The obstructive sleep apnoea endotypes are similar in elderly trauma-exposed veterans with and without diagnosed PTSD

被引:1
|
作者
Brooker, Elliot J. [1 ]
Landry, Shane A. [2 ]
Mann, Dwayne [3 ]
Prguda, Emina [4 ,5 ]
Mcleay, Sarah C. [4 ]
Drummond, Sean P. A. [1 ]
Edwards, Bradley A. [1 ,6 ]
机构
[1] Monash Univ, Turner Inst Brain & Mental Hlth, Sch Psychol Sci, Clayton, Vic 3800, Australia
[2] Monash Univ, Biomed Discovery Inst, Dept Physiol, Clayton, Vic 3800, Australia
[3] Univ Queensland, Sch Elect Engn & Comp Sci, Brisbane, Qld 4072, Australia
[4] Gallipoli Med Res Fdn, Brisbane, Qld, Australia
[5] Univ Queensland, Brisbane, Qld 4006, Australia
[6] 1-270 Ferntree Gully Rd, Notting Hill, Vic 3168, Australia
关键词
Obstructive sleep apnoea; Post-traumatic stress disorder; Endotype; Pathophysiology; POSTTRAUMATIC-STRESS-DISORDER; AUSTRALIAN VIETNAM VETERANS; PHYSIOLOGICAL TRAITS; PREVALENCE; ADHERENCE; INSOMNIA; THERAPY; AROUSAL; ANXIETY; IMPACT;
D O I
10.1016/j.sleep.2024.02.006
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Approximately 60% of veterans living with posttraumatic stress disorder (PTSD) experience obstructive sleep apnoea (OSA). Why OSA is so prevalent in individuals with PTSD remains unknown, though PTSD may influence the underlying endotypes known to cause OSA. We examined whether these endotypes (upper airway collapsibility, muscle compensation, loop gain, and the arousal threshold) differ between those with comorbid OSA and PTSD relative to their counterparts with OSA-only. Methods: Using the ventilatory flow pattern from diagnostic polysomnography, the OSA endotypes were measured in a retrospective cohort of 21 OSA patients with PTSD and 27 OSA-only patients. All participants were trauma exposed elderly male Australian Vietnam War veterans with mild -to -severe OSA (median ApnoeaHypopnea index: 20.2 vs. 23.6 events/h). Age and BMI were similar between groups (70.7 vs. 71.7 years, and 28.4 vs. 28.4 kg/m2). Results: There were no significant differences in the OSA endotype traits between PTSD + OSA and OSA-only patients for upper airway collapsibility (76.68 [71.53-83.56] vs. 78.35 [72.81-83.82] %Veupnea, median [IQR]), muscle compensation (4.27 [0.34-9.18] vs. 5.41 [1.83-7.21] %Veupnea), loop gain (0.56(0.17) vs. 0.60 (0.14)), and arousal threshold (135.76 [126.59-147.54] vs. 146.95 [128.64-151.28] %Veupnea). Conclusion: The OSA endotypes in veterans with PTSD were similar to their trauma exposed OSA-only counterparts. PTSD appears to exert little influence on the OSA endotypes beyond the effect that age and trauma exposure may have. The aetiology of increased prevalence of OSA in PTSD remains unclear. Further work examining OSA endotypes using larger and more diverse samples is needed before robust conclusions can be made.
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页码:48 / 54
页数:7
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