University of Massachusetts Medical School, Worcester, MA, USA.
Department of Neurology, Dysautonomia Center, New York University School of Medicine, New York, NY, USA.
Sleep Med. 2018 May;45:33-38. doi: 10.1016/j.sleep.2017.12.013. Epub 2018 Feb 7.
Familial dysautonomia (FD) is an autosomal recessive disorder characterized by impaired development of sensory and afferent autonomic nerves. Untreated sleep-disordered breathing (SDB) has been reported to increase the risk of sudden unexpected death in FD. We aimed to describe the prevalence and characteristics of SDB in FD.
PATIENTS/METHODS: Seventy-five patients with FD (20 adults and 55 children) underwent in-lab polysomnography, including peripheral capillary oxygen saturation (SpO) and end-tidal capnography (EtCO) measurements. A t-test and Spearman's correlation analysis were performed to evaluate the impact of age on sleep, occurrence of apneas, SpO and EtCO levels; and to determine the relationship between apneas and SpO/EtCO measurements during different sleep stages.
Overall, 85% of adults and 91% of pediatric patients had some degree of SDB. Obstructive sleep apneas were more severe in adults (8.5 events/h in adults vs. 3.5 events/h in children, p = 0.04), whereas central apneas were more severe (10.8 vs. 2.8 events/h, p = 0.04) and frequent (61.8% vs. 45%, p = 0.017) in children. Overall, a higher apnea-hypopnea index was associated with increased severity of hypoxia and hypoventilation, although in a significant fraction of patients (67% and 46%), hypoxemia and hypoventilation occurred independent of apneas.
Most adult and pediatric patients with FD suffer from some degree of SDB. There was a differential effect of age in the pattern of SDB observed. In some FD patients, hypoventilation and hypoxia occurred independently of apneas. Therefore, we recommend including EtCO monitoring during polysomnography in all patients with FD to detect SDB.
家族性自主神经机能异常(FD)是一种常染色体隐性遗传病,其特征为感觉和传入自主神经发育不良。未经治疗的睡眠呼吸障碍(SDB)已被报道会增加 FD 患者猝死的风险。我们旨在描述 FD 患者 SDB 的患病率和特征。
患者/方法:75 名 FD 患者(20 名成人和 55 名儿童)接受了实验室多导睡眠图检查,包括外周毛细血管血氧饱和度(SpO)和呼气末二氧化碳(EtCO)测量。采用 t 检验和斯皮尔曼相关性分析来评估年龄对睡眠、呼吸暂停发作、SpO 和 EtCO 水平的影响;并确定不同睡眠阶段呼吸暂停与 SpO/EtCO 测量值之间的关系。
总体而言,85%的成年患者和 91%的儿科患者存在不同程度的 SDB。成人的阻塞性睡眠呼吸暂停更为严重(成人 8.5 次/小时,儿童 3.5 次/小时,p=0.04),而儿童的中枢性呼吸暂停更为严重(10.8 次/小时,儿童 2.8 次/小时,p=0.04)且更为频繁(61.8%,儿童 45%,p=0.017)。总体而言,呼吸暂停低通气指数越高,缺氧和通气不足越严重,尽管在相当一部分患者(67%和 46%)中,低氧血症和通气不足与呼吸暂停无关。
大多数 FD 成年和儿科患者都存在不同程度的 SDB。年龄对 SDB 模式有不同的影响。在一些 FD 患者中,通气不足和缺氧与呼吸暂停无关。因此,我们建议在所有 FD 患者的多导睡眠图检查中纳入 EtCO 监测,以检测 SDB。