Yoon Dasoo M, Plante David T, Fleming Victoria, Handen Benjamin, Lao Patrick, Peven Jamie, Christian Bradley, Okonkwo Ozioma, Laymon Charles, Ances Beau, Hom Christy, Helsel Brian, Hartley Sigan L
Waisman Center, University of Wisconsin, Madison, Madison, WI 53705, United States.
Department of Human Development and Family Studies, University of Wisconsin, Madison 53705, United States.
Sleep Adv. 2025 Jul 23;6(3):zpaf044. doi: 10.1093/sleepadvances/zpaf044. eCollection 2025.
This study provided a preliminary examination of indices of obstructive sleep apsnea (OSA) and sleep disruptions in adults with Down syndrome (DS), and their associations with Alzheimer's disease (AD) pathology and symptomatology. A total of 93 adults with DS (aged 25-61 years) from the Alzheimer Biomarker Consortium-DS completed cognitive assessments, MRI and positron emission tomography (PET) scans (assessing amyloid-beta [Aβ] and tau), and a one-night home sleep study using the WatchPAT-300 device. Study partners also reported on depressive symptoms and diagnoses. Correlational analyses examined relationships between sleep variables, PET biomarkers, and AD symptomatology (cognitive functioning and depressive mood), controlling for sociodemographics. A total of 81 participants (87 per cent) completed valid WatchPAT data. Of these, 60 (74 per cent) screened positive for OSA, and an additional 11 had a prior OSA diagnosis and used CPAP during the test night. Nearly half (45 per cent) of those screening positive for OSA had no prior diagnosis, indicating under-detection. Among the 22 participants using OSA treatment, 50 per cent continued to show sleep-disordered breathing, suggesting suboptimal treatment effectiveness. Higher wake percentage and shorter total sleep time were associated with greater Aβ and tau burden. Cognitive performance was negatively associated with wake percentage, total sleep time, and oxygenation indices (minimum oxygen, desaturation, and time ≤ 88 per cent oxygen). Depressive symptoms were negatively related to total sleep time. These findings add preliminary evidence linking sleep disruption and OSA with AD-related pathology and symptomatology. Larger, longitudinal studies are needed to confirm these associations and evaluate whether improving sleep quality and treating OSA may help delay AD onset in this high-risk population.
本研究初步考察了唐氏综合征(DS)成人患者的阻塞性睡眠呼吸暂停(OSA)指标和睡眠中断情况,以及它们与阿尔茨海默病(AD)病理和症状的关联。来自阿尔茨海默病生物标志物联盟 - DS的93名DS成人患者(年龄25 - 61岁)完成了认知评估、MRI和正电子发射断层扫描(PET)(评估淀粉样蛋白β[Aβ]和tau),并使用WatchPAT - 300设备进行了一晚的家庭睡眠研究。研究伙伴还报告了抑郁症状和诊断情况。相关性分析考察了睡眠变量、PET生物标志物与AD症状(认知功能和抑郁情绪)之间的关系,并对社会人口统计学因素进行了控制。共有81名参与者(87%)完成了有效的WatchPAT数据。其中,60名(74%)筛查出OSA呈阳性,另有11名之前被诊断为OSA并在测试当晚使用持续气道正压通气(CPAP)。在筛查出OSA呈阳性的患者中,近一半(45%)之前未被诊断,表明存在漏诊情况。在22名接受OSA治疗的参与者中,50%仍表现出睡眠呼吸紊乱,提示治疗效果欠佳。较高的清醒百分比和较短的总睡眠时间与更大的Aβ和tau负荷相关。认知表现与清醒百分比、总睡眠时间和氧合指数(最低氧含量、血氧饱和度下降和血氧≤88%的时间)呈负相关。抑郁症状与总睡眠时间呈负相关。这些发现为睡眠中断和OSA与AD相关病理及症状之间的联系增添了初步证据。需要开展更大规模的纵向研究来证实这些关联,并评估改善睡眠质量和治疗OSA是否有助于延缓这一高危人群的AD发病。