Effects of sleep-disordered breathing on serum lipid levels in children:a case control study

Lei Lei1, XiaoYun Zhang1, Binbin Wang1

  • 1Department of Otorhinolaryngology, Head&Neck Surgery, West China Hospital, West China Medical School, Sichuan University, Sichuan, China.

BMC Pediatrics
|April 2, 2024
PubMed

Insights

Childhood sleep-disordered breathing (SDB) significantly impacts blood lipids. Even primary snoring (PS) elevates lipid levels, contrary to previous beliefs, with obesity affecting triglyceride levels.

Area of Science:

  • Pediatric Pulmonology
  • Sleep Medicine
  • Clinical Biochemistry

Background:

  • Childhood sleep-disordered breathing (SDB) encompasses primary snoring (PS) and obstructive sleep apnea syndrome (OSAS).
  • While OSAS is linked to health issues, PS was considered less harmful.
  • Emerging evidence suggests PS may also contribute to cardiovascular, cognitive, and behavioral problems.

Purpose of the Study:

  • To investigate the association between serum lipid profiles and SDB components in children.
  • To compare lipid levels in children with OSAS, PS, and healthy controls.
  • To explore the role of obesity in SDB and lipid metabolism.

Main Methods:

  • Cross-sectional study involving children with habitual snoring or mouth breathing (SDB group) and matched controls.
  • Polysomnography was performed on SDB group participants.
  • Serum lipid profiles (TC, TG, HDL-C, LDL-C) were measured using enzymatic assays.

Main Results:

  • Children with OSAS showed significantly higher TC, TG, LDL-C, and LDL/HDL ratios compared to PS and control groups.
  • The PS group also exhibited higher lipid levels than the control group.
  • Serum triglycerides correlated negatively with lowest oxygen saturation and positively with BMI-z score; obese children had higher TG levels.

Conclusions:

  • SDB significantly affects blood lipid profiles in children, even in cases of PS without significant apnea or hypoxia.
  • Obesity is specifically associated with elevated triglyceride levels in children with SDB.
Abstract

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