Li Xinwei, Li Qiongling, Wang Xuetong, Li Deyu, Li Shuyu
School of Biological Science and Medical Engineering, Beihang University, Beijing, China.
Beijing Advanced Innovation Centre for Biomedical Engineering, Beihang University, Beijing, China.
Front Physiol. 2018 May 9;9:518. doi: 10.3389/fphys.2018.00518. eCollection 2018.
The hippocampus plays an important role in memory function relying on information interaction between distributed brain areas. The hippocampus can be divided into the anterior and posterior sections with different structure and function along its long axis. The aim of this study is to investigate the effects of normal aging on the structural covariance of the anterior hippocampus (aHPC) and the posterior hippocampus (pHPC). In this study, 240 healthy subjects aged 18-89 years were selected and subdivided into young (18-23 years), middle-aged (30-58 years), and older (61-89 years) groups. The aHPC and pHPC was divided based on the location of uncal apex in the MNI space. Then, the structural covariance networks were constructed by examining their covariance in gray matter volumes with other brain regions. Finally, the influence of age on the structural covariance of these hippocampal sections was explored. We found that the aHPC and pHPC had different structural covariance patterns, but both of them were associated with the medial temporal lobe and insula. Moreover, both increased and decreased covariances were found with the aHPC but only increased covariance was found with the pHPC with age ( < 0.05, family-wise error corrected). These decreased connections occurred within the default mode network, while the increased connectivity mainly occurred in other memory systems that differ from the hippocampus. This study reveals different age-related influence on the structural networks of the aHPC and pHPC, providing an essential insight into the mechanisms of the hippocampus in normal aging.
海马体在依赖分布式脑区之间信息交互的记忆功能中发挥着重要作用。海马体可沿其长轴分为结构和功能不同的前部和后部。本研究的目的是探讨正常衰老对海马体前部(aHPC)和后部(pHPC)结构协方差的影响。在本研究中,选取了240名年龄在18 - 89岁的健康受试者,并将其细分为青年组(18 - 23岁)、中年组(30 - 58岁)和老年组(61 - 89岁)。根据MNI空间中钩尖的位置划分aHPC和pHPC。然后,通过检查它们与其他脑区灰质体积的协方差来构建结构协方差网络。最后,探讨年龄对这些海马体节段结构协方差的影响。我们发现,aHPC和pHPC具有不同的结构协方差模式,但它们均与内侧颞叶和脑岛相关。此外,随着年龄增长,aHPC既有协方差增加的情况,也有协方差减少的情况,而pHPC只有协方差增加的情况(<0.05,经族系误差校正)。这些减少的连接发生在默认模式网络内,而增加的连接主要发生在与海马体不同的其他记忆系统中。本研究揭示了年龄对aHPC和pHPC结构网络的不同影响,为正常衰老过程中海马体的机制提供了重要见解。