Fava Bean- Versus Non-Fava Bean-Induced Acute Hemolytic Crisis in Children With Glucose-6-Phosphate Dehydrogenase

Gowda Parameshwara Prashanth1, Mohammed Al-Shafey2, Anita Tandon3

  • 1National University of Science & Technology, College of Medicine and Health Sciences, Sohar, Oman.

Pediatric Blood & Cancer
|February 16, 2025
PubMed

Insights

Children with Glucose-6-phosphate dehydrogenase (G6PD) deficiency experiencing fava bean-induced hemolysis (FBIH) show more severe acute hemolytic episodes (AHEs) than those with non-fava bean-induced hemolysis (NFBIH). Early risk stratification is possible using clinical and lab markers.

Area of Science:

  • Hematology
  • Genetics
  • Pediatrics

Background:

  • Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common red cell enzymopathy.
  • Oxidative stressors, including fava beans, can trigger acute hemolytic episodes (AHEs) in individuals with G6PD deficiency.

Purpose of the Study:

  • To compare the clinical characteristics of fava bean-induced hemolysis (FBIH) with non-fava bean-induced hemolysis (NFBIH) in children with G6PD deficiency.
  • To identify predictors for severity in AHEs within a high-prevalence setting.

Main Methods:

  • A prospective cohort study analyzed hospital records of children hospitalized for AHE due to G6PD deficiency over three years.
  • Participants were classified into FBIH and NFBIH groups based on the precipitating factor.

Main Results:

  • Fava bean-induced hemolysis (FBIH) accounted for 51.6% of AHEs.
  • Children with FBIH were younger, presented more frequently with abdominal pain, and exhibited greater hemolysis severity (lower hemoglobin levels).
  • Elevated levels of serum ferritin, blood urea, lactate dehydrogenase, and alkaline phosphatase were observed in the FBIH group.

Conclusions:

  • Children with FBIH experience more severe hemolytic episodes than those with NFBIH.
  • Clinical and laboratory parameters can aid in early risk stratification for AHEs.
  • Culturally sensitive dietary education is crucial, and further research into G6PD genotypes is warranted.
Abstract