Epidemiologic profile of hemoglobinopathies in Benin

Selma Gomez1, Adjile Edjide Roukiyath Amoussa2, Edwige Dedjinou3

  • 1Centre de Prise en charge Médicale Intégrée du Nourrisson et de la Femme Enceinte atteints de Drépanocytose (CPMI-NFED), Benin; Laboratory of Biology and Molecular Typing in Microbiology, University of Abomey-Calavi, Benin.

Insights

Sickle cell disease screening is crucial in Benin, revealing a high prevalence of hemoglobinopathies. Early detection through newborn screening and genetic counseling is vital for prevention.

Area of Science:

  • Hematology
  • Genetics
  • Public Health

Background:

  • Sickle cell disease is a major global inherited blood disorder, prioritized by the WHO in Africa.
  • Prevention strategies include newborn screening and genetic counseling for at-risk couples.
  • Understanding local prevalence is key to effective public health interventions.

Purpose of the Study:

  • To investigate the epidemiological profile of sickle cell disease and hemoglobinopathies in Benin.
  • To determine current prevalence rates of these conditions in the population.

Main Methods:

  • Quantitative electrophoresis was used to analyze hemoglobin profiles of 2910 participants.
  • Complete blood counts were performed on samples with abnormal hemoglobin results.

Main Results:

  • The study included 1528 males and 1382 females, with a mean age of 26 years.
  • Prevalence included Hb AS (21.7%), Hb AC (10.2%), Hb SS (3.1%), Hb SC (3.7%), and rare phenotypes (1.6%).
  • Abnormal hemoglobin carriers presented with normochromic normocytic anemia; only 12% knew their status.

Conclusions:

  • The study underscores the significant prevalence of hemoglobinopathies in Benin.
  • Highlights the critical need for widespread population screening programs.
  • Emphasizes the importance of early detection for disease management and prevention.
Abstract

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