Memory Unit, Department of Neurology, Hospital de Cruces, Baracaldo, Vizcaya, Spain.
Curr Alzheimer Res. 2013 Jan;10(1):86-94. doi: 10.2174/1567205011310010012.
Neuropsychiatric symptoms (NPS) are common in mild cognitive impairment (MCI) but its role as a predictive factor for the progression to dementia is still not clear. The objective of this study is to identify NPS that predict the progression from amnestic MCI (a-MCI) to dementia using an easy to administer screening tool for NPS.
132 patients with a-MCI were assessed for NPS by the Neuropsychiatric Inventory (NPI) and followed to detect progression to dementia.
The mean follow-up time was 3.5±2.9 years and rate of progression to dementia 28.8%. Two items of NPI were found to be independent risk factors for progression, nighttime behavioural disturbance (hazard ratio(HR)=2.2, 95%CI=1.10-4.43), anxiety (HR=2.5, 95%CI=1.01-6.20) and apathy (HR=2.2, 95%CI=1.003-4.820). The risk of progression increased with higher score on NPI (HR=1.046 per point, 95%CI=1.019- 1.073), and with a higher number of items of NPI affected (HR=3.6 per item, 95%CI=2.0-6.4). Faster progression to dementia was observed in patients with either nighttime behavioural disturbance, apathy or anxiety (4.6 vs. 8.3 years, 5.3 vs. 8.4 years and 3.0 vs. 7.7 years respectively, p < 0.01) as well as in those with a higher number of items affected (no items = 9.2 years, 1-3 items = 6.6 years and > 3 items = 2.9 years, p < 0.001).
Assessing a broad spectrum of NPS can help identify patients with a-MCI presenting a higher risk for progression to dementia. This can be useful to select patients for closer follow-up, clinical trials and future therapeutic interventions.
神经精神症状(NPS)在轻度认知障碍(MCI)中很常见,但它作为向痴呆进展的预测因素尚不清楚。本研究的目的是使用一种易于管理的 NPS 筛查工具,确定可预测从遗忘型 MCI(a-MCI)进展为痴呆的 NPS。
对 132 名 a-MCI 患者进行神经精神病学问卷(NPI)评估,并进行随访以检测向痴呆的进展。
平均随访时间为 3.5±2.9 年,进展为痴呆的比例为 28.8%。有两项 NPI 项目被发现是进展的独立危险因素,夜间行为障碍(危险比(HR)=2.2,95%可信区间(CI)=1.10-4.43)、焦虑(HR=2.5,95%CI=1.01-6.20)和淡漠(HR=2.2,95%CI=1.003-4.820)。NPI 评分越高(HR=每增加 1 分 1.046,95%CI=1.019-1.073),受影响的 NPI 项目越多(HR=每增加 1 项 3.6,95%CI=2.0-6.4),进展的风险就越高。夜间行为障碍、淡漠或焦虑的患者向痴呆进展更快(4.6 与 8.3 年,5.3 与 8.4 年和 3.0 与 7.7 年,p<0.01),受影响的项目数也更多(无项目=9.2 年,1-3 个项目=6.6 年,>3 个项目=2.9 年,p<0.001)。
评估广泛的 NPS 可以帮助识别具有更高向痴呆进展风险的 a-MCI 患者。这对于选择需要更密切随访、临床试验和未来治疗干预的患者很有用。