Qu Xin Ru, Cheng Zi Qian, Li Yi Ming, Han Teng, Zhang Xiao Lei
Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, China-Japan Friendship Hospital, Beijing, China.
Sci Rep. 2025 May 8;15(1):16050. doi: 10.1038/s41598-025-00385-9.
Obstructive sleep apnea (OSA) is associated with an increased prevalence of aortic aneurysm, but the impact of OSA on the subclinical damage of large thoracic vessels remains controversial. Short sleep duration and poor sleep quality has been reported to be related with higher arterial stiffness. In the current study, we aimed to investigate the association of sleep disturbance and sleep apnea with the size of the ascending aorta (AA), descending thoracic aorta (DTA), and main pulmonary artery (MPA). One hundred and fifty-five newly diagnosed OSA patients free of cardiovascular disease and medication were included. In-laboratory polysomnography (PSG) and chest computed tomography (CT) scanning were performed. The sleep duration was defined as total sleep time (TST) as recorded during overnight PSG, with TST < 6 h defined as short sleep duration. Sleep latency (SL), sleep efficiency (SE) and wake after sleep onset (WASO) were used to assess the objective sleep quality, and the Epworth Sleepiness Scale (ESS) was used to assess EDS (excessive daytime sleepiness). The diameter of AA was positively associated with age (B = 0.199, P < 0.001) and diastolic blood pressure (DBP) (B = 0.103, P < 0.001), and was negatively associated with mean pulse oxygen saturation (SpOmean) (B = - 0.176, P = 0.022). The diameter of DTA was positively associated with age (B = 0.112, P < 0.001), body mass index (BMI) (B = 0.184, P = 0.041), and DBP (B = 0.033, P = 0.024), and was negatively associated with TST (B = - 0.006, P = 0.023). Neither nocturnal hypoxia nor TST were associated with the diameter of MPA or the ratio of MPA to AA (PA/A). The aortic or MPA measurements were not associated with SL, SE, WASO or ESS. In patients with OSA, nocturnal hypoxia and sleep duration were associated with the diameter of AA and DTA, respectively. It is suggested that sleep apnea and sleep disturbance may exert effects on the remodeling and enlargement of thoracic large vessels through distinctive mechanisms.
阻塞性睡眠呼吸暂停(OSA)与主动脉瘤患病率增加相关,但OSA对大胸段血管亚临床损伤的影响仍存在争议。据报道,睡眠时间短和睡眠质量差与较高的动脉僵硬度有关。在本研究中,我们旨在调查睡眠障碍和睡眠呼吸暂停与升主动脉(AA)、降胸主动脉(DTA)和主肺动脉(MPA)大小之间的关联。纳入了155例新诊断的无心血管疾病且未服用药物的OSA患者。进行了实验室多导睡眠图(PSG)和胸部计算机断层扫描(CT)。睡眠时间定义为夜间PSG记录的总睡眠时间(TST),TST < 6小时定义为睡眠时间短。睡眠潜伏期(SL)、睡眠效率(SE)和睡眠中觉醒时间(WASO)用于评估客观睡眠质量,Epworth嗜睡量表(ESS)用于评估日间过度嗜睡(EDS)。AA直径与年龄(B = 0.199,P < 0.001)和舒张压(DBP)(B = 0.103,P < 0.001)呈正相关,与平均脉搏血氧饱和度(SpOmean)(B = -0.176,P = 0.022)呈负相关。DTA直径与年龄(B = 0.112,P < 0.001)、体重指数(BMI)(B = 0.184,P = 0.041)和DBP(B = 0.033,P = 0.024)呈正相关,与TST(B = -0.006,P = 0.023)呈负相关。夜间低氧和TST均与MPA直径或MPA与AA的比值(PA/A)无关。主动脉或MPA测量值与SL、SE、WASO或ESS无关。在OSA患者中,夜间低氧和睡眠时间分别与AA和DTA直径相关。提示睡眠呼吸暂停和睡眠障碍可能通过独特机制对胸段大血管的重塑和扩张产生影响。