Prevalence of Duffy null and its impact on hydroxyurea in young children with sickle cell disease in the United States

Fathia Oladipupo, Joseph Stanek, Joseph Walden, Jennifer Young, Melissa J. Rose, Kathleen Nicol, Anthony Villella, Susan Creary

Research output: Contribution to journalArticlepeer-review

Abstract

Consistent with studies showing a high prevalence of the Duffy null phenotype among healthy Black Americans, this retrospective study found that Duffy null was present in >75% of a young and contemporary cohort of children with sickle cell disease (SCD) in the United States. Despite the potential for this phenotype to impact absolute neutrophil counts, hydroxyurea (HU) dosing, and outcomes, it was not associated with being prescribed a lower HU dose or having increased acute SCD visits early in the HU treatment course. Future studies are needed to confirm these findings in older children with SCD.

Original languageEnglish
Article numbere30945
JournalPediatric Blood and Cancer
Volume71
Issue number6
DOIs
StateAccepted/In press - 2024

Keywords

  • hydroxyurea
  • outcomes research
  • sickle cell anemia
  • sickle cell disease

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