The purpose of this study is to determine if the treatment of Obstructive sleep apnea (OSA) by hypoglossal nerve stimulation (HGNS) will alter glucose metabolism. The study team will also determine if the treatment of Obstructive sleep apnea (OSA) by (hypoglossal nerve stimulation) HGNS will alter predictors of cardiovascular outcomes.
Obstructive sleep apnea (OSA) is a highly prevalent sleep disorder in the general population. It is estimated that 80 percent of those who have OSA remain undiagnosed, and thus do not receive therapy. Strong evidence from epidemiologic and clinical studies suggests that untreated OSA is an independent risk factor for cardiometabolic disease, particularly among those with moderate-to-severe OSA. Animal and human models have revealed that intermittent hypoxia and sleep fragmentation (i.e., main features of OSA) result in insulin resistance, glucose intolerance and pancreatic beta-cell dysfunction, hypertension and dyslipidemia. Continuous positive airway pressure (CPAP) is the established first-line treatment for OSA. However, only 50% of patients with OSA are adherent to CPAP therapy. Notably, a key limitation of prior CPAP trials on cardiometabolic outcomes is low treatment adherence. A randomized controlled trial conducted at the University of Chicago demonstrated that 8 hours of nightly CPAP reduces glucose response during oral glucose tolerance testing and improves insulin sensitivity in individuals with OSA and prediabetes. In 2014, following the pivotal Safe and Timely Antithrombotic Removal - Ticagrelor trial (STAR), the Food and Drug Administration (FDA) approved hypoglossal nerve stimulation (HNS) as an alternative therapy for OSA. Five-year outcomes from STAR have confirmed durable efficacy, tolerance, and safety for HNS. From improved tolerance and adherence, it is theorized that HNS may be more effective than CPAP at ameliorating cardiovascular and diabetes risk. Yet, there is no literature on the cardiometabolic outcomes of treating OSA with HNS. The study team's long-term goal is to understand the metabolic and cardiovascular effects of OSA and how current therapies can mitigate risk and improve outcomes. The overall objective of this study is to determine the cardiometabolic impact of HNS therapy in patients with moderate-to-severe OSA who are intolerant to CPAP. It is hypothesized by the investigator that effective HNS treatment will improve glucose metabolism and markers of cardiovascular disease.
Study Type
OBSERVATIONAL
Enrollment
30
Alternative therapy for Obstructive Sleep Apnea
The University of Chicago
Chicago, Illinois, United States
RECRUITINGGlycemic variability
measured by standard deviation (SD) of average blood glucose or % coefficient of variation (SD / mean glucose) on two-week continuous glucose monitor
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-op
Mean systolic BP (daytime and nocturnal)
important mediators of cardiovascular outcomes
Time frame: 24 hrs at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-op
Glycemic variability
measured by standard deviation (SD) of % coefficient of variation (SD / mean glucose) on two-week continuous glucose monitor
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-op
mean blood glucose levels
other glycemic metrics for the clinical care of diabetes to be followed.
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op
mean ambulatory glucose excursions
glycemic metrics for the clinical care of diabetes will be followed
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op
time blocks
glycemic metrics for the clinical care of diabetes will be followed
Time frame: 24-h, day, night at baseline and after HGNS implant, acclimation, and tuning
Morning fasting insulin, including calculated insulin resistance (HOMA-IR)
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op
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Mean norepinephrine levels
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op
Morning fasting blood glucose
markers of glucose metabolism
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op
Hemoglobin A1c
markers of glucose metabolism
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op
Insulin levels
markers of glucose metabolism
Time frame: at baseline and after HGNS implant, acclimation, and tuning
c-peptide levels
markers of glucose metabolism
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op
fasting lipid profile (triglycerides)
testing for signs of cardiovascular disease
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op
heart rate indices by activity monitor
testing for signs of cardiovascular disease
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op
sympathetic activity by plasma norepinephrine
to investigate its role as a mediator in cardiometabolic response to treatment
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op
Morning fasting insulin of c-peptide level
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op
fasting lipid profile (HDL- cholesterol)
testing for signs of cardiovascular disease
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op
fasting lipid profile ( LDL-cholesterol)
testing for signs of cardiovascular disease
Time frame: at baseline and after HGNS implant, acclimation, and tuning at 3 month Post-Op