Wattmo Carina, Minthon Lennart, Wallin Åsa K
Clinical Memory Research Unit, Department of Clinical Sciences, Malmö, Lund University, SE-205 02, Malmö, Sweden.
Alzheimers Res Ther. 2016 Feb 17;8:7. doi: 10.1186/s13195-016-0174-1.
There is an increasing interest in cognitive and functional outcomes in the respective stages of Alzheimer's disease (AD) and in novel therapies particularly for the milder phases of AD. Our aim was to describe and compare various aspects of disease progression in patients with mild versus moderate AD in routine clinical practice of cholinesterase inhibitor (ChEI) therapy.
This 3-year, prospective, observational, multicentre study included 1021 participants. Of these, 734 had mild AD (Mini-Mental State Examination (MMSE) score, 20-26) and 287 had moderate AD (MMSE score, 10-19) at the start of ChEI treatment. At baseline and every 6 months, patients were assessed using cognitive, global, instrumental and basic activities of daily living (ADL) scales. Potential predictors of deterioration in moderate AD were analysed using mixed-effects models.
The change from baseline between participants with mild and moderate stages of AD after 3 years of ChEI therapy differed significantly on the Alzheimer's Disease Assessment Scale-cognitive subscale (ADAS-cog) and basic ADL, but not using the MMSE and instrumental ADL scales. Protective independent factors for better cognitive long-term outcome in the group with moderate AD were older age, higher instrumental ADL ability, no antipsychotics, usage of non-steroidal anti-inflammatory drugs/acetylsalicylic acid, living with family member, lower education and a higher mean dose of ChEI. Apolipoprotein E genotype did not influence the rates of disease progression or the longitudinal outcomes. Prediction models were provided for moderate AD.
More sensitive cognitive measures, such as the ADAS-cog scale, are required to detect a possibly faster deterioration among the participants with moderate AD. This study highlighted the clinical importance of instrumental ADL evaluations in patients at a mild stage of AD, and the importance of optimizing the ChEI dose even for individuals with moderate AD. Solitary living was a risk factor for faster cognitive decline, and probably expanded the need for formal care in the group with moderate AD. The patients with more advanced AD and presumably more pronounced neuroinflammation might have additional cognitive benefits from longer-term treatment with anti-inflammatory drugs.
人们对阿尔茨海默病(AD)各阶段的认知和功能结局以及新型疗法,尤其是针对AD较轻阶段的疗法越来越感兴趣。我们的目的是在胆碱酯酶抑制剂(ChEI)治疗的常规临床实践中,描述和比较轻度与中度AD患者疾病进展的各个方面。
这项为期3年的前瞻性观察性多中心研究纳入了1021名参与者。其中,734例在ChEI治疗开始时患有轻度AD(简易精神状态检查表(MMSE)评分,20 - 26),287例患有中度AD(MMSE评分,10 - 19)。在基线和每6个月时,使用认知、整体、工具性和日常生活基本活动(ADL)量表对患者进行评估。使用混合效应模型分析中度AD病情恶化的潜在预测因素。
ChEI治疗3年后,轻度和中度AD患者从基线开始的变化在阿尔茨海默病评估量表认知子量表(ADAS - cog)和基本ADL方面有显著差异,但在MMSE和工具性ADL量表方面无显著差异。中度AD组认知长期结局较好的保护性独立因素包括年龄较大、工具性ADL能力较高、未使用抗精神病药物、使用非甾体抗炎药/阿司匹林、与家庭成员同住、教育程度较低以及ChEI平均剂量较高。载脂蛋白E基因型不影响疾病进展速度或纵向结局。提供了中度AD的预测模型。
需要更敏感的认知测量方法,如ADAS - cog量表,以检测中度AD参与者中可能更快的病情恶化。本研究强调了工具性ADL评估在轻度AD患者中的临床重要性,以及即使对于中度AD患者优化ChEI剂量的重要性。独居是认知衰退加快的一个危险因素,可能增加了中度AD组对正规护理的需求。AD进展更严重且可能神经炎症更明显的患者可能从长期使用抗炎药物治疗中获得额外的认知益处。