Neurocognitive and endothelial dysfunction in children with obstructive sleep apnea

David Gozal1, Leila Kheirandish-Gozal, Rakesh Bhattacharjee

  • 1Department of Pediatrics, University of Chicago, 5721 S Maryland Ave, MC 8000, Suite K-160, Chicago, IL 60637, USA. dgozal@uchicago.edu

Pediatrics
|October 20, 2010
PubMed

Insights

Pediatric obstructive sleep apnea syndrome (OSAS) is linked to neurocognitive deficits and endothelial dysfunction. These conditions often coexist in children, suggesting shared underlying causes and the potential for early detection using vascular response tests.

Area of Science:

  • Pediatric Sleep Medicine
  • Neuroscience
  • Cardiovascular Physiology

Background:

  • Pediatric obstructive sleep apnea syndrome (OSAS) is associated with significant neurocognitive and endothelial dysfunction.
  • The relationship and potential shared pathophysiology between these two common OSAS morbidities in children remain unclear.

Purpose of the Study:

  • To concurrently assess neurocognitive deficits and endothelial function in children with OSAS.
  • To investigate whether these morbidities share common pathophysiological mechanisms.

Main Methods:

  • Children aged 5-8 years with polysomnographically confirmed OSAS underwent cognitive testing and cuff-occlusion hyperemic tests for endothelial function assessment.
  • Neurocognitive deficits (NC(+)) were defined by ≥ 2 abnormal cognitive tests; endothelial dysfunction (ED(+)) by a post-hyperemic response time (Tmax) ≥ 45 seconds.

Main Results:

  • In children with OSAS, 48 were NC(+) and 50 had ED(+); over 80% overlapped between these groups.
  • Conversely, only 25.6% of children without neurocognitive deficits had ED(+), and 21.6% without ED(+) had neurocognitive deficits.
  • Approximately one-third of children with OSAS had neither neurocognitive deficits nor endothelial dysfunction, indicating a strong association between the two.

Conclusions:

  • Endothelial dysfunction and neurocognitive deficits frequently coexist in pediatric OSAS, more than expected by chance.
  • These findings suggest shared pathogenetic mechanisms for both morbidities in pediatric OSAS.
  • Post-hyperemic vascular response tests may aid in identifying children at risk for neuropsychological deficits.
Abstract

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