Screening for Iron Deficiency Anemia in Infants in a Thalassemia-endemic Region

Natthawadee Nanta1, Rungrote Natesirinilkul1, Kulnipa Kittisakmontri1

  • 1Department of Pediatrics, Faculty of Medicine, Chiang Mai University.

Insights

Screening infants for iron deficiency anemia (IDA) and thalassemia carriers requires careful evaluation. The Mentzer index, alongside hemoglobin levels, effectively aids in distinguishing these conditions in endemic areas.

Area of Science:

  • Pediatric Hematology
  • Nutritional Anemias
  • Genetic Blood Disorders

Background:

  • Iron deficiency anemia (IDA) screening in infants typically relies on hemoglobin (Hb) and mean corpuscular volume (MCV).
  • Co inherited thalassemia carrier status can complicate IDA diagnosis in infants.
  • Thalassemia is prevalent in many regions, necessitating accurate diagnostic approaches.

Purpose of the Study:

  • To differentiate hematologic parameters in infants with IDA versus thalassemia carriers.
  • To evaluate the utility of red blood cell indices for IDA screening in a thalassemia-endemic setting.
  • To identify reliable markers for simultaneous screening of IDA and thalassemia carriers in infants.

Main Methods:

  • Enrollment of healthy infants aged 6-12 months for hematologic analysis.
  • Collection of blood for complete blood count, ferritin, Hb analysis, and alpha-thalassemia genotyping.
  • Calculation and analysis of red cell parameters, including the Mentzer index, to distinguish thalassemia carriers.

Main Results:

  • Of 85 infants, 18.8% had IDA and 29.4% were thalassemia carriers.
  • Both IDA and thalassemia carrier groups exhibited significantly lower Hb levels and MCV compared to controls.
  • The Mentzer index demonstrated high diagnostic performance (AUC 0.867) for identifying thalassemia carriers.

Conclusions:

  • Hemoglobin level and Mentzer index are valuable tools for screening IDA in infants.
  • Combined screening using Hb and Mentzer index can effectively identify both IDA and thalassemia carriers.
  • These parameters are recommended for population-based screening in thalassemia-endemic areas.