Comprehensive Epilepsy Program, Department of Neurology, University of Virginia, Charlottesville, VA, USA.
UVA Section of Geriatrics, School of Nursing, University of Virginia, Charlottesville, VA, USA.
J Alzheimers Dis. 2022;89(4):1367-1374. doi: 10.3233/JAD-220664.
While sleep disturbances appear to be risk factors in Alzheimer's disease (AD) progression, information such as the prevalence across dementia severity and the influence on the trajectory of cognitive decline is unclear.
We evaluate the hypotheses that the prevalence of insomnia differs by cognitive impairment, that sleep disturbances track with AD biomarkers, and that longitudinal changes in sleep disorders affect cognition.
We used the National Alzheimer's Coordinating Center Database to determine the prevalence of clinician-identified insomnia and nighttime behaviors in normal, mild cognitive impairment (MCI), and demented individuals. We evaluated mean Montreal Cognitive Assessment (MoCA) scores, hippocampal volumes (HV), and CSF phosphorylated tau:amyloid-β ratios at first visit using analysis of variance with age as a covariate. In longitudinal evaluations, we assessed changes in MoCA scores and HV in insomnia and nighttime behaviors between the first and last visits.
Prevalence of insomnia was 14%, 16%, and 11% for normal, MCI, and dementia groups. Prevalence of nighttime behaviors was 14%, 21%, and 29% respectively. Insomnia patients had higher MoCA scores, larger HV, and lower pTauBeta than individuals without insomnia, indicating less neurodegeneration. In contrast, nighttime behaviors were associated with worse cognition, smaller HV, and higher pTauBeta. Similar findings were seen between longitudinal associations of sleep disorders and cognition and HV.
Our findings suggest that insomnia is unreliably recognized in patients with cognitive impairment. Nighttime behaviors may better indicate the presence of sleep disturbances and have diagnostic specificity in AD over insomnia.
睡眠障碍似乎是阿尔茨海默病(AD)进展的危险因素,但关于其在痴呆严重程度中的患病率以及对认知能力下降轨迹的影响等信息尚不清楚。
我们评估了以下假设:失眠的患病率因认知障碍而异,睡眠障碍与 AD 生物标志物相关,以及睡眠障碍的纵向变化会影响认知。
我们使用国家阿尔茨海默病协调中心数据库来确定临床医生识别的失眠症和夜间行为在正常、轻度认知障碍(MCI)和痴呆个体中的患病率。我们使用方差分析评估了首次就诊时平均蒙特利尔认知评估(MoCA)评分、海马体积(HV)和 CSF 磷酸化 tau:淀粉样蛋白-β比值,以年龄为协变量。在纵向评估中,我们评估了失眠症和夜间行为在首次和最后一次就诊之间的 MoCA 评分和 HV 变化。
正常、MCI 和痴呆组的失眠症患病率分别为 14%、16%和 11%。夜间行为的患病率分别为 14%、21%和 29%。失眠症患者的 MoCA 评分较高、HV 较大、pTauBeta 较低,表明神经退行性病变较少。相比之下,夜间行为与认知和 HV 较差有关。睡眠障碍与认知和 HV 之间的纵向关联也存在类似的发现。
我们的研究结果表明,失眠症在认知障碍患者中可能无法可靠地识别。夜间行为可能更好地表明存在睡眠障碍,并且在 AD 中比失眠症更具有诊断特异性。