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非优势顶叶位置随正常衰老而变化。

Uncal apex position varies with normal aging.

机构信息

Department of Psychology, Queen's University, Kingston, Ontario, Canada.

Centre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada.

出版信息

Hippocampus. 2020 Jul;30(7):724-732. doi: 10.1002/hipo.23196. Epub 2020 Feb 14.

Abstract

The uncal apex is an anatomical landmark frequently used for segmenting the hippocampus into its anterior and posterior segments, a necessary step for computing many measurements of its long axis. It functions well, as it is both local to the hippocampus and easy to identify. However, in spite of widespread use and definition in the EADC-ADNI Harmonized Hippocampal Protocol (HarP), how the uncal apex is influenced by gross hippocampal changes during normal aging has not been established, nor has the possible impact on measures of anterior hippocampus (aHPC) and posterior hippocampus (pHPC) volume. Here I drew upon three large data sets to describe and confirm these relationships, investigating them in one large data set and replicating my findings in the two others, evaluating a total of 4,434 hippocampi. I found the uncal apex fell in an increasingly more anterior position with increasing age. This age-related retraction of the uncus began after age 36, with the sharpest effects arising after age 60. This phenomenon exaggerates age-related aHPC volume decreases while simultaneously underestimating age-related pHPC volume decreases, a pattern I confirmed by juxtaposing uncal apex and MNI space-based landmarking. A hippocampally based reference frame was also rendered unstable by age-related shifts in the posterior extent of the hippocampus. Both the uncal apex and hippocampal reference frame should therefore be used with caution in aging research, or in research involving other demographic or disease factors known to evoke gross changes in the hippocampus. Instead, MNI coordinate-based heuristics may be appropriate for segmenting the hippocampus in study designs involving such factors. Apex-based segmentation is still attractive, however, in study designs where advanced age and atrophy are not used as regressors, including investigations into long-axis effects in healthy young adults. Progress toward localizing functional divisions within the hippocampus is needed to identify best practices for the field.

摘要

脑回尖是一个常用于将海马体分割为前、后段的解剖学标志,这是计算其长轴许多测量值的必要步骤。它的功能很好,因为它既位于海马体内部,又易于识别。然而,尽管在 EADC-ADNI 标准化海马体协议 (HarP) 中广泛使用和定义,脑回尖在正常衰老过程中如何受到海马体大体变化的影响尚未确定,也不知道它对前海马体 (aHPC) 和后海马体 (pHPC) 体积测量的可能影响。在这里,我利用三个大型数据集来描述和确认这些关系,在一个大型数据集中进行研究,并在另外两个数据集中复制我的发现,总共评估了 4434 个海马体。我发现脑回尖随着年龄的增长而越来越向前移动。这种与年龄相关的钩回退缩始于 36 岁以后,60 岁以后出现最明显的影响。这种现象夸大了与年龄相关的 aHPC 体积减少,同时低估了与年龄相关的 pHPC 体积减少,我通过将脑回尖和 MNI 空间的基于地标定位的方法进行对比来证实了这一模式。年龄相关的海马体后部延伸的变化也使基于海马体的参考框架不稳定。因此,在老龄化研究或涉及已知会引起海马体大体变化的其他人口统计学或疾病因素的研究中,应谨慎使用脑回尖和海马体参考框架。相反,对于涉及这些因素的研究设计,MNI 坐标基启发式可能更适合分割海马体。基于脑回尖的分割仍然具有吸引力,然而,在研究设计中,高级年龄和萎缩不作为回归因子使用,包括在健康年轻成年人中研究长轴效应的研究。需要确定该领域的最佳实践,以实现对海马体内部功能分区的本地化。

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