Abstract
The apolipoprotein (APOE) ɛ4 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 ɛ4 carriers and non-carriers have been demonstrated for several cognitive domains. In AD studies of the impact of APOE ɛ4 on cognition have been conflicting while no previous study has assessed cognition and impact of APOE ɛ4 in VaD. In this study we investigated the impact of APOE ɛ4 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 ɛ4 present AD patients was compared to 24 ɛ4absent patients and performance of 23 ɛ4 present VaD patients was compared to 18 ɛ4 absent patients. There was evidence that APOE ɛ4 conferred a risk of poorer cognitive functioning in both patient groups. In the AD group presence of ɛ4 conferred a negative impact on some measures of speed of information processing and immediate recall while in the VaD group ɛ4 present patients had evidence of poorer accuracy on tasks such as choice reaction time and spatial working memory. In AD and VaD groups ɛ4 present patients showed impairment in selective attention. These findings provide further support of the negative impact of the ɛ4 allele in cognition.
Published Version (
Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
