Sleep disordered breathing is associated with impaired glucose tolerance and incident diabetes. Nocturnal hypoxemia is a potential stimulus of glucose intolerance. It is especially severe and highly prevalent in high altitude residents. Intervening on nocturnal hypoxemia may therefore improve glucose control and decrease the public health burden in high altitude populations. The objective of this study is to examine the impact of hypoxemia on glucose homeostasis in high altitude residents. The investigators will address this objective by examining the effect of supplemental oxygen on glucose in a randomized cross-over study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Participants will be instructed to use compressed air during sleep as a placebo control.
Participants will be instructed to use supplemental oxygen at rate of 2lpm during sleep.
Mean glucose level
average glucose (mg/dL) during sleep assessed via continuous glucose monitoring
Time frame: 14 days after start of intervention
Mean fasting glucose level
Mean fasting glucose level (mg/dL)
Time frame: 14 days after start of intervention
Mean fasting insulin
Fasting insulin (U/mL)
Time frame: 14 days after start of intervention
Morning blood pressure
Morning blood pressure (mmHg)
Time frame: 14 days after start of intervention
Inflammatory marker interleukin-6 (IL-6)
Inflammatory marker interleukin-6 (IL-6) (pg/mL) level in plasma assessed by electrochemiluminescence as a measure of systemic inflammation
Time frame: 14 days after start of intervention
Tumor Necrosis Factor alpha (TNF-a) level in blood (picogram/milliliter)
Tumor Necrosis Factor alpha level in blood as a marker of inflammation
Time frame: 14 days after start of intervention
C-Reactive Protein (CRP) level in blood (mg/L)
C-Reactive Protein (CRP) level in blood as a marker of inflammation
Time frame: 14 days after start of intervention
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