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Effects of adenotonsillectomy on plasma inflammatory biomarkers in obese children with obstructive sleep apnea: A
L Kheirandish-Gozal1, A Gileles-Hillel1, M L Alonso-Álvarez2
1Section of Sleep Medicine, Department of Pediatrics, Pritzker School of Medicine, Biological Sciences Division, The University of Chicago, Chicago, IL, USA.
Insights
Adenotonsillectomy (T&A) reduced key inflammatory markers in obese children with obstructive sleep apnea syndrome (OSA). This suggests T&A can reverse OSA-related inflammation, potentially mitigating associated health risks.
Area of Science:
- Pediatric Endocrinology
- Sleep Medicine
- Immunology
Background:
- Obesity and obstructive sleep apnea syndrome (OSA) frequently coexist in children.
- This overlap is linked to systemic inflammation, contributing to end-organ damage.
Purpose of the Study:
- To investigate the impact of adenotonsillectomy (T&A) on inflammatory markers in obese children diagnosed with OSA.
- To assess changes in plasma biomarkers following T&A in this pediatric population.
Main Methods:
- Prospective study of obese children with polysomnographically diagnosed OSA undergoing T&A.
- Collection of plasma samples pre- and post-T&A for analysis of inflammatory and metabolic markers.
- Evaluation of polysomnography (PSG) results before and after T&A.
Main Results:
- One-third of children showed normalized PSG after T&A (AHI ≤1/hour).
- Significant decreases observed in MCP-1, PAI-1, MMP-9, IL-18, and IL-6 post-T&A.
- Increases noted in adropin and osteocrin plasma levels after T&A.
Conclusions:
- Obstructive sleep apnea syndrome in obese children is associated with reversible alterations in systemic inflammatory and metabolic biomarkers.
- These findings support the pro-inflammatory interplay between OSA and obesity, impacting long-term health.
- T&A may offer a therapeutic strategy to modulate these biomarkers and reduce associated morbidities.
Background:
Obesity and obstructive sleep apnea syndrome (OSA) are highly prevalent and frequently overlapping conditions in children that lead to systemic inflammation, the latter being implicated in the various end-organ morbidities associated with these conditions.
Aim:
To examine the effects of adenotonsillectomy (T&A) on plasma levels of inflammatory markers in obese children with polysomnographically diagnosed OSA who were prospectively recruited from the community.
Methods:
Obese children prospectively diagnosed with OSA, underwent T&A and a second overnight polysomnogram (PSG) after surgery. Plasma fasting morning samples obtained after each of the two PSGs were assayed for multiple inflammatory and metabolic markers including interleukin (IL)-6, IL-18, plasminogen activator inhibitor-1 (PAI-1), monocyte chemoattractant protein-1 (MCP-1), matrix metalloproteinase-9 (MMP-9), adiponectin, apelin C, leptin and osteocrin.
Results:
Out of 122 potential candidates, 100 obese children with OSA completed the study with only one-third exhibiting normalization of their PSG after T&A (that is, apnea-hypopnea index (AHI) ≤1/hour total sleep time). However, overall significant decreases in MCP-1, PAI-1, MMP-9, IL-18 and IL-6, and increases in adropin and osteocrin plasma concentrations occurred after T&A. Several of the T&A-responsive biomarkers exhibited excellent sensitivity and moderate specificity to predict residual OSA (that is, AHI⩾5/hTST).
Conclusions:
A defined subset of systemic inflammatory and metabolic biomarkers is reversibly altered in the context of OSA among community-based obese children, further reinforcing the concept on the interactive pro-inflammatory effects of sleep disorders such as OSA and obesity contributing to downstream end-organ morbidities.
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