Faculty of Health, Medicine and Life Sciences, School for Mental Health and Neuroscience, Alzheimer Centre Limburg, Maastricht University, Maastricht, The Netherlands.
Department of Sleep and Cognition, Netherlands Institute for Neuroscience, Institute of the Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands.
Ann Neurol. 2024 Apr;95(4):653-664. doi: 10.1002/ana.26880. Epub 2024 Feb 26.
While studies suggested that locus coeruleus (LC) neurodegeneration contributes to sleep-wake dysregulation in Alzheimer's disease (AD), the association between LC integrity and circadian rest-activity patterns remains unknown. Here, we investigated the relationships between 24-hour rest-activity rhythms, cognitive trajectories, and autopsy-derived LC integrity in older adults with and without cortical AD neuropathology.
This retrospective study leveraged multi-modal data from participants of the longitudinal clinical-pathological Rush Memory and Aging Project. Indices of 24-hour rest-activity rhythm fragmentation (intradaily variability) and stability (interdaily stability) were extracted from annual actigraphic recordings, and cognitive trajectories were computed from annual cognitive evaluations. At autopsy, LC neurodegeneration was determined by the presence of hypopigmentation, and cortical AD neuropathology was assessed. Contributions of comorbid pathologies (Lewy bodies, cerebrovascular pathology) were evaluated.
Among the 388 cases included in the study sample (age at death = 92.1 ± 5.9 years; 273 women), 98 (25.3%) displayed LC hypopigmentation, and 251 (64.7%) exhibited cortical AD neuropathology. Logistic regression models showed that higher rest-activity rhythm fragmentation, measured up to ~7.1 years before death, was associated with increased risk to display LC neurodegeneration at autopsy (odds ratio [OR] = 1.46, 95% confidence interval [CI]: 1.16-1.84, p = 0.004), particularly in individuals with cortical AD neuropathology (OR = 1.56, CI: 1.15-2.15, p = 0.03) and independently of comorbid pathologies. In addition, longitudinal increases in rest-activity rhythm fragmentation partially mediated the association between LC neurodegeneration and cognitive decline (estimate = -0.011, CI: -0.023--0.002, p = 0.03).
These findings highlight the LC as a neurobiological correlate of sleep-wake dysregulation in AD, and further underscore the clinical relevance of monitoring rest-activity patterns for improved detection of at-risk individuals. ANN NEUROL 2024;95:653-664.
虽然有研究表明蓝斑(LC)神经退行性变与阿尔茨海默病(AD)的睡眠-觉醒失调有关,但 LC 完整性与昼夜节律休息-活动模式之间的关联尚不清楚。在这里,我们研究了在有和没有皮质 AD 神经病理学的老年人中,24 小时休息-活动节律、认知轨迹和尸检得出的 LC 完整性之间的关系。
这项回顾性研究利用了纵向临床病理 Rush 记忆和衰老项目参与者的多模态数据。从每年的活动记录仪记录中提取 24 小时休息-活动节律的碎片化(日内可变性)和稳定性(日间稳定性)指数,并从每年的认知评估中计算认知轨迹。在尸检时,通过色素减退来确定 LC 神经退行性变,评估皮质 AD 神经病理学。评估了共病病理(路易体、脑血管病病理学)的贡献。
在纳入研究样本的 388 例病例中(死亡时年龄为 92.1±5.9 岁;273 名女性),98 例(25.3%)显示 LC 色素减退,251 例(64.7%)显示皮质 AD 神经病理学。逻辑回归模型显示,在死亡前长达约 7.1 年的时间里,更高的休息-活动节律碎片化与尸检时 LC 神经退行性变的风险增加有关(比值比[OR]为 1.46,95%置信区间[CI]:1.16-1.84,p=0.004),尤其是在有皮质 AD 神经病理学的个体中(OR 为 1.56,CI:1.15-2.15,p=0.03),且与共病病理无关。此外,休息-活动节律碎片化的纵向增加部分介导了 LC 神经退行性变与认知下降之间的关联(估计值为-0.011,CI:-0.023--0.002,p=0.03)。
这些发现强调了 LC 是 AD 睡眠-觉醒失调的神经生物学相关物,并进一步强调了监测休息-活动模式对于提高高危个体检测的临床意义。