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O026 Effect of oral appliance therapy on OSA endotypes
INTRODUCTION: Long term CPAP therapy alters OSA endotypes (e.g., reduces loop gain and the arousal threshold). However, while oral appliance therapy (OAT) is known to improve upper airway collapsibility, its effects on non-anatomical OSA endotypes are unclear. METHODS: To investigate the effects of...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108917/ http://dx.doi.org/10.1093/sleepadvances/zpac029.025 |
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author | Osman, A Naik, G Tong, B Chiang, A Pinczel, A Rawson, G Donegan, M Pitcher, G Kwan, B Mukherjee, S Teare, A Eckert, D |
author_facet | Osman, A Naik, G Tong, B Chiang, A Pinczel, A Rawson, G Donegan, M Pitcher, G Kwan, B Mukherjee, S Teare, A Eckert, D |
author_sort | Osman, A |
collection | PubMed |
description | INTRODUCTION: Long term CPAP therapy alters OSA endotypes (e.g., reduces loop gain and the arousal threshold). However, while oral appliance therapy (OAT) is known to improve upper airway collapsibility, its effects on non-anatomical OSA endotypes are unclear. METHODS: To investigate the effects of OAT on polysomnographic estimates of OSA endotypes we studied 102 people with OSA (AHI=34±20 events/h) pre vs. post-treatment (following 4-6 weeks OAT acclimatization). AHI and endotypic traits were compared between the diagnostic and OAT study visits. RESULTS: OAT reduced the AHI by ~50% (30 [25-39] vs. 15 [12-19], median, 95% confidence interval, p<0.01). Passive pharyngeal collapsibility (94 [92-95] vs. 96 [95-97]% eupnea), active pharyngeal collapsibility (98 [95-100] vs. 102 [101-103]% eupnea) and pharyngeal muscle compensation (3.6 [1.2-5.1] vs 4.9 [3.7-6.5]% eupnea) improved with OAT (all p<0.01). The respiratory arousal threshold (116 [114-122] vs. 109 [106-111]% eupnea, p<0.01) and ventilatory response to arousal (31 [28-35] vs. 23 [20-32]% eupnea, p=0.03) decreased. Loop gain did not systematically change overall (0.43 [0.39-0.47] vs. 0.40 [0.38-0.42], p=0.16). However, loop gain reduced in OAT responders (>50% reduction in AHI) (0.42 [0.39-0.45] vs. 0.38 [0.34-0.4] dimensionless, p<0.01). CONCLUSIONS: Oral appliance therapy improves upper airway collapsibility and pharyngeal muscle compensation and reduces the ventilatory response to arousal and loop gain in responders. Like CPAP, OAT also decreases the arousal threshold. These findings provide new insight into the mechanisms of improvement in OSA with oral appliance therapy. |
format | Online Article Text |
id | pubmed-10108917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-101089172023-05-15 O026 Effect of oral appliance therapy on OSA endotypes Osman, A Naik, G Tong, B Chiang, A Pinczel, A Rawson, G Donegan, M Pitcher, G Kwan, B Mukherjee, S Teare, A Eckert, D Sleep Adv ORAL PRESENTATIONS INTRODUCTION: Long term CPAP therapy alters OSA endotypes (e.g., reduces loop gain and the arousal threshold). However, while oral appliance therapy (OAT) is known to improve upper airway collapsibility, its effects on non-anatomical OSA endotypes are unclear. METHODS: To investigate the effects of OAT on polysomnographic estimates of OSA endotypes we studied 102 people with OSA (AHI=34±20 events/h) pre vs. post-treatment (following 4-6 weeks OAT acclimatization). AHI and endotypic traits were compared between the diagnostic and OAT study visits. RESULTS: OAT reduced the AHI by ~50% (30 [25-39] vs. 15 [12-19], median, 95% confidence interval, p<0.01). Passive pharyngeal collapsibility (94 [92-95] vs. 96 [95-97]% eupnea), active pharyngeal collapsibility (98 [95-100] vs. 102 [101-103]% eupnea) and pharyngeal muscle compensation (3.6 [1.2-5.1] vs 4.9 [3.7-6.5]% eupnea) improved with OAT (all p<0.01). The respiratory arousal threshold (116 [114-122] vs. 109 [106-111]% eupnea, p<0.01) and ventilatory response to arousal (31 [28-35] vs. 23 [20-32]% eupnea, p=0.03) decreased. Loop gain did not systematically change overall (0.43 [0.39-0.47] vs. 0.40 [0.38-0.42], p=0.16). However, loop gain reduced in OAT responders (>50% reduction in AHI) (0.42 [0.39-0.45] vs. 0.38 [0.34-0.4] dimensionless, p<0.01). CONCLUSIONS: Oral appliance therapy improves upper airway collapsibility and pharyngeal muscle compensation and reduces the ventilatory response to arousal and loop gain in responders. Like CPAP, OAT also decreases the arousal threshold. These findings provide new insight into the mechanisms of improvement in OSA with oral appliance therapy. Oxford University Press 2022-11-09 /pmc/articles/PMC10108917/ http://dx.doi.org/10.1093/sleepadvances/zpac029.025 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Sleep Research Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | ORAL PRESENTATIONS Osman, A Naik, G Tong, B Chiang, A Pinczel, A Rawson, G Donegan, M Pitcher, G Kwan, B Mukherjee, S Teare, A Eckert, D O026 Effect of oral appliance therapy on OSA endotypes |
title | O026 Effect of oral appliance therapy on OSA endotypes |
title_full | O026 Effect of oral appliance therapy on OSA endotypes |
title_fullStr | O026 Effect of oral appliance therapy on OSA endotypes |
title_full_unstemmed | O026 Effect of oral appliance therapy on OSA endotypes |
title_short | O026 Effect of oral appliance therapy on OSA endotypes |
title_sort | o026 effect of oral appliance therapy on osa endotypes |
topic | ORAL PRESENTATIONS |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108917/ http://dx.doi.org/10.1093/sleepadvances/zpac029.025 |
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