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Serum resistin levels in children with primary snoring
A M Zicari1, R Cutrera2, F Occasi1
1Department of Pediatrics, Sapienza University of Rome, Italy.
Insights
Children with primary snoring (PS) have higher resistin levels, indicating systemic inflammation. This suggests oxidative stress may contribute to PS pathophysiology, even in normal-weight children.
Area of Science:
- Pediatric Pulmonology
- Endocrinology
- Sleep Medicine
Background:
- Primary snoring (PS) is often underestimated, existing at the milder end of sleep-disordered breathing.
- Children with PS show elevated blood pressure and reduced arterial distensibility.
- Adipokine associations with sleep-disordered breathing (SDB) are increasingly studied, particularly in obstructive sleep apnea (OSA).
Discussion:
- Resistin, an adipokine linked to inflammation and insulin resistance, was investigated in normal-weight children with PS.
- Studies on SDB often focus on OSA, overlooking potential inflammatory pathways in milder conditions like PS.
- This research explores resistin's role in PS, distinct from the more severe, hypoxia-driven inflammation in OSA.
Key Insights:
- Children with primary snoring exhibit significantly higher serum resistin levels compared to healthy controls.
- Elevated resistin levels correlate with inconclusive pulse oximetry readings and increased snoring frequency.
- These findings suggest systemic inflammation and oxidative stress are implicated in the pathophysiology of primary snoring.
Outlook:
- Further research into resistin's specific role in PS pathophysiology is warranted.
- Investigating targeted anti-inflammatory or antioxidant therapies for PS may be beneficial.
- Understanding these mechanisms could lead to earlier detection and intervention for SDB.
Abstract:
Primary Snoring (PS) has been positioned at the milder end of the Sleep-Disordered Breathing severity continuum characterized by snoring and it is usually underestimated. PS is defined as snoring without apnea, frequent arousals, or gas exchange abnormalities and recent studies demonstrated that children with PS have increased blood pressure and reduced arterial distensibility. The association between adipokines and SDB has been recently investigated, though most of the studies were focused on OSAS where intermittent hypoxia characterizing the disease may lead to an inflammatory cascade and to the release of several adipokines, contributing to oxidative stress. Resistin, initially described s an adipokine increasing insulin resistance, has been recently identified as a novel important member of the cytokine family involved in the regulation of inflammation. The aim of our study was to investigate circulating resistin levels in normal weight children with PS. Sixty-five children of normal weight aged between 4 and 14 years of age were selected for habitual snoring. Children with positive polysomnography were excluded from the study. Serum resistin levels were detected in all children with PS. Thirty-three healthy non-snorer children with similar age, sex and BMI were selected as a control group. A significantly higher level of resistin was observed in patients with PS compared to the control group (4.67±1.91 ng/ml vs 3.98±1.58 ng/ml; p<0.01). Patients with inconclusive pulse oximetry showed significantly higher resistin levels than those with negative recordings recordings (5.29±1.91 ng/ml vs 4.20±1.93 ng/ml; p<0.008). Moreover, there was a significant increasing trend between sieric adipokine level and the frequency of snoring (p<0.006). Our results suggest that systemic inflammation and oxidative stress may also play a significant role in the pathophysiology of PS.
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