Amyloid profile is associated with sleep quality in preclinical but not in prodromal Alzheimer’s disease older adults

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY
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Abstract

Background

Few studies have assessed whether neuropathological markers of AD in the preclinical and prodromal stages are associated with polysomnographic changes and obstructive sleep apnea (OSA).

Methods

This was a cross-sectional, case-control study of older adults (≥60 years) without relevant clinical and psychiatric comorbidities selected randomly from a cohort of individuals without dementia in a tertiary university hospital in São Paulo, Brazil. They underwent neuropsychological evaluation for clinical diagnosis and were allocated into two samples: cognitively unimpaired (CU) and mild cognitive impairment (MCI). Also, they underwent PET-PiB to determine the amyloid profile and all-night in-lab polysomnography. For each sample, we compared polysomnographic parameters according to the amyloid profile (A+ vs A-).

Results

We allocated 67 participants (mean age 73 years, SD 10,1), 70 % females, 14 ± 5 years of education, into two samples: CU (n = 28, 42.4 %) and MCI (n = 39, 57.6 %). In the CU sample, the group A+ (n = 9) showed worse sleep parameters than A- (n = 19) (lower total sleep time (p = 0.007), and sleep efficiency (p = 0.005); higher sleep onset latency (p = 0.025), wake time after sleep onset (p = 0.011), and arousal index (AI) (p = 0.007)), and changes in sleep structure: higher %N1 (p = 0.005), and lower %REM (p = 0.006). In the MCI sample, MCI A-had higher AI (p = 0.013), respiratory disturbance index (p = 0.025, controlled for age), and higher rates of severe OSA than A+.

Discussion

The amyloid profile was associated with polysomnographic markers of worse sleep quality in individuals with preclinical AD but not with prodromal AD, probably due to the higher frequencies of severe OSA.

淀粉样蛋白特征与临床前和原发性阿尔茨海默氏症老年人的睡眠质量有关。
很少有研究评估临床前和前驱阶段的老年痴呆症神经病理学标志物是否与多导睡眠图变化和阻塞性睡眠呼吸暂停(OSA)有关。这是一项横断面病例对照研究,研究对象是从巴西圣保罗一所三级大学医院的无痴呆症患者队列中随机挑选的无相关临床和精神疾病的老年人(≥60 岁)。他们接受了神经心理学评估以进行临床诊断,并被分为两个样本:认知功能未受损(CU)和轻度认知功能受损(MCI)。此外,他们还接受了 PET-PiB 检查以确定淀粉样蛋白谱,并接受了实验室内通宵多导睡眠图检查。我们根据淀粉样蛋白特征(A+ vs A-)对每个样本的多导睡眠图参数进行了比较。结果我们将 67 名参与者(平均年龄 73 岁,SD 10.1)分为两个样本,其中 70% 为女性,受教育年限为 14±5 年:CU(28 人,42.4%)和 MCI(39 人,57.6%)。在CU样本中,A+组(n=9)的睡眠参数比A-组(n=19)差(总睡眠时间(p=0.007)和睡眠效率(p=0.005)较低;睡眠开始潜伏期(p=0.025)、睡眠开始后唤醒时间(p=0.011)和唤醒指数(AI)(p=0.007)较高),睡眠结构也有变化:%N1(p=0.005)较高,%REM(p=0.006)较低。在 MCI 样本中,与 A+ 相比,MCI A- 的 AI(p=0.013)、呼吸紊乱指数(p=0.025,与年龄相关)和严重 OSA 的比率更高。淀粉样蛋白特征与临床前注意力缺失症患者睡眠质量较差的多导睡眠图标志物有关,但与前驱注意力缺失症无关,这可能是由于严重OSA的发生率较高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Sleep medicine
Sleep medicine 医学-临床神经学
CiteScore
8.40
自引率
6.20%
发文量
1060
审稿时长
49 days
期刊介绍: Sleep Medicine aims to be a journal no one involved in clinical sleep medicine can do without. A journal primarily focussing on the human aspects of sleep, integrating the various disciplines that are involved in sleep medicine: neurology, clinical neurophysiology, internal medicine (particularly pulmonology and cardiology), psychology, psychiatry, sleep technology, pediatrics, neurosurgery, otorhinolaryngology, and dentistry. The journal publishes the following types of articles: Reviews (also intended as a way to bridge the gap between basic sleep research and clinical relevance); Original Research Articles; Full-length articles; Brief communications; Controversies; Case reports; Letters to the Editor; Journal search and commentaries; Book reviews; Meeting announcements; Listing of relevant organisations plus web sites.
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