Does Obstructive Sleep Apnea Increase Cognitive Deficits in Pediatric Sickle Cell Disease?

Sarah E Bills1, Tal Katz1, Jaleel McNeil1

  • 1Department of Psychology, University of South Carolina, Columbia, South Carolina 29208, USA.

Insights

Children with sickle cell disease (SCD) and obstructive sleep apnea (OSA) show similar cognitive deficits as those with SCD alone. However, severe OSA may worsen neurocognitive impairments in children with SCD.

Area of Science:

  • Pediatric hematology
  • Sleep medicine
  • Neuropsychology

Background:

  • Pediatric obstructive sleep apnea (OSA) affects 2-3% of children, but over 40% of those with sickle cell disease (SCD).
  • Neurocognitive deficits are seen in both pediatric OSA and SCD, yet their interaction is understudied.
  • Understanding this interaction is crucial for managing SCD complications.

Purpose of the Study:

  • To investigate the impact of obstructive sleep apnea (OSA) on neurocognitive deficits in children with sickle cell disease (SCD).
  • To determine if comorbid OSA exacerbates cognitive impairments in children with SCD.

Main Methods:

  • Cognitive function was assessed in three groups: children with SCD and OSA (n=26), children with SCD only (n=39), and healthy children (n=59).
  • Standardized tests measured processing speed, reading decoding, quantitative knowledge, and visual-spatial construction.

Main Results:

  • Children with chronic health conditions (SCD with or without OSA) scored lower on processing speed and reading decoding than healthy children.
  • The SCD-only group performed worse on quantitative knowledge and visual-spatial tests compared to healthy controls.
  • No additive cognitive impact of OSA was found; however, more severe OSA correlated with lower processing speed and quantitative knowledge in the SCD+OSA group.

Conclusions:

  • Comorbid OSA does not worsen cognitive deficits in children with SCD compared to SCD alone.
  • Severe obstructive sleep apnea (OSA) may represent an additional risk factor for neurocognitive impairments in children with sickle cell disease (SCD).
Abstract

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