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1.
Eur Respir J ; 46(3): 717-27, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26065566

ABSTRACT

The first line of treatment of obstructive sleep apnoea syndrome (OSAS) in children consists of adenotonsillectomy (T&A). The aim of the present study was to evaluate treatment outcomes of OSAS among obese children recruited from the community.A cross-sectional, prospective, multicentre study of Spanish obese children aged 3-14 years, with four groups available for follow-up: group 1: non-OSAS with no treatment; group 2: dietary treatment; group 3: surgical treatment; and group 4: continuous positive airway pressure treatment.117 obese children (60 boys, 57 girls) with a mean age of 11.3±2.9 years completed the initial (T0) and follow-up (T1) assessments. Their mean body mass index (BMI) at T1 was 27.6±4.7 kg·m(-2), corresponding to a BMI Z-score of 1.34±0.59. Mean respiratory disturbance index (RDI) at follow-up was 3.3±3.9 events·h(-1). Among group 1 children, 21.2% had an RDI ≥3 events·h(-1) at T1, the latter being present in 50% of group 2, and 43.5% in group 3. In the binary logistic regression model, age emerged as a significant risk factor for residual OSAS (odds ratio 1.49, 95% confidence interval 1.01-2.23; p<0.05) in obese children surgically treated, and RDI at T0 as well as an increase in BMI emerged as significant risk factors for persistent OSAS in obese children with dietary treatment (OR 1.82, 95% CI 1.09-3.02 (p<0.03) and OR 8.71, 95% CI 1.24-61.17 (p=0.03)).Age, RDI at diagnosis and obesity are risk factors for relatively unfavourable OSAS treatment outcomes at follow-up.


Subject(s)
Body Mass Index , Obesity/complications , Sleep Apnea, Obstructive/complications , Sleep Apnea, Obstructive/therapy , Adenoidectomy/methods , Adolescent , Child , Child, Preschool , Continuous Positive Airway Pressure/methods , Cross-Sectional Studies , Female , Follow-Up Studies , Humans , Linear Models , Logistic Models , Male , Obesity/diagnosis , Obesity/diet therapy , Polysomnography/methods , Prospective Studies , Risk Assessment , Severity of Illness Index , Sleep Apnea, Obstructive/diagnosis , Spain , Tonsillectomy/methods , Treatment Outcome
2.
Mediators Inflamm ; 2014: 605280, 2014.
Article in English | MEDLINE | ID: mdl-24991089

ABSTRACT

INTRODUCTION: Obesity and obstructive sleep apnea syndrome (OSA) are common coexisting conditions associated with a chronic low-grade inflammatory state underlying some of the cognitive, metabolic, and cardiovascular morbidities. AIM: To examine the levels of inflammatory markers in obese community-dwelling children with OSA, as compared to no-OSA, and their association with clinical and polysomnographic (PSG) variables. Methods. In this cross-sectional, prospective multicenter study, healthy obese Spanish children (ages 4-15 years) were randomly selected and underwent nocturnal PSG followed by a morning fasting blood draw. Plasma samples were assayed for multiple inflammatory markers. RESULTS: 204 children were enrolled in the study; 75 had OSA, defined by an obstructive respiratory disturbance index (RDI) of 3 events/hour total sleep time (TST). BMI, gender, and age were similar in OSA and no-OSA children. Monocyte chemoattractant protein-1 (MCP-1) and plasminogen activator inhibitor-1 (PAI-1) levels were significantly higher in OSA children, with interleukin-6 concentrations being higher in moderate-severe OSA (i.e., AHI > 5/hrTST; P < 0.01), while MCP-1 levels were associated with more prolonged nocturnal hypercapnia (P < 0.001). CONCLUSION: IL-6, MCP-1, and PAI-1 are altered in the context of OSA among community-based obese children further reinforcing the proinflammatory effects of sleep disorders such as OSA. This trial is registered with ClinicalTrials.gov NCT01322763.


Subject(s)
Obesity/blood , Obesity/physiopathology , Sleep Apnea, Obstructive/blood , Sleep Apnea, Obstructive/physiopathology , Adolescent , Animals , Chemokine CCL2/blood , Child , Child, Preschool , Cross-Sectional Studies , Female , Humans , Interleukin-6/blood , Male , Plasminogen Activator Inhibitor 1/blood , Prospective Studies
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