TY - JOUR
T1 - Effects of tiagabine on slow wave sleep and arousal threshold in patients with obstructive sleep apnea
AU - Taranto-Montemurro, Luigi
AU - Sands, Scott A.
AU - Edwards, Bradley A.
AU - Azarbarzin, Ali
AU - Marques, Melania
AU - de Melo, Camila M.
AU - Eckert, Danny J.
AU - White, David P.
AU - Wellman, Andrew
PY - 2017/2/1
Y1 - 2017/2/1
N2 - Introduction: Obstructive sleep apnea (OSA) severity is markedly reduced during slow-wave sleep (SWS) even in patients with a severe disease. The reason for this improvement is uncertain but likely relates to non-anatomical factors (i.e. reduced arousability, chemosensitivity, and increased dilator muscle activity). The anticonvulsant tiagabine produces a dose-dependent increase in SWS in subjects without OSA. This study aimed to test the hypothesis that tiagabine would reduce OSA severity by raising the overall arousal threshold during sleep. Aims and Methods: After a baseline physiology night to assess patients' OSA phenotypic traits, a placebo-controlled, double-blind, crossover trial of tiagabine 12 mg administered before sleep was performed in 14 OSA patients. Under each condition, we assessed the effects on sleep and OSA severity using standard clinical polysomnography. Results: Tiagabine increased slow-wave activity (SWA) of the electroencephalogram (1-4 Hz) compared to placebo (1.8 [0.4] vs. 2.0 [0.5] Log?V2, p = .04) but did not reduce OSA severity (apnea-hypopnea index [AHI] 41.5 [20.3] vs. 39.1 [16.5], p > .5). SWS duration (25 [20] vs. 26 [43] mins, p > .5) and arousal threshold (?26.5 [5.0] vs. ?27.6 [5.1] cmH2O, p = .26) were also unchanged between nights. Conclusions: Tiagabine modified sleep microstructure (increase in SWA) but did not change the duration of SWS, OSA severity, or arousal threshold in this group of OSA patients. Based on these findings, tiagabine should not be considered as a therapeutic option for OSA treatment.
AB - Introduction: Obstructive sleep apnea (OSA) severity is markedly reduced during slow-wave sleep (SWS) even in patients with a severe disease. The reason for this improvement is uncertain but likely relates to non-anatomical factors (i.e. reduced arousability, chemosensitivity, and increased dilator muscle activity). The anticonvulsant tiagabine produces a dose-dependent increase in SWS in subjects without OSA. This study aimed to test the hypothesis that tiagabine would reduce OSA severity by raising the overall arousal threshold during sleep. Aims and Methods: After a baseline physiology night to assess patients' OSA phenotypic traits, a placebo-controlled, double-blind, crossover trial of tiagabine 12 mg administered before sleep was performed in 14 OSA patients. Under each condition, we assessed the effects on sleep and OSA severity using standard clinical polysomnography. Results: Tiagabine increased slow-wave activity (SWA) of the electroencephalogram (1-4 Hz) compared to placebo (1.8 [0.4] vs. 2.0 [0.5] Log?V2, p = .04) but did not reduce OSA severity (apnea-hypopnea index [AHI] 41.5 [20.3] vs. 39.1 [16.5], p > .5). SWS duration (25 [20] vs. 26 [43] mins, p > .5) and arousal threshold (?26.5 [5.0] vs. ?27.6 [5.1] cmH2O, p = .26) were also unchanged between nights. Conclusions: Tiagabine modified sleep microstructure (increase in SWA) but did not change the duration of SWS, OSA severity, or arousal threshold in this group of OSA patients. Based on these findings, tiagabine should not be considered as a therapeutic option for OSA treatment.
KW - sleep apnoea
KW - Sleep-disordered breathing
KW - tiagabine
KW - slow-wave sleep
KW - Arousal threshold
KW - Tiagabine
KW - Slow-wave sleep
UR - http://purl.org/au-research/grants/NHMRC/1035115
UR - http://purl.org/au-research/grants/NHMRC/1053201
UR - http://purl.org/au-research/grants/NHMRC/1049814
UR - http://www.scopus.com/inward/record.url?scp=85014062311&partnerID=8YFLogxK
U2 - 10.1093/sleep/zsw047
DO - 10.1093/sleep/zsw047
M3 - Article
SN - 0161-8105
VL - 40
JO - Sleep
JF - Sleep
IS - 2
M1 - zsw047
ER -