For every unit of BMI increase over 32, the odds of successful treatment decrease by about 17%, a new study finds.

Summary: A nerve-stimulation therapy for obstructive sleep apnea, first approved for patients within a healthy BMI range, was extended to include those with BMIs up to 40. However, a Washington University School of Medicine study finds the treatment’s effectiveness decreases significantly with higher BMIs. Analysis of 76 patients showed a 75% lower success rate in those with BMIs of 32 to 35. This finding underscores the importance of considering weight in evaluating treatment options for sleep apnea.

Key Takeaways:

  • The eligibility for hypoglossal nerve stimulation treatment for obstructive sleep apnea includes patients with BMIs up to 40.
  • Research from Washington University School of Medicine suggests the likelihood of successful treatment decreases as a patient’s BMI increases, with a particularly noted drop in efficacy for patients with BMIs of 32 to 35.
  • The Inspire device, the only FDA-approved hypoglossal nerve-stimulation device for sleep apnea, has been implanted in about 50,000 patients worldwide.

A nerve-stimulation treatment for obstructive sleep apnea that originally was approved only for people with body mass indexes (BMIs) in the healthy range recently was extended to patients with BMIs up to 40, a weight range generally described as severely obese. A healthy BMI ranges from 18.5 to 24.9.

The expanded eligibility criteria for the treatment provide more sleep apnea patients with access to the increasingly popular therapy, known as hypoglossal nerve stimulation. However, new research from Washington University School of Medicine indicates that the likelihood of successful nerve-stimulation treatment drops significantly as a patient’s weight rises above a healthy range.

The study, which appears JAMA Otolaryngology-Head & Neck Surgery, is based on a retrospective analysis of treatment success in 76 sleep apnea patients with BMIs of less than 35.

“Our study shows that the more overweight you are, the less likely it is that nerve-stimulation treatment will be effective in treating your sleep apnea,” says senior author Eric C. Landsness, MD, PhD, an assistant professor of neurology, in a release. “I’m not saying that we shouldn’t put this device in patients with a BMI of 38 or 40. But my job as a physician is to help overweight patients make an informed decision, to better understand their odds of success and realize that the chances of it working for them may be a lot less.”

An Appealing Alternative to CPAP

Sleep apnea most often is treated with a continuous positive airway pressure (CPAP) machine. CPAP machines are effective, but they can be loud and uncomfortable and are largely unpopular. About half of those who try the approach fail to stick with it, according to a release from Washington University School of Medicine.

To many patients, hypoglossal nerve stimulation looks like an appealing alternative to CPAP machines. The therapy is driven by a small, battery-operated device implanted just above the ribs. A small wire is run internally up the chest and into the jaw, where it connects to the hypoglossal, a nerve that controls tongue muscles responsible for keeping the upper airway open during sleep.

Each time the patient takes a breath, the device delivers electrical impulses to the hypoglossal nerve, causing the tongue to move forward just far enough to avoid the airway blockages that drive sleep apnea.

Expanding BMI

The first hypoglossal nerve-stimulation device (brand name Inspire) was approved by the US Food and Drug Administration (FDA) in 2014 for use in patients with BMIs less than 25 whose moderate to severe sleep apnea has failed treatment with other, more established therapies. 

Since then, eligibility requirements have loosened, with the FDA now allowing the device to be used in patients with BMIs as high as 40 and Medicare providing coverage for patients with BMIs up to 35.

Landsness, a sleep researcher who treats patients with sleep apnea, was surprised by the changes in the eligibility criteria. To understand how the device performs in people of varying sizes, he and colleagues performed an independent evaluation using data from 78 people with BMIs up to 35 who received implants of the nerve-stimulation device at the Washington University Sleep Medicine Center from 2019 through 2023.

Impact on Treatment Efficacy

The primary study finding was that, overall, the device works. Three out of four patients showed significant improvement in apnea symptoms in the year following implantation. Most study participants experienced symptom reductions of at least 50%, with many showing dramatic reductions to near-normal or mild levels of sleep apnea.

However, among overweight study participants with BMIs of 32 to 35, the results were less positive, with the likelihood of successful treatment estimated to be 75% lower than those of study participants with lower BMIs.

“Body mass index is clearly an important factor in predicting whether hypoglossal nerve stimulation will work for an individual patient,” Landsness says in a release. “Our study shows an almost linear relationship between BMI and treatment success. For every unit of BMI increase over 32, the odds of successful treatment decrease by about 17%.”

Considerations for Treatment

Inspire is the only FDA-approved hypoglossal nerve-stimulation device available in the United States. The company also markets the device in Europe, Japan, and other countries. Tens of thousands of patients worldwide have been implanted with it.

Implantation of a hypoglossal nerve-stimulation device is a relatively simple outpatient surgery. Among the biggest concerns for patients are in terms of money and time. Landsness estimates that the therapy can cost from $50,000 to $100,000 out of pocket without insurance and take a year to be fully optimized.

“We have patients coming to us who really want this treatment because they view it as a life-changing alternative to CPAP,” Landsness says in a release. “It certainly can work for some people, but we don’t want to recommend it to patients if there’s a chance their BMIs will affect the device’s usefulness.”

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