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阿尔茨海默病和非阿尔茨海默病痴呆早期的神经精神症状,以及进展为严重痴呆的风险。

Neuropsychiatric symptoms in early stage of Alzheimer's and non-Alzheimer's dementia, and the risk of progression to severe dementia.

机构信息

Department of Psychiatry, Singapore General Hospital, Singapore.

Saw Swee Hock School of Public Health, National University of Singapore, Singapore.

出版信息

Age Ageing. 2021 Sep 11;50(5):1709-1718. doi: 10.1093/ageing/afab044.

Abstract

BACKGROUND

Neuropsychiatric symptoms (NPSs) in early dementia have been suggested to predict a higher risk of dementia progression. However, the literature is not yet clear whether the risk is similar across Alzheimer's dementia (AD) and non-Alzheimer's dementia (non-AD), as well as across different NPSs. This study examined the association between NPSs in early dementia and the risk of progression to severe dementia, specifically in AD and non-AD, as well as across various NPSs.

METHOD

This cohort study included 7,594 participants who were ≥65 years and had early dementia (global Clinical Dementia Rating [CDR] = 1). Participants completed Neuropsychiatric-Inventory-Questionnaire at baseline and were followed-up almost annually for progression to severe dementia (global CDR = 3) (median follow-up = 3.5 years; interquartile range = 2.1-5.9 years). Cox regression was used to examine progression risk, stratified by AD and non-AD.

RESULTS

The presence of NPSs was associated with risk of progression to severe dementia, but primarily in AD (HR 1.4, 95% confidence interval [CI]: 1.1-1.6) and not in non-AD (HR 0.9, 95% CI: 0.5-1.5). When comparing across various NPSs, seven NPSs in AD were associated with disease progression, and they were depression, anxiety, apathy, delusions, hallucinations, irritability and motor disturbance (HR 1.2-1.6). In contrast, only hallucinations and delusions were associated with disease progression in non-AD (HR 1.7-1.9).

CONCLUSIONS

NPSs in early dementia-especially among individuals with AD-can be useful prognostic markers of disease progression. They may inform discussion on advanced care planning and prompt clinical review to incorporate evidence-based interventions that may address disease progression.

摘要

背景

早期痴呆症患者的神经精神症状(NPS)已被认为可预测痴呆症进展的风险更高。然而,文献尚不清楚该风险在阿尔茨海默病(AD)和非阿尔茨海默病(非 AD)痴呆以及不同的 NPS 之间是否相似。本研究检查了早期痴呆症中 NPS 与进展为严重痴呆症(特别是 AD 和非 AD)以及各种 NPS 之间的风险之间的关联。

方法

这项队列研究纳入了 7594 名年龄≥65 岁且患有早期痴呆症(总体临床痴呆评定量表 [CDR] = 1)的患者。患者在基线时完成了神经精神问卷-问卷,并在近 1 年期间进行了随访,以评估进展为严重痴呆症(总体 CDR = 3)的情况(中位随访时间= 3.5 年;四分位间距 [IQR] = 2.1-5.9 年)。使用 Cox 回归分析来检查进展风险,风险分层为 AD 和非 AD。

结果

NPS 的存在与进展为严重痴呆症的风险相关,但主要与 AD(风险比 [HR] 1.4,95%置信区间 [CI]:1.1-1.6)相关,而与非 AD 无关(HR 0.9,95% CI:0.5-1.5)。在比较各种 NPS 时,AD 中的七种 NPS 与疾病进展相关,这些 NPS 是抑郁、焦虑、淡漠、妄想、幻觉、易怒和运动障碍(HR 1.2-1.6)。相比之下,只有幻觉和妄想与非 AD 中的疾病进展相关(HR 1.7-1.9)。

结论

早期痴呆症中的 NPS-尤其是在 AD 患者中-可以作为疾病进展的有用预后标志物。它们可以为高级护理计划的讨论提供信息,并促使进行临床审查,以纳入可能解决疾病进展的基于证据的干预措施。

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