David Geffen School of Medicine at UCLA, Center for Cognitive Neurosciences, Semel Institute, Los Angeles, CA 90095, USA.
Neuroimage. 2010 Oct 15;53(1):37-43. doi: 10.1016/j.neuroimage.2010.06.009. Epub 2010 Jun 10.
People with the apolipoprotein-Eepsilon4 (APOE-4) genetic risk for Alzheimer's disease show morphologic differences in medial temporal lobe regions when compared to non-carriers of the allele. Using a high-resolution MRI and cortical unfolding approach, our aim was to determine the rate of cortical thinning among medial temporal lobe subregions over the course of 2 years. We hypothesized that APOE-4 genetic risk would contribute to longitudinal cortical thickness change in the subiculum and entorhinal cortex, regions preferentially susceptible to Alzheimer's disease related pathology. Thirty-two cognitively intact subjects, mean age 61 years, 16 APOE-4 carriers, 16 non-carriers, underwent baseline and follow-up MRI scans. Over this relatively brief interval, we found significantly greater cortical thinning in the subiculum and entorhinal cortex of APOE-4 carriers when compared to non-carriers of the allele. Average cortical thinning across all medial temporal lobe subregions combined was also significantly greater for APOE-4 carriers. This finding is consistent with the hypothesis that carrying the APOE-4 allele renders subjects at a higher risk for developing Alzheimer's disease.
与不携带该等位基因的人相比,载脂蛋白 E 基因型为 epsilon4(APOE-4)的阿尔茨海默病高危人群的内侧颞叶区域存在形态学差异。本研究采用高分辨率 MRI 和皮质展开方法,旨在确定在 2 年内内侧颞叶亚区的皮质变薄率。我们假设 APOE-4 遗传风险会导致内侧颞叶亚区,特别是易受阿尔茨海默病相关病理影响的海马和内嗅皮层的纵向皮质厚度变化。32 名认知正常的受试者,平均年龄 61 岁,16 名 APOE-4 携带者,16 名非携带者,进行了基线和随访 MRI 扫描。在这段相对较短的时间内,我们发现与非携带者相比,APOE-4 携带者的海马和内嗅皮层的皮质变薄更为显著。APOE-4 携带者的所有内侧颞叶亚区的平均皮质变薄也明显更大。这一发现与携带 APOE-4 等位基因的个体患阿尔茨海默病的风险更高的假设一致。