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Author Spotlight: Assessing the Cardiovascular Profile of Patients with Metabolic Syndrome
Published on: September 27, 2024
Cardiometabolic risk profile in non-obese children with obstructive sleep apnea syndrome
Anna Di Sessa1, Giovanni Messina2, Ilaria Bitetti3
1Department of Woman, Child, and General and Specialized Surgery, University of Campania "Luigi Vanvitelli", Naples, Italy. anna.disessa@unicampania.it.
Insights
Childhood obstructive sleep apnea syndrome (OSAS) is linked to inflammation and cardiometabolic risks, even in non-obese children. Early OSAS treatment may improve long-term health outcomes and quality of life.
Area of Science:
- Pediatric Pulmonology
- Pediatric Cardiology
- Pediatric Endocrinology
Background:
- Childhood obstructive sleep apnea syndrome (OSAS) is strongly associated with obesity and its cardiometabolic complications.
- Inflammation is a key shared pathogenic factor in both obesity and OSAS.
Purpose of the Study:
- To investigate the cardiometabolic risk profile in non-obese children diagnosed with OSAS.
- To explore the association between inflammation markers and OSAS in this pediatric population.
Main Methods:
- A cohort of 128 school-aged children with OSAS and 213 healthy controls were assessed.
- Comprehensive clinical and biochemical evaluations included inflammatory markers (WBC, PLT, MPV, NEU%, CRP, ESR, ferritin) and metabolic parameters (glucose, transaminases, uric acid, insulin).
Main Results:
- Children with OSAS exhibited significantly elevated inflammation markers (WBC, PLT, MPV, NEU%, ferritin, CRP, ESR) compared to controls (p < 0.001).
- OSAS patients also showed increased levels of transaminases, glucose, uric acid, and insulin (p < 0.001).
Conclusions:
- Non-obese children with OSAS present with a significantly worse cardiometabolic risk profile.
- Targeting inflammation in OSAS treatment may mitigate cardiometabolic risks and enhance long-term quality of life.
Abstract:
Obstructive sleep apnea syndrome (OSAS) in childhood is a complex disease primarily due both to adenotonsillar hypertrophy and pediatric obesity. Notably, inflammation has been recognized as one of the most important shared pathogenic factor between obesity and OSAS resulting in an increased cardiometabolic risk for these patients. To date, evidence is still limited in non-obese population with OSAS. We aimed to evaluate the cardiometabolic risk profile of a pediatric population of non-obese subjects affected by OSAS. A total of 128 school-aged children (mean age 9.70 ± 3.43) diagnosed with OSAS and 213 non-OSAS children (mean age 9.52 ± 3.35) as control group were enrolled. All subjects underwent a complete clinical and biochemical assessment (including white blood cell count (WBC), platelet count (PLT), mean platelet volume (MPV), % of neutrophils (NEU%), C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), serum glucose, aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma-glutamyl transpeptidase (GGT), uric acid, fasting insulin, iron, ferritin, and transferrin levels). A significant association between inflammation markers (including WBC, PLT, MPV, NEU%, ferritin, CPR, and ESR) and OSAS was found (all p < 0.001). Children with OSAS also showed increased transaminase, glucose, uric acid, and insulin levels (all p < 0.001) compared to healthy controls.
Conclusion:
Taken together, these findings suggested a worse cardiometabolic profile in non-obese children with OSAS. Given the pivotal pathogenic role of inflammation both for hypoxiemia and metabolic derangements, therapeutic strategies for OSAS might also counteract the increased cardiometabolic risk of these patients, by improving their long-term quality of life.
What Is Known:
• Pediatric OSAS has shown a close relationship with obesity and its cardiometabolic comorbidities. • Inflammation represents the hallmark of both obesity and OSAS.
What Is New:
• Non obese children with OSAS presented with a worse cardiometabolic risk profile. • OSAS treatment might serve as an effective approach also for the increased cardiometabolic risk of these children.
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