Department of Biomedical Engineering, National University of Singapore, Singapore, Singapore.
The N.1 Institute for Health, National University of Singapore, Singapore, Singapore.
Hum Brain Mapp. 2021 Jun 15;42(9):2931-2940. doi: 10.1002/hbm.25414. Epub 2021 Mar 19.
This study is an observational study that takes the existing longitudinal data from Alzheimer's disease Neuroimaging Initiative to examine the spatial correlation map of hippocampal subfield atrophy with CSF biomarkers and cognitive decline in the course of AD. This study included 421 healthy controls (HC), 557 patients of stable mild cognitive impairment (s-MCI), 304 Alzheimer's Disease (AD) patients, and 241 subjects who converted to be AD from MCI (c-MCI), and 6,525 MRI scans in a period from 2004 to 2019. Our findings revealed that all the hippocampal subfields showed their accelerated atrophy rate from cognitively normal aging to stable MCI and AD. The presubiculum, dentate gyrus, and fimbria showed greater atrophy beyond the whole hippocampus in the HC, s-MCI, and AD groups and corresponded to a greater decline of memory and attention in the s-MCI group. Moreover, the higher atrophy rates of the subiculum and CA2/3, CA4 were also associated with a greater decline in attention in the s-MCI group. Interestingly, patients with c-MCI showed that the presubiculum atrophy was associated with CSF tau levels and corresponded to the onset age of AD and a decline in attention in patients with c-MCI. These spatial correlation findings of the hippocampus suggested that the hippocampal subfields may not be equally impacted by normal aging, MCI, and AD, and their atrophy was selectively associated with declines in specific cognitive domains. The presubiculum atrophy was highlighted as a surrogate marker for the AD prognosis along with tau pathology and attention decline.
本研究是一项观察性研究,利用阿尔茨海默病神经影像学倡议(Alzheimer's disease Neuroimaging Initiative)现有的纵向数据,研究海马亚区萎缩与脑脊液生物标志物及 AD 病程中认知下降的空间相关图。该研究纳入了 421 名健康对照者(HC)、557 名稳定轻度认知障碍(s-MCI)患者、304 名阿尔茨海默病(AD)患者和 241 名从 MCI 转化为 AD 的患者(c-MCI),以及 2004 年至 2019 年期间的 6525 份 MRI 扫描。我们的研究结果显示,所有海马亚区从认知正常老化到稳定 MCI 和 AD 都表现出加速萎缩率。在 HC、s-MCI 和 AD 组中,前下托、齿状回和卷边与整个海马相比表现出更大的萎缩,与 s-MCI 组记忆和注意力的更大下降相对应。此外,海马旁回和 CA2/3、CA4 的更高萎缩率也与 s-MCI 组注意力的更大下降有关。有趣的是,c-MCI 患者的前下托萎缩与 CSF tau 水平相关,与 AD 的发病年龄和 c-MCI 患者注意力下降相对应。这些海马的空间相关发现表明,海马亚区可能不会受到正常老化、MCI 和 AD 的同等影响,其萎缩与特定认知领域的下降选择性相关。前下托萎缩被强调为 AD 预后的替代标志物,与 tau 病理学和注意力下降有关。