# Redefining Obstructive Sleep Apnea: Treatment in the Modern Era

**Authors:** Jose Redondo, Kori B. Ascher, Alexandre R. Abreu

PMC · DOI: 10.3390/pathophysiology33010020 · Pathophysiology · 2026-03-02

## TL;DR

This paper reviews modern treatment options for obstructive sleep apnea beyond CPAP, highlighting new therapies that offer better adherence and personalized care.

## Contribution

The paper introduces a shift toward precision-based, multimodal treatment strategies for obstructive sleep apnea.

## Key findings

- Mandibular advancement devices and maxillomandibular advancement show durable improvements in OSA severity.
- GLP-1-based therapies like tirzepatide significantly reduce AHI and cardiometabolic risk in obesity-related OSA.
- Hypoglossal nerve stimulation provides durable benefits with high adherence, supported by multiple trial types.

## Abstract

Background: Obstructive sleep apnea (OSA) is a highly prevalent and heterogeneous disorder associated with substantial cardiometabolic morbidity. Although continuous positive airway pressure (CPAP) remains first-line therapy, long-term effectiveness is frequently limited by suboptimal adherence. Advances in airway devices, surgical techniques, neuromodulation, and pharmacologic therapies have expanded the therapeutic landscape and created opportunities for individualized, mechanism-based treatment. Methods: We conducted a selective, narrative review with structured quantitative synthesis of randomized controlled trials, comparative cohorts, long-term follow-up studies, registries, and mechanistic investigations addressing OSA therapies beyond CPAP. Evidence spanning oral appliances, upper-airway and skeletal surgery, hypoglossal nerve stimulation, neuromuscular electrical stimulation, positional therapy, and pharmacologic interventions targeting metabolic and non-anatomical endotypes was integrated. Outcomes of interest included apnea–hypopnea index (AHI), oxygenation, blood pressure, patient-reported symptoms, durability, safety, and real-world adherence. Results: Mandibular advancement devices (MADs) consistently reduced AHI relative to placebo and produced symptom relief comparable to CPAP in mild-to-moderate OSA, largely due to superior adherence. Palatal surgery yielded meaningful short-term improvement in selected patients but demonstrated limited long-term durability. In contrast, maxillomandibular advancement (MMA) achieved the largest and most durable reductions in OSA severity, with efficacy comparable to CPAP and superior to other surgical modalities in appropriate skeletal phenotypes. Hypoglossal nerve stimulation (HNS) produced substantial, durable improvements in AHI and symptoms with high adherence, supported by randomized trials, long-term follow-up, and real-world registry data; newer bilateral and proximal stimulation systems may further broaden candidacy. Neuromuscular electrical stimulation and positional therapy provided modest, phenotype-dependent benefits, primarily as adjunctive or early-stage interventions. A major advance is the emergence of metabolic and endotype-targeted pharmacotherapy: longitudinal data demonstrate a dose-dependent relationship between weight change and OSA progression or regression, while randomized trials show that GLP-1-based therapies—particularly dual GLP-1/GIP agonism with tirzepatide—produce large, clinically meaningful reductions in AHI and cardiometabolic risk in obesity-associated OSA. Additional pharmacologic strategies targeting ventilatory loop gain and arousal threshold further support an endotype-driven treatment paradigm. Conclusions: Contemporary OSA management is shifting from a CPAP-centric model toward a precision-guided, multimodal framework that aligns therapy with dominant anatomic and physiological contributors to airway collapse. Integrating metabolic, neuromodulatory, and structural interventions—often in combination—offers the potential for durable disease control and improved patient-centered outcomes. Future priorities include head-to-head and combination trials, long-term cardiovascular outcomes, cost-effectiveness analyses, and pragmatic tools to operationalize personalized OSA therapy in routine clinical practice.

## Linked entities

- **Chemicals:** tirzepatide (PubChem CID 163285897)
- **Diseases:** obstructive sleep apnea (MONDO:0007147)

## Full-text entities

- **Genes:** GIP (gastric inhibitory polypeptide) [NCBI Gene 2695], GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}
- **Diseases:** obesity hypoventilation (MESH:D010845), Sleepiness (MESH:D000077260), SCALE Sleep Apnea (MESH:D012891), Weight gain (MESH:D015430), MMA (MESH:D020178), fragmentation (MESH:D012892), occlusal abnormalities (MESH:D001157), malocclusion (MESH:D008310), Weight Loss (MESH:D015431), HNS (MESH:D020437), fibrosis (MESH:D005355), airway restriction (MESH:D002313), neuromuscular tongue weakness (MESH:D014062), insomnia (MESH:D007319), central sleep apnea (MESH:D020182), ODI (MESH:D000860), temporomandibular joint (TMJ) pain or stiffness (MESH:D013706), cardiometabolic disease (MESH:D024821), fatigue (MESH:D005221), hypertension (MESH:D006973), kidney stone (MESH:D007669), appetite (MESH:D001068), macroglossia (MESH:D008260), PAP (MESH:D000402), hypoxic (MESH:D002534), craniofacial abnormalities (MESH:D019465), AHI (MESH:D020181), adiposity (MESH:D018205), oropharyngeal obstruction (MESH:D009959), skin irritation (MESH:D012871), hyperventilation (MESH:D006985), swelling (MESH:D004487), Respiratory disturbance (MESH:D012131), taste alterations (MESH:D004408), bleeding (MESH:D006470), infection (MESH:D007239), paresthesia (MESH:D010292), upper airway muscle suppression (MESH:C000726767), injury to (MESH:D014947), NMES (MESH:D004556), hypoventilation (MESH:D007040), tongue soreness (MESH:D014060), palatal obstruction (MESH:D002972), excessive daytime sleepiness (MESH:D006970), apnea (MESH:D001049), postoperative (MESH:D019106), metabolic acidosis (MESH:D000138), velopharyngeal dysfunction (MESH:D014681), dry mouth (MESH:D014987), Obesity (MESH:D009765), type 2 diabetes (MESH:D003924), acidemia (MESH:C537358), CSA (MESH:D003057), snoring (MESH:D012913), diabetes complications (MESH:D048909), weight regain (MESH:D055191), epilepsy (MESH:D004827), CAIs (MESH:C536058), postoperative pain (MESH:D010149), cognitive impairment (MESH:D003072)
- **Chemicals:** ice (MESH:D007053), titanium (MESH:D014025), bicarbonate (MESH:D001639), Sulthiame (MESH:C084593), nitrogen (MESH:D009584), H2O (MESH:D014867), MMA (-), zolpidem (MESH:D000077334), APAP (MESH:D000082), silicone (MESH:D012828), oxygen (MESH:D010100), AZM (MESH:D000086), Eszopiclone (MESH:D000069582), benzodiazepine (MESH:D001569)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13029657/full.md

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13029657/full.md

## References

123 references — full list in the complete paper: https://tomesphere.com/paper/PMC13029657/full.md

---
Source: https://tomesphere.com/paper/PMC13029657