Obesity Clinical Trial
Official title:
Does Treating Obstructive Sleep Apnea in Obese Canadian Youth Improve Blood Sugar Control? A Multi-Centered Prospective Cohort Study
To determine whether, in obese children with moderate-severe Obstructive Sleep Apnea who are prescribed Positive Airway Pressure(PAP) therapy, increased hours of PAP usage per night over a one-year period is associated with a greater improvement in HOMA-IR
Rationale: The five-fold increase in prevalence of childhood obesity in Canada over the last
15 years has led to an increasing number of pediatric cases of obesity-related obstructive
sleep apnea (OSA). Not only is the prevalence of OSA significantly higher among obese
children compared with the general population, but in this group, routine treatment by
adenotonsillectomy has a much lower cure rate. Instead, Positive Airway Pressure (PAP)
treatment is usually prescribed. Other complications of obesity are also increasingly
recognized in children, including metabolic disturbances with insulin resistance (IR). This
is particularly concerning, since IR is an identified surrogate measure of future
obesity-related sequelae, such as diabetes, dyslipidemia, cardiovascular disease (including
hypertension, and heart rate disturbances), inflammation and impaired quality of life. Of
particular interest, the IR related to obesity can be exacerbated by OSA and the severity of
IR correlates with the severity of OSA. IR is measured using a homeostasis model assessment
of insulin resistance (HOMA-IR) and is calculated from fasting blood glucose and insulin
levels. In obese adults with OSA, HOMA-IR, as well as cardiovascular and other metabolic
markers, has been shown to improve following PAP therapy. Such a study has not been done in
children. We hypothesize that PAP treatment for obese children with moderate-severe OSA will
improve markers of obesity-related disease.
Primary Objective: To determine whether, in obese children with moderate-severe OSA who are
prescribed PAP therapy, increased hours of PAP usage per night over a one-year period is
associated with a greater improvement in HOMA-IR. Secondary Objectives: To determine whether
increased hours of PAP usage per night is associated with a greater improvement in the
following outcomes: 1) sympathetic nervous system activation (systolic and diastolic
hypertension, nocturnal hypertension, heart rate and heart rate variability); 2) inflammation
3) neurobehavioral and quality of life measures. Methods: Study design: prospective
multi-centre cohort study. Study Population: Obese children (body mass index (BMI) ≥ 95th
%ile for age and sex) 8-17 years old with moderate-severe OSA will be recruited for this
study from four pediatric tertiary care centres across Canada. As per current standard of
care, those children with moderate-severe OSA, defined as ≥ 10 obstructive events per hour on
polysomnography, will be prescribed PAP treatment. Sample Size: We expect a medium effect
size (0.5); therefore 10 subjects per parameter tested (n=4) in the regression model and 25%
attrition requires the recruitment of 54 subjects. Measurements will be made at baseline and
12 months. Data collection will include HOMA-IR, 24-hr blood pressure measurements,
electrocardiogram for heart rate and heart rate variability, C-reactive protein as a marker
of inflammation, neurobehavioral/quality of life measures (Conners parent and teacher scales,
Child Behavior Checklist and Pediatric Quality of Life Inventory) and physical activity
questionnaire (Habitual Activity Estimation Scale (HAES)). Data Analysis: Multivariate linear
regression analyses will be performed for our primary and secondary outcomes. Our dependent
variable will be change in HOMA-IR; our primary independent variable will be average number
of hours/night of PAP usage. Adjustment variables will be change in BMI %ile, pubertal stage
(Tanner stage 1-2 vs.
3-5), and change in HAES. Similar analyses will be performed for our secondary outcomes.
Importance: Treatment of obesity-related OSA in adults has been shown to reduce morbidity and
mortality. Our study is uniquely poised and timely, as it will be the first to examine the
impact of PAP therapy in children on measures of insulin resistance and other obesity-related
conditions. It will raise awareness of co-morbidities of obesity and OSA in childhood and
support early intervention, before irreversible end-organ damage has occurred.
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