Respiratory Trials·org

Sleep medicine · Treating the obesity rather than the airway

SURMOUNT-OSA

Tirzepatide for the Treatment of Obstructive Sleep Apnea and Obesity

SURMOUNT-OSA trial design and results
Design Two phase 3, double-blind, placebo-controlled trials
Treatment Tirzepatide
Control Placebo
Population Adults with moderate-to-severe obstructive sleep apnoea and obesity; mean baseline AHI 51.5 and 49.5 events per hour, mean BMI 39.1 and 38.7
Follow-up 52 weeks
Primary endpoint Change in apnoea-hypopnoea index at week 52
Result In trial 1 the AHI fell by 25.3 events per hour (95% CI -29.3 to -21.2) with tirzepatide versus 5.3 (-9.4 to -1.1) with placebo. Body weight, hypoxic burden, hsCRP and systolic blood pressure all fell, and sleep-related patient-reported outcomes improved.
Secondary endpoints Body weight, hypoxic burden, hsCRP, systolic blood pressure, patient-reported sleep outcomes

Among persons with moderate-to-severe obstructive sleep apnea and obesity, tirzepatide reduced the AHI, body weight, hypoxic burden, hsCRP concentration, and systolic blood pressure and improved sleep-related patient-reported outcomes.

The trial authors, in the published abstract

How it has aged

Reframes obstructive sleep apnoea in obesity as a treatable metabolic disease rather than a purely mechanical one. Halving the AHI with a drug, alongside falls in blood pressure and inflammatory markers, is a different proposition from splinting the airway — and, unlike SAVE, adherence is not the limiting factor.

Publications

Tirzepatide for the Treatment of Obstructive Sleep Apnea and Obesity

Malhotra A, Grunstein RR, Fietze I, et al. Tirzepatide for the Treatment of Obstructive Sleep Apnea and Obesity. N Engl J Med 2024 Oct 3;391(13):1193-1205.

  • AHI reduced by around 25 events per hour versus 5 with placebo
  • Weight, hypoxic burden, hsCRP and systolic blood pressure all improved
  • Patient-reported sleep outcomes improved