State-Dependent Biomechanical Behavior of Oropharyngeal Structures in Apneic and Control Subjects: A Proof-of-Concept Study
Apneic individuals have reduced airway caliber during sleep. The biomechanical changes in upper airway anatomy contributing to this airway narrowing are largely unknown. We sought to investigate the state-dependent (wake vs. sleep) biomechanical behavior of the upper airway soft-tissue and craniofac...
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Published in | Annals of the American Thoracic Society Vol. 21; no. 6; pp. 949 - 960 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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United States
American Thoracic Society
01.06.2024
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Abstract | Apneic individuals have reduced airway caliber during sleep. The biomechanical changes in upper airway anatomy contributing to this airway narrowing are largely unknown.
We sought to investigate the state-dependent (wake vs. sleep) biomechanical behavior of the upper airway soft-tissue and craniofacial structures.
Upper airway magnetic resonance imaging was performed in 15 sleep-deprived control subjects (apnea-hypopnea index, <5; 0.3 ± 0.5 events per hour) and 12 sleep-deprived apneic subjects (apnea-hypopnea index, ⩾5; 35.2 ± 18.1 events per hour) during wake and sleep and analyzed for airway measures and soft-tissue/mandibular movement.
In the retropalatal region, control subjects showed sleep-dependent reductions (
⩽ 0.037) in average cross-sectional airway area (CSA), minimum CSA, and anteroposterior and lateral dimensions. Apneic subjects showed sleep-dependent reductions (
⩽ 0.002) in average CSA, minimum CSA, and anteroposterior and lateral dimensions. In the retroglossal region, control subjects had no sleep-dependent airway reductions. However, apneic subjects had sleep-dependent reductions in minimal CSA (
= 0.001) and lateral dimensions (
= 0.014). Control subjects only showed sleep-dependent posterior movement of the anterior-inferior tongue octant (
= 0.039), whereas apneic subjects showed posterior movement of the soft palate (
= 0.006) and all tongue octants (
⩽ 0.012). Sleep-dependent medial movement of the lateral walls was seen at the retropalatal minimum level (
= 0.013) in control subjects and at the retropalatal and retroglossal minimum levels (
⩽ 0.017) in apneic subjects. There was posterior movement of the mandible in apneic subjects (
⩽ 0.017).
During sleep, control and apneic subjects showed reductions in retropalatal airway caliber, but only the apneic subjects showed retroglossal airway narrowing. Reductions in anteroposterior and lateral airway dimensions were primarily due to posterior soft palate, tongue and mandibular movement and to medial lateral wall movement. These data provide important initial insights into obstructive sleep apnea pathogenesis. |
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AbstractList | Schwab et al present a proof-of-concept study which aimed to investigate the state-dependent biomechanical behavior of the upper airway soft tissue and craniofacial structures in apneic and control subjects. Upper airway magnetic resonance imaging was performed in 15 control subjects and 12 apneic subjects during wake and sleep. The results showed that both groups exhibited reductions in airway caliber during sleep, with apneic subjects showing greater reductions compared to control subjects. The reductions in airway dimensions were primarily due to posterior movement of the soft palate, tongue, and mandible, as well as medial movement of the lateral pharyngeal walls. These findings provide important insights into the pathogenesis of obstructive sleep apnea and highlight the role of specific soft tissue and craniofacial structures in upper airway narrowing during sleep. Further studies with larger sample sizes are needed to confirm these findings and explore their implications for OSA treatment. Apneic individuals have reduced airway caliber during sleep. The biomechanical changes in upper airway anatomy contributing to this airway narrowing are largely unknown. We sought to investigate the state-dependent (wake vs. sleep) biomechanical behavior of the upper airway soft-tissue and craniofacial structures. Upper airway magnetic resonance imaging was performed in 15 sleep-deprived control subjects (apnea-hypopnea index, <5; 0.3 ± 0.5 events per hour) and 12 sleep-deprived apneic subjects (apnea-hypopnea index, ⩾5; 35.2 ± 18.1 events per hour) during wake and sleep and analyzed for airway measures and soft-tissue/mandibular movement. In the retropalatal region, control subjects showed sleep-dependent reductions ( ⩽ 0.037) in average cross-sectional airway area (CSA), minimum CSA, and anteroposterior and lateral dimensions. Apneic subjects showed sleep-dependent reductions ( ⩽ 0.002) in average CSA, minimum CSA, and anteroposterior and lateral dimensions. In the retroglossal region, control subjects had no sleep-dependent airway reductions. However, apneic subjects had sleep-dependent reductions in minimal CSA ( = 0.001) and lateral dimensions ( = 0.014). Control subjects only showed sleep-dependent posterior movement of the anterior-inferior tongue octant ( = 0.039), whereas apneic subjects showed posterior movement of the soft palate ( = 0.006) and all tongue octants ( ⩽ 0.012). Sleep-dependent medial movement of the lateral walls was seen at the retropalatal minimum level ( = 0.013) in control subjects and at the retropalatal and retroglossal minimum levels ( ⩽ 0.017) in apneic subjects. There was posterior movement of the mandible in apneic subjects ( ⩽ 0.017). During sleep, control and apneic subjects showed reductions in retropalatal airway caliber, but only the apneic subjects showed retroglossal airway narrowing. Reductions in anteroposterior and lateral airway dimensions were primarily due to posterior soft palate, tongue and mandibular movement and to medial lateral wall movement. These data provide important initial insights into obstructive sleep apnea pathogenesis. Rationale: Apneic individuals have reduced airway caliber during sleep. The biomechanical changes in upper airway anatomy contributing to this airway narrowing are largely unknown. Objectives: We sought to investigate the state-dependent (wake vs. sleep) biomechanical behavior of the upper airway soft-tissue and craniofacial structures. Methods: Upper airway magnetic resonance imaging was performed in 15 sleep-deprived control subjects (apnea-hypopnea index, <5; 0.3 ± 0.5 events per hour) and 12 sleep-deprived apneic subjects (apnea-hypopnea index, ⩾5; 35.2 ± 18.1 events per hour) during wake and sleep and analyzed for airway measures and soft-tissue/mandibular movement. Results: In the retropalatal region, control subjects showed sleep-dependent reductions (P ⩽ 0.037) in average cross-sectional airway area (CSA), minimum CSA, and anteroposterior and lateral dimensions. Apneic subjects showed sleep-dependent reductions (P ⩽ 0.002) in average CSA, minimum CSA, and anteroposterior and lateral dimensions. In the retroglossal region, control subjects had no sleep-dependent airway reductions. However, apneic subjects had sleep-dependent reductions in minimal CSA (P = 0.001) and lateral dimensions (P = 0.014). Control subjects only showed sleep-dependent posterior movement of the anterior-inferior tongue octant (P = 0.039), whereas apneic subjects showed posterior movement of the soft palate (P = 0.006) and all tongue octants (P ⩽ 0.012). Sleep-dependent medial movement of the lateral walls was seen at the retropalatal minimum level (P = 0.013) in control subjects and at the retropalatal and retroglossal minimum levels (P ⩽ 0.017) in apneic subjects. There was posterior movement of the mandible in apneic subjects (P ⩽ 0.017). Conclusions: During sleep, control and apneic subjects showed reductions in retropalatal airway caliber, but only the apneic subjects showed retroglossal airway narrowing. Reductions in anteroposterior and lateral airway dimensions were primarily due to posterior soft palate, tongue and mandibular movement and to medial lateral wall movement. These data provide important initial insights into obstructive sleep apnea pathogenesis.Rationale: Apneic individuals have reduced airway caliber during sleep. The biomechanical changes in upper airway anatomy contributing to this airway narrowing are largely unknown. Objectives: We sought to investigate the state-dependent (wake vs. sleep) biomechanical behavior of the upper airway soft-tissue and craniofacial structures. Methods: Upper airway magnetic resonance imaging was performed in 15 sleep-deprived control subjects (apnea-hypopnea index, <5; 0.3 ± 0.5 events per hour) and 12 sleep-deprived apneic subjects (apnea-hypopnea index, ⩾5; 35.2 ± 18.1 events per hour) during wake and sleep and analyzed for airway measures and soft-tissue/mandibular movement. Results: In the retropalatal region, control subjects showed sleep-dependent reductions (P ⩽ 0.037) in average cross-sectional airway area (CSA), minimum CSA, and anteroposterior and lateral dimensions. Apneic subjects showed sleep-dependent reductions (P ⩽ 0.002) in average CSA, minimum CSA, and anteroposterior and lateral dimensions. In the retroglossal region, control subjects had no sleep-dependent airway reductions. However, apneic subjects had sleep-dependent reductions in minimal CSA (P = 0.001) and lateral dimensions (P = 0.014). Control subjects only showed sleep-dependent posterior movement of the anterior-inferior tongue octant (P = 0.039), whereas apneic subjects showed posterior movement of the soft palate (P = 0.006) and all tongue octants (P ⩽ 0.012). Sleep-dependent medial movement of the lateral walls was seen at the retropalatal minimum level (P = 0.013) in control subjects and at the retropalatal and retroglossal minimum levels (P ⩽ 0.017) in apneic subjects. There was posterior movement of the mandible in apneic subjects (P ⩽ 0.017). Conclusions: During sleep, control and apneic subjects showed reductions in retropalatal airway caliber, but only the apneic subjects showed retroglossal airway narrowing. Reductions in anteroposterior and lateral airway dimensions were primarily due to posterior soft palate, tongue and mandibular movement and to medial lateral wall movement. These data provide important initial insights into obstructive sleep apnea pathogenesis. |
Author | Wehrli, Felix W. Lin, Theodore C. Wiemken, Andrew Keenan, Brendan T. Dedhia, Raj C. Schwab, Richard J. |
Author_xml | – sequence: 1 givenname: Richard J. surname: Schwab fullname: Schwab, Richard J. organization: Division of Sleep Medicine, Department of Medicine – sequence: 2 givenname: Theodore C. surname: Lin fullname: Lin, Theodore C. organization: Division of Sleep Medicine, Department of Medicine,, Department of Otorhinolaryngology – Head and Neck Surgery, Temple University, Philadelphia, Pennsylvania – sequence: 3 givenname: Andrew surname: Wiemken fullname: Wiemken, Andrew organization: Division of Sleep Medicine, Department of Medicine – sequence: 4 givenname: Raj C. surname: Dedhia fullname: Dedhia, Raj C. organization: Division of Sleep Medicine, Department of Medicine,, Department of Otorhinolaryngology – Head and Neck Surgery, and – sequence: 5 givenname: Felix W. surname: Wehrli fullname: Wehrli, Felix W. organization: Laboratory for Structural, Physiologic, and Functional Imaging, Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania; and – sequence: 6 givenname: Brendan T. orcidid: 0000-0002-9070-847X surname: Keenan fullname: Keenan, Brendan T. organization: Division of Sleep Medicine, Department of Medicine |
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Snippet | Apneic individuals have reduced airway caliber during sleep. The biomechanical changes in upper airway anatomy contributing to this airway narrowing are... Schwab et al present a proof-of-concept study which aimed to investigate the state-dependent biomechanical behavior of the upper airway soft tissue and... Rationale: Apneic individuals have reduced airway caliber during sleep. The biomechanical changes in upper airway anatomy contributing to this airway narrowing... |
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SubjectTerms | Adult Airway management Biomechanical Phenomena Case-Control Studies Clinical trials Female Humans Magnetic Resonance Imaging Male Medical treatment Middle Aged Original Research Oropharynx - diagnostic imaging Oropharynx - physiopathology Palate, Soft - diagnostic imaging Palate, Soft - physiopathology Polysomnography Proof of Concept Study Sleep - physiology Sleep apnea Sleep Apnea, Obstructive - physiopathology Tomography Tongue - diagnostic imaging Tongue - physiopathology |
Title | State-Dependent Biomechanical Behavior of Oropharyngeal Structures in Apneic and Control Subjects: A Proof-of-Concept Study |
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