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T regulatory lymphocytes and endothelial function in pediatric obstructive sleep apnea
Hui-Leng Tan1, David Gozal, Arash Samiei
1Section of Pediatric Sleep Medicine, Department of Pediatrics, Pritzker School of Medicine, Biological Sciences Division, The University of Chicago, Chicago, Illinois, USA.
Insights
Regulatory T cells (Tregs) are linked to endothelial dysfunction in children with obstructive sleep apnea (OSA). Treg function correlates with sleep fragmentation, suggesting a role in cardiovascular risks for pediatric OSA.
Area of Science:
- Immunology
- Pediatrics
- Cardiology
Background:
- Obstructive sleep apnea (OSA) is a chronic inflammatory condition impacting cardiovascular and metabolic health.
- Pediatric OSA is associated with reduced T-regulatory lymphocytes (Tregs), which are crucial for immune regulation.
- Tregs influence endothelial activation and insulin resistance, prompting investigation into their role in pediatric OSA complications.
Purpose of the Study:
- To investigate the association between T-regulatory lymphocytes (Tregs) and endothelial and metabolic dysfunction in children with obstructive sleep apnea (OSA).
- To explore the relationship between Treg percentage, Treg suppressive function, and markers of endothelial function and insulin resistance in pediatric OSA.
Main Methods:
- Fifty children (ages 4.8-12 years) with OSA underwent polysomnography and assessment of insulin resistance via HOMA.
- Flow cytometry was used to determine the percentage of circulating Tregs.
- Endothelial function was assessed by measuring the time to peak occlusive hyperemia (Tmax); in vitro Treg suppression tests were performed in a subgroup.
Main Results:
- Circulating Tregs showed no significant association with BMI z-score or HOMA (insulin resistance).
- A significant inverse correlation was found between Treg percentage and Tmax, indicating impaired endothelial function (p<0.0001, r=-0.56).
- Treg suppressive function negatively correlated with the sleep pressure score (SPS), a marker of sleep fragmentation (p=0.02, r=-0.51).
Conclusions:
- Endothelial dysfunction in pediatric OSA is significantly associated with circulating Tregs and their suppressive capacity.
- The findings suggest that Treg alterations, potentially linked to sleep fragmentation, may contribute to cardiovascular morbidity in children with OSA.
- Insulin resistance was not found to be associated with Treg levels in this pediatric OSA cohort.
Background:
Obstructive sleep apnea (OSA) is a low-grade inflammatory disease affecting the cardiovascular and metabolic systems. Increasing OSA severity reduces T-regulatory lymphocytes (Tregs) in OSA children. Since Tregs modulate endothelial activation, and attenuate insulin resistance, we hypothesized that Tregs are associated with endothelial and metabolic dysfunction in pediatric OSA.
Methods:
50 consecutively recruited children (ages 4.8-12 years) underwent overnight polysomnography and fasting homeostatic model (HOMA) of insulin resistance was assessed. Percentage of Tregs using flow cytometry, and endothelial function, expressed as the time to peak occlusive hyperemia (Tmax), were examined. In a subgroup of children (n = 21), in vitro Treg suppression tests were performed.
Results:
Circulating Tregs were not significantly associated with either BMI z score or HOMA. However, a significant inverse correlation between percentage of Tregs and Tmax emerged (p<0.0001, r = -0.56). A significant negative correlation between Tregs suppression and the sleep pressure score (SPS), a surrogate measure of sleep fragmentation emerged (p = 0.02, r = -0.51) emerged, but was not present with AHI.
Conclusions:
Endothelial function, but not insulin resistance, in OSA children is strongly associated with circulating Tregs and their suppressive function, and appears to correlate with sleep fragmentation. Thus, alterations in T cell lymphocytes may contribute to cardiovascular morbidity in pediatric OSA.
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