Zebrowitz Leslie, Ward Noreen, Boshyan Jasmine, Gutchess Angela, Hadjikhani Nouchine
Department of Psychology, Brandeis University, Waltham, MA 02453, USA.
MGH/HST Athinoula A. Martinos Center for Biomedical Imaging, Harvard University, Boston, MA 02129 USA.
Brain Res. 2016 Aug 1;1644:22-31. doi: 10.1016/j.brainres.2016.05.007. Epub 2016 May 6.
We used multimodal brain imaging to examine possible mediators of age-related neural dedifferentiation (less specific neural activation) to different categories of stimuli that had been shown in previous research. Specifically, we examined resting blood flow and brain activation in areas involved in object, place and face perception. We observed lower activation, specificity, and resting blood flow for older adults (OA) than younger adults (YA) in the fusiform face area (FFA) but not in the other regions of interest. Mediation analyses further revealed that FFA resting state blood flow mediated age differences in FFA specificity, whereas age differences in visual and cognitive function and cortical thickness did not. Whole brain analyses also revealed more activated voxels for all categories in OA, as well as more frontal activation for faces but not for the other categories in OA than YA. Less FFA specificity coupled with more frontal activation when passively viewing faces suggest that OA have more difficulty recruiting specialized face processing mechanisms, and the lower FFA metabolic activity even when faces are not being processed suggests an OA deficiency in the neural substrate underlying face processing. Our data point to a detuning of face-selective mechanisms in older adults.
我们使用多模态脑成像技术来研究与年龄相关的神经去分化(神经激活特异性降低)的潜在介导因素,这些因素与先前研究中已显示的不同类别刺激有关。具体而言,我们研究了参与物体、地点和面部感知区域的静息血流和脑激活情况。我们观察到,与年轻人(YA)相比,老年人(OA)在梭状回面部区(FFA)的激活、特异性和静息血流较低,但在其他感兴趣区域则不然。中介分析进一步表明,FFA静息状态血流介导了FFA特异性的年龄差异,而视觉和认知功能以及皮质厚度的年龄差异则没有。全脑分析还显示,在OA中,所有类别的体素激活更多,并且与YA相比,OA在面部刺激时额叶激活更多,但在其他类别刺激时则不然。在被动观看面部时,FFA特异性降低且额叶激活增加,这表明OA在招募专门的面部处理机制方面存在更多困难,并且即使在不处理面部时FFA代谢活动较低,这表明OA在面部处理的神经基础方面存在缺陷。我们的数据表明老年人面部选择性机制失调。