Li Janice X, Nguyen Hannah L, Qian Tianchen, Woodworth Davis C, Sajjadi S Ahmad
Department of Neurology, University of California, Irvine, CA, USA.
Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, CA, USA.
Aging Brain. 2023 Aug 12;4:100092. doi: 10.1016/j.nbas.2023.100092. eCollection 2023.
Hippocampal sclerosis of aging (HS-A) is a common degenerative neuropathology in older individuals and is associated with dementia. HS-A is characterized by disproportionate hippocampal atrophy at autopsy but cannot be diagnosed during life. Therefore, little is known about the onset and progression of hippocampal atrophy in individuals with HS-A. To better understand the onset and progression of hippocampal atrophy in HS-A, we examined longitudinal hippocampal atrophy using serial MRI in participants with HS-A at autopsy (HS-A+, n = 8) compared to participants with limbic-predominant age-related TDP-43 encephalopathy neuropathological change (LATE-NC) without HS-A (n = 13), Alzheimer's disease neuropathologic change (ADNC) without HS-A or LATE-NC (n = 16), and those without these pathologies (n = 7). We found that participants with HS-A had lower hippocampal volumes compared to the other groups, and this atrophy preceded the onset of dementia. There was also some evidence that rates of hippocampal volume loss were slightly slower in those with HS-A. Together, these results suggest that the disproportionate hippocampal atrophy seen in HS-A may begin early prior to dementia.
衰老性海马硬化(HS-A)是老年人常见的一种退行性神经病理学表现,与痴呆症相关。HS-A的特征是尸检时海马体出现不成比例的萎缩,但生前无法诊断。因此,对于患有HS-A的个体,海马萎缩的起始和进展情况知之甚少。为了更好地了解HS-A中海马萎缩的起始和进展,我们对尸检时患有HS-A的参与者(HS-A+,n = 8)与没有HS-A的边缘性为主的年龄相关性TDP-43脑病神经病理学改变(LATE-NC)参与者(n = 13)、没有HS-A或LATE-NC的阿尔茨海默病神经病理学改变(ADNC)参与者(n = 16)以及没有这些病理学改变的参与者(n = 7),使用系列磁共振成像检查了海马的纵向萎缩情况。我们发现,与其他组相比,患有HS-A的参与者海马体积较小,且这种萎缩在痴呆症发作之前就已出现。也有一些证据表明,HS-A患者的海马体积丢失率略慢。总之,这些结果表明,HS-A中出现的不成比例的海马萎缩可能在痴呆症之前就已早期开始。