Geriatric Medicine, Centre for Public Health, School of Medicine, Dentistry & Biomedical Sciences, Whitla Medical Building, Queen's University Belfast, 97 Lisburn Road, Belfast BT9 7BL, United Kingdom.
Neurosci Lett. 2010 Oct 8;483(1):62-6. doi: 10.1016/j.neulet.2010.07.063. Epub 2010 Aug 1.
The apolipoprotein (APOE) epsilon4 allele is a genetic risk factor for the development of Alzheimer's disease (AD). It has also been associated with vascular dementia (VaD) in some but not all studies. Previous studies have examined the role of APOE in predicting performance on cognitive tests in both demented and non-demented populations. In cognitively intact individuals, statistically significant group differences between APOE epsilon4 carriers and non-carriers have been demonstrated for several cognitive domains. In AD studies of the impact of APOE epsilon4 on cognition have been conflicting while no previous study has assessed cognition and impact of APOE epsilon4 in VaD. In this study we investigated the impact of APOE epsilon4 on performance in neuropsychological tests including information processing speed in patients with mild-moderate AD and VaD. We incorporated both computerized and pen and paper tests to ensure a sensitive method of assessing cognition. 109 patients participated in the study (VaD=41, AD=68). Neurocognitive performance of 44 epsilon4 present AD patients was compared to 24 epsilon4absent patients and performance of 23 epsilon4 present VaD patients was compared to 18 epsilon4 absent patients. There was evidence that APOE epsilon4 conferred a risk of poorer cognitive functioning in both patient groups. In the AD group presence of epsilon4 conferred a negative impact on some measures of speed of information processing and immediate recall while in the VaD group epsilon4 present patients had evidence of poorer accuracy on tasks such as choice reaction time and spatial working memory. In AD and VaD groups epsilon4 present patients showed impairment in selective attention. These findings provide further support of the negative impact of the epsilon4 allele in cognition.
载脂蛋白(APOE)ε4 等位基因是阿尔茨海默病(AD)发展的遗传风险因素。在一些研究中,它也与血管性痴呆(VaD)有关,但并非所有研究都如此。以前的研究已经检查了 APOE 在预测痴呆和非痴呆人群认知测试表现中的作用。在认知正常的个体中,APOE ε4 携带者和非携带者在几个认知领域的统计学显著组间差异已经得到证明。在 AD 研究中,APOE ε4 对认知的影响存在冲突,而以前的研究尚未评估 VaD 中 APOE ε4 的认知和影响。在这项研究中,我们研究了 APOE ε4 对轻度至中度 AD 和 VaD 患者神经心理学测试中信息处理速度等表现的影响。我们结合了计算机化和纸笔测试,以确保评估认知的敏感方法。109 名患者参与了研究(VaD=41,AD=68)。比较了 44 名携带 APOE ε4 的 AD 患者和 24 名不携带 APOE ε4 的患者的神经认知表现,比较了 23 名携带 APOE ε4 的 VaD 患者和 18 名不携带 APOE ε4 的患者的神经认知表现。有证据表明,APOE ε4 使两组患者的认知功能更差的风险增加。在 AD 组中,ε4 的存在对某些信息处理速度和即时回忆的测量有负面影响,而在 VaD 组中,ε4 存在的患者在选择反应时间和空间工作记忆等任务上的准确性较差。在 AD 和 VaD 组中,ε4 存在的患者表现出选择性注意力受损。这些发现为ε4 等位基因对认知的负面影响提供了进一步的支持。