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Proof of Concept Trial of Dronabinol in Obstructive Sleep Apnea
Study Objective: Animal data suggest that Δ(9)-TetraHydroCannabinol (Δ(9)THC) stabilizes autonomic output during sleep, reduces spontaneous sleep-disordered breathing, and blocks serotonin-induced exacerbation of sleep apnea. On this basis, we examined the safety, tolerability, and efficacy of drona...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3550518/ https://www.ncbi.nlm.nih.gov/pubmed/23346060 http://dx.doi.org/10.3389/fpsyt.2013.00001 |
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author | Prasad, Bharati Radulovacki, Miodrag G. Carley, David W. |
author_facet | Prasad, Bharati Radulovacki, Miodrag G. Carley, David W. |
author_sort | Prasad, Bharati |
collection | PubMed |
description | Study Objective: Animal data suggest that Δ(9)-TetraHydroCannabinol (Δ(9)THC) stabilizes autonomic output during sleep, reduces spontaneous sleep-disordered breathing, and blocks serotonin-induced exacerbation of sleep apnea. On this basis, we examined the safety, tolerability, and efficacy of dronabinol (Δ(9)THC), an exogenous Cannabinoid type 1 and type 2 (CB1 and CB2) receptor agonist in patients with Obstructive Sleep Apnea (OSA). Design and Setting: Proof of concept; single-center dose-escalation study of dronabinol. Participants: Seventeen adults with a baseline Apnea Hypopnea Index (AHI) ≥15/h. Baseline polysomnography (PSG) was performed after a 7-day washout of Continuous Positive Airway Pressure treatment. Intervention: Dronabinol was administered after baseline PSG, starting at 2.5 mg once daily. The dose was increased weekly, as tolerated, to 5 mg and finally to 10 mg once daily. Measurements and Results: Repeat PSG assessments were performed on nights 7, 14, and 21 of dronabinol treatment. Change in AHI (ΔAHI, mean ± SD) was significant from baseline to night 21 (−14.1 ± 17.5; p = 0.007). No degradation of sleep architecture or serious adverse events was noted. Conclusion: Dronabinol treatment is safe and well-tolerated in OSA patients at doses of 2.5–10 mg daily and significantly reduces AHI in the short-term. These findings should be confirmed in a larger study in order to identify sub-populations with OSA that may benefit from cannabimimetic pharmacologic therapy. |
format | Online Article Text |
id | pubmed-3550518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35505182013-01-23 Proof of Concept Trial of Dronabinol in Obstructive Sleep Apnea Prasad, Bharati Radulovacki, Miodrag G. Carley, David W. Front Psychiatry Psychiatry Study Objective: Animal data suggest that Δ(9)-TetraHydroCannabinol (Δ(9)THC) stabilizes autonomic output during sleep, reduces spontaneous sleep-disordered breathing, and blocks serotonin-induced exacerbation of sleep apnea. On this basis, we examined the safety, tolerability, and efficacy of dronabinol (Δ(9)THC), an exogenous Cannabinoid type 1 and type 2 (CB1 and CB2) receptor agonist in patients with Obstructive Sleep Apnea (OSA). Design and Setting: Proof of concept; single-center dose-escalation study of dronabinol. Participants: Seventeen adults with a baseline Apnea Hypopnea Index (AHI) ≥15/h. Baseline polysomnography (PSG) was performed after a 7-day washout of Continuous Positive Airway Pressure treatment. Intervention: Dronabinol was administered after baseline PSG, starting at 2.5 mg once daily. The dose was increased weekly, as tolerated, to 5 mg and finally to 10 mg once daily. Measurements and Results: Repeat PSG assessments were performed on nights 7, 14, and 21 of dronabinol treatment. Change in AHI (ΔAHI, mean ± SD) was significant from baseline to night 21 (−14.1 ± 17.5; p = 0.007). No degradation of sleep architecture or serious adverse events was noted. Conclusion: Dronabinol treatment is safe and well-tolerated in OSA patients at doses of 2.5–10 mg daily and significantly reduces AHI in the short-term. These findings should be confirmed in a larger study in order to identify sub-populations with OSA that may benefit from cannabimimetic pharmacologic therapy. Frontiers Media S.A. 2013-01-22 /pmc/articles/PMC3550518/ /pubmed/23346060 http://dx.doi.org/10.3389/fpsyt.2013.00001 Text en Copyright © 2013 Prasad, Radulovacki and Carley. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Psychiatry Prasad, Bharati Radulovacki, Miodrag G. Carley, David W. Proof of Concept Trial of Dronabinol in Obstructive Sleep Apnea |
title | Proof of Concept Trial of Dronabinol in Obstructive Sleep Apnea |
title_full | Proof of Concept Trial of Dronabinol in Obstructive Sleep Apnea |
title_fullStr | Proof of Concept Trial of Dronabinol in Obstructive Sleep Apnea |
title_full_unstemmed | Proof of Concept Trial of Dronabinol in Obstructive Sleep Apnea |
title_short | Proof of Concept Trial of Dronabinol in Obstructive Sleep Apnea |
title_sort | proof of concept trial of dronabinol in obstructive sleep apnea |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3550518/ https://www.ncbi.nlm.nih.gov/pubmed/23346060 http://dx.doi.org/10.3389/fpsyt.2013.00001 |
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