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Treating Sleep Apnea with CPAP Nightly Can Lower Diabetes Risk

Findings suggest that CPAP treatment, if used for 8 hours per night, can help people with prediabetes improve their blood sugar levels and may reduce the risk of progressing to diabetes. …

Many people with prediabetes have untreated sleep apnea, although few of them are aware of it. The most widely accepted treatment for sleep apnea is continuous positive airway pressure (CPAP), a device that blows a constant pressure of air into the lungs through a tube and face mask during the night. This helps people breathe better while they sleep by keeping the upper airway open.

“Our study showed that CPAP in patients with prediabetes can lower their risk of progressing to diabetes when CPAP is used for eight hours, a full night’s sleep,” said the study’s lead author, Sushmita Pamidi, MD, a former fellow at the University of Chicago who is now on the faculty at McGill University in Montreal, Canada. “Although eight hours of CPAP per night can be difficult to achieve in real-life, our results should provide a strong incentive for anyone with sleep apnea, especially prediabetic individuals, to improve adherence to their treatment for cardio-metabolic risk reduction,” she said.

People with sleep apnea, which is common among overweight and obese individuals, have repeated episodes where their upper airway closes during sleep. This can disrupt sleep and temporarily lower oxygen levels. It has been associated with an increased risk of cardiovascular diseases, such as hypertension and stroke, and may decrease their ability to regulate blood sugar levels. This increases the risk of diabetes.

For this study, the researchers recruited 39 middle-aged, overweight or obese volunteers with prediabetes and sleep apnea. Two-thirds of them (26) were randomly assigned to two weeks of CPAP treatment. The other 13 received a placebo to be taken 30 minutes before bedtime. They were told the study would compare the two treatments.

All participants slept in the sleep laboratory and were closely monitored with all-night sleep recordings during the treatment period. Those assigned to CPAP wore the device for eight hours a night under continuous supervision by a technician. Before and after each treatment period, participants’ glucose metabolism was assessed by oral and intravenous glucose-tolerance tests.

The researchers also measured the stress hormone noradrenaline in the blood and continuously monitored blood pressure for 24 hours at home. All participants were permitted to leave the laboratory during the day and engage in their routine activities.

After two weeks, blood sugar control, as measured by an oral glucose tolerance test, improved for those in the CPAP group compared to the oral placebo group. In addition, the ability of insulin to regulate their blood sugar, estimated by the intravenous glucose tolerance test, was improved in the CPAP group compared to the oral placebo group. The CPAP group had, on average, 27 percent lower levels of the stress hormone, norepinephrine, as well as lower blood pressure than the oral placebo group.

“Despite the demonstrated efficacy of lifestyle interventions and the availability of many drug treatments, the economic and public health burden of diabetes remains enormous,” said Esra Tasali, MD, assistant professor of medicine at the University of Chicago and senior author of the study. “Assessment of sleep apnea should be considered in patients at high risk for diabetes and cardiovascular disease, since our study shows that treatment of sleep apnea can reduce these risks.”

 

Practice Pearls:

  • After two weeks of treatment, fasting insulin levels were significantly reduced in the group receiving CPAP compared to the change in the placebo group.
  • Adults with overweight or obesity, prediabetes and sleep apnea who receive overnight continuous positive airway pressure for 8 hours a night may experience improved glucose metabolism and insulin sensitivity.

University of Chicago Medicine News Release

Pamidi S, et al. Published online in the April 21, 2015, issue of the American Journal of Respiratory and Critical Care Medicine. 2015;doi:10.1164/rccm.201408-1564OC.