Brain volume in pediatric patients with sickle cell disease: evidence of volumetric growth delay?

R Grant Steen1, Temitope Emudianughe, Michael Hunte

  • 1Department of Radiological Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA. Grant_Steen@med.unc.edu

Insights

Children with sickle cell disease (SCD) show delayed gray matter brain growth. This finding in pediatric patients suggests potential neurodevelopmental impacts of SCD.

Area of Science:

  • Neurology
  • Pediatrics
  • Radiology

Background:

  • Sickle cell disease (SCD) is known to affect somatic growth.
  • The impact of SCD on brain volumetric growth remains largely uncharacterized.
  • Existing research has not adequately explored neurodevelopmental aspects in pediatric SCD.

Purpose of the Study:

  • To investigate the hypothesis that children with SCD experience delayed brain volumetric growth compared to healthy peers.
  • To assess the specific effects of SCD on different brain tissue volumes.
  • To understand the relationship between SCD and brain development in children.

Main Methods:

  • A cross-sectional study comparing 83 children with SCD and 43 healthy controls.
  • Brain volumes were quantified using segmented MR imaging data (T1, T2, and proton density-weighted images).
  • Linear models analyzed group (patient vs. control) and age effects on brain volumes.

Main Results:

  • No significant difference in total brain volume was observed between SCD patients and controls at 9.5 years.
  • Children with SCD exhibited a significant deficit in gray matter volume (P=.005).
  • Gray matter volume in SCD patients did not change with age, unlike in healthy controls where it decreased, likely due to myelination.

Conclusions:

  • Volumetric growth of gray matter in the brain may be delayed in children with sickle cell disease.
  • These findings suggest potential neurodevelopmental consequences associated with SCD in pediatric populations.
  • Further research is warranted to explore the long-term neurodevelopmental outcomes in children with SCD.
Abstract

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