Sibling risk of pediatric obstructive sleep apnea syndrome and adenotonsillar hypertrophy

Danielle Friberg1, Jan Sundquist, Xinjun Li

  • 1Department of Otorhinolaryngology, Karolinska Institutet, Stockholm, Sweden. danielle.friberg@karolinska.se

Sleep
|September 4, 2009
PubMed

Insights

Children with sleep disordered breathing (SDB) have a significantly increased risk if a sibling also has SDB. This suggests genetic or environmental factors contribute to the condition, warranting early screening for siblings.

Area of Science:

  • Pediatrics
  • Genetics
  • Public Health

Background:

  • Sleep disordered breathing (SDB) is a common condition in children.
  • Obstructive sleep apnea syndrome (OSAS) and adenotonsillar hypertrophy are key diagnoses within SDB.

Purpose of the Study:

  • To determine the sibling risk for childhood SDB, specifically OSAS and adenotonsillar hypertrophy.
  • To analyze this risk within the total Swedish population.

Main Methods:

  • Utilized the MigMed database for individuals aged 0-18 years in Sweden (1978-2004).
  • Identified sibling groups and calculated standardized incidence ratios (SIRs) for affected individuals compared to unaffected siblings.
  • Controlled for socioeconomic status, age, and geographic region.

Main Results:

  • Boys with a sibling diagnosed with OSAS had a 33.2-fold increased risk; girls had a 40.5-fold increased risk.
  • For adenotonsillar hypertrophy, sibling SIRs were 4.53 for boys and 4.94 for girls.
  • These findings indicate a substantial familial aggregation of SDB.

Conclusions:

  • A significant increased sibling risk for SDB exists in children.
  • This risk may stem from genetic predispositions or shared environmental factors.
  • Healthcare providers should inquire about sibling symptoms for early SDB detection and intervention.
Abstract

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