stella Bayer de Jesus
Journal:  Rev Saude Publica       Date:  2022-07-01       Impact factor: 2.772

2.  Polymorphisms and avascular necrosis in patients with sickle cell disease - A systematic review.

Authors:  Márcio Passos Leandro; Natália Damasceno Almeida; Lara Santana Hocevar; Cloud Kennedy Couto de Sá; Amâncio José de Souza; Marcos Almeida Matos
Journal:  Rev Paul Pediatr       Date:  2022-05-11
  2 in total

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