Department of Psychiatry, Singapore General Hospital, Singapore.
Saw Swee Hock School of Public Health, National University of Singapore, Singapore.
Age Ageing. 2021 Sep 11;50(5):1709-1718. doi: 10.1093/ageing/afab044.
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.
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.
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).
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.
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。
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。
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)。
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。