Alexander Gene E, Chen Kewei, Aschenbrenner Melaney, Merkley Tricia L, Santerre-Lemmon Laura E, Shamy Jul Lea, Skaggs William E, Buonocore Michael H, Rapp Peter R, Barnes Carol A
Department of Psychology, Arizona State University, Phoenix, Arizona 85287-1104, USA.
J Neurosci. 2008 Mar 12;28(11):2710-8. doi: 10.1523/JNEUROSCI.1852-07.2008.
Human structural neuroimaging studies have supported the preferential effects of healthy aging on frontal cortex, but reductions in other brain regions have also been observed. We investigated the regional network pattern of gray matter using magnetic resonance imaging (MRI) in young adult and old rhesus macaques (RMs) to evaluate age effects throughout the brain in a nonhuman primate model of healthy aging in which the full complement of Alzheimer's disease (AD) pathology does not occur. Volumetric T1 MRI scans were spatially normalized and segmented for gray matter using statistical parametric mapping (SPM2) voxel-based morphometry. Multivariate network analysis using the scaled subprofile model identified a linear combination of two gray matter patterns that distinguished the young from old RMs. The combined pattern included reductions in bilateral dorsolateral and ventrolateral prefrontal and orbitofrontal and superior temporal sulcal regions with areas of relative preservation in vicinities of the cerebellum, globus pallidus, visual cortex, and parietal cortex in old compared with young RMs. Higher expression of this age-related gray matter pattern was associated with poorer performance in working memory. In the RM model of healthy aging, the major regionally distributed effects of advanced age on the brain involve reductions in prefrontal regions and in the vicinity of the superior temporal sulcus. The age-related differences in gray matter reflect the effects of healthy aging that cannot be attributed to AD pathology, providing support for the targeted effects of aging on the integrity of frontal lobe regions and selective temporal lobe areas and their associated cognitive functions.
人类结构神经影像学研究支持健康衰老对额叶皮质有优先影响,但也观察到其他脑区有萎缩。我们使用磁共振成像(MRI)研究了年轻成年和老年恒河猴(RMs)的灰质区域网络模式,以评估在未出现阿尔茨海默病(AD)全部病理特征的健康衰老非人灵长类动物模型中,年龄对全脑的影响。使用基于体素的形态学分析软件(SPM2)对容积T1 MRI扫描进行空间标准化和灰质分割。使用缩放子轮廓模型进行多变量网络分析,确定了区分年轻和老年RMs的两种灰质模式的线性组合。与年轻RMs相比,老年RMs的组合模式包括双侧背外侧和腹外侧前额叶、眶额叶和颞上沟区域萎缩,而小脑、苍白球、视觉皮质和顶叶皮质附近区域相对保留。这种与年龄相关的灰质模式表达越高,工作记忆表现越差。在健康衰老的RMs模型中,高龄对大脑的主要区域分布影响包括前额叶区域和颞上沟附近区域萎缩。灰质中与年龄相关的差异反映了健康衰老的影响,而非AD病理特征所致,这为衰老对额叶区域和选择性颞叶区域完整性及其相关认知功能的靶向作用提供了支持。