Negash Selam, Greenwood Pamela M, Sunderland Trey, Parasuraman Raja, Geda Yonas E, Knopman David S, Boeve Bradley F, Ivnik Robert J, Petersen Ronald C, Smith Glenn E
Department of Neurology, Mayo Clinic, USA.
Neuropsychology. 2009 Jan;23(1):81-9. doi: 10.1037/a0014014.
Although it is established that apolipoprotein E (APOE) e4 allele increases the risk of Alzheimer's disease (AD), epidemiological studies indicate that genetic risk decreases late in life. This raises the question of whether the effects of APOE on cognition that are seen in midlife arise from a cognitive phenotype of APOE or from the presence of early AD in some APOE-e4 carriers. The authors addressed this question by comparing the cognitive consequences of variation in the APOE gene between individuals over the age of 80 (old-old) and middle-aged and young-old individuals. A spatially cued discrimination paradigm--previously shown to be sensitive to AD and to APOE genotype--required a speeded categorization of a target letter following cues that were valid, invalid, or neutral in predicting target location. Results revealed greater costs of invalid cues in the APOE-e4 carriers of middle-aged and young-old, but not old-old, groups. The dissipation of the APOE effect in old-old individuals at lower risk of AD suggests that visuospatial attention impairments seen as early as midlife in APOE-e4 carriers may be a preclinical marker of AD.
尽管已确定载脂蛋白E(APOE)e4等位基因会增加患阿尔茨海默病(AD)的风险,但流行病学研究表明,遗传风险在生命后期会降低。这就引出了一个问题,即APOE在中年时对认知的影响是源于APOE的认知表型,还是源于一些APOE-e4携带者中存在早期AD。作者通过比较80岁以上(高龄)个体与中年和年轻老年人之间APOE基因变异的认知后果来解决这个问题。一种空间线索辨别范式——先前已证明对AD和APOE基因型敏感——要求在预测目标位置有效、无效或中性的线索后,对目标字母进行快速分类。结果显示,在中年和年轻老年组的APOE-e4携带者中,无效线索的代价更大,但在高龄组中并非如此。在AD风险较低的高龄个体中APOE效应的消失表明,APOE-e4携带者早在中年时出现的视觉空间注意力损害可能是AD的临床前标志物。