轻度行为障碍、睡眠障碍与痴呆症进展之间的纵向联系。

IF 2.8 Q2 NEUROSCIENCES Journal of Alzheimer's disease reports Pub Date : 2023-12-06 eCollection Date: 2023-01-01 DOI:10.3233/ADR-230086
Dinithi Mudalige, Dylan X Guan, Maryam Ghahremani, Zahinoor Ismail
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引用次数: 0

摘要

背景:临床指南建议将轻度行为障碍(MBI)和睡眠障碍(SD)等非认知标记纳入痴呆症筛查,以提高发现率:我们研究了 MBI、SD 与痴呆症事件之间的纵向关联:参与者数据来自美国国家阿尔茨海默氏症协调中心。MBI通过神经精神量表问卷(NPI-Q)得出,采用的是一种已公布的算法。SD通过NPI-Q夜间行为项目确定。利用MBI、SD和认知诊断的时间依赖变量进行Cox比例危险回归,以建立基线1)MBI和事件SD(n = 11,277);2)SD和事件MBI(n = 10,535);3)并发SD的MBI和事件痴呆(n = 13,544);4)不并发SD的MBI和事件痴呆(n = 11,921)之间的关联模型。模型根据首次就诊的年龄、性别、教育程度、认知诊断、种族进行了调整,并使用本杰明-霍奇伯格方法进行了多重比较:基线时患有 MBI 的老年人的 SD 患病率是未患有 MBI 的老年人的 3.1 倍(95% CI:2.8-3.3)。基线值为 SD 的老年人患 MBI 的比例是未患 SD 的老年人的 1.5 倍(95% CI:1.3-1.8)。同时患有MBI和SD的老年人患痴呆症的比例是单独患有SD的老年人的2.2倍(95% CI:1.9-2.6):结论:MBI和SD之间存在双向关系。结论:MBI和SD之间存在双向关系,当SD与MBI同时存在时,患有SD的老年人患痴呆症的比例更高。未来的研究应探索这些关系的内在机制,同时评估MBI和SD可能会改善痴呆症筛查。
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Longitudinal Associations Between Mild Behavioral Impairment, Sleep Disturbance, and Progression to Dementia.

Background: Clinical guidelines recommend incorporating non-cognitive markers like mild behavioral impairment (MBI) and sleep disturbance (SD) into dementia screening to improve detection.

Objective: We investigated the longitudinal associations between MBI, SD, and incident dementia.

Methods: Participant data were from the National Alzheimer's Coordinating Center in the United States. MBI was derived from the Neuropsychiatric Inventory Questionnaire (NPI-Q) using a published algorithm. SD was determined using the NPI-Q nighttime behaviors item. Cox proportional hazard regressions with time-dependant variables for MBI, SD, and cognitive diagnosis were used to model associations between baseline 1) MBI and incident SD (n = 11,277); 2) SD and incident MBI (n = 10,535); 3) MBI with concurrent SD and incident dementia (n = 13,544); and 4) MBI without concurrent SD and incident dementia (n = 11,921). Models were adjusted for first-visit age, sex, education, cognitive diagnosis, race, and for multiple comparisons using the Benjamini-Hochberg method.

Results: The rate of developing SD was 3.1-fold higher in older adults with MBI at baseline compared to those without MBI (95% CI: 2.8-3.3). The rate of developing MBI was 1.5-fold higher in older adults with baseline SD than those without SD (95% CI: 1.3-1.8). The rate of developing dementia was 2.2-fold greater in older adults with both MBI and SD, as opposed to SD alone (95% CI:1.9-2.6).

Conclusions: There is a bidirectional relationship between MBI and SD. Older adults with SD develop dementia at higher rates when co-occurring with MBI. Future studies should explore the mechanisms underlying these relationships, and dementia screening may be improved by assessing for both MBI and SD.

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