Luo Caimei, Li Mengchun, Qin Ruomeng, Chen Haifeng, Yang Dan, Huang Lili, Liu Renyuan, Xu Yun, Bai Feng, Zhao Hui
Department of Neurology, Nanjing Drum Tower Hospital, Nanjing University Medical School, Nanjing, China.
Jiangsu Key Laboratory for Molecular Medicine, Nanjing University Medical School, Nanjing, China.
Front Aging Neurosci. 2020 Jan 28;11:378. doi: 10.3389/fnagi.2019.00378. eCollection 2019.
: Subjective cognitive decline (SCD) is considered a preclinical state of Alzheimer's disease (AD) and may represent a more advanced preclinical status than amnestic mild cognitive impairment (aMCI). Our aim was to explore changes in the white matter (WM) microstructure and their correlation with cognitive function in these AD-spectrum patients. : Diffusion tensor images from 43 individuals with normal cognition (NC), 38 SCD patients, and 36 aMCI patients were compared using an atlas-based segmentation strategy. The correlation between diffusion parameters and cognitive function was further analyzed. : The anatomical pattern of WM impairment was generally similar between SCD and aMCI patients. However, aMCI patients showed significantly lower fractional anisotropy (i.e., corpus callosum forceps major and forceps minor) and increased mean diffusivity [i.e., bilateral anterior thalamic radiation (ATR), left corticospinal tract (CST), forceps minor, left cingulum (cingulate gyrus), left cingulum hippocampus, and left inferior fronto-occipital fasciculus (IFO)] in some tracts than did SCD subjects, indicating a disruption in WM microstructural integrity in the aMCI. Individuals with microstructural disruption in forceps minor, left cingulum (cingulate gyrus), and left cingulum hippocampus tracts performed worse in general cognition and memory function tests, as indicated by line regression analysis. : SCD individuals had extensive WM microstructural damage in a pattern similar to that seen in aMCI, although presenting a cognitive performance comparable with that of cognitively healthy individuals. Our results suggest that WM integrity might precede objectively measurable memory decline and may be a potential early biomarker for AD.
主观认知下降(SCD)被认为是阿尔茨海默病(AD)的临床前状态,可能代表比遗忘型轻度认知障碍(aMCI)更晚期的临床前状态。我们的目的是探讨这些AD谱系患者白质(WM)微观结构的变化及其与认知功能的相关性。
使用基于图谱的分割策略比较了43名认知正常(NC)个体、38名SCD患者和36名aMCI患者的扩散张量图像。进一步分析了扩散参数与认知功能之间的相关性。
SCD患者和aMCI患者的WM损伤解剖模式总体相似。然而,aMCI患者在某些脑区的分数各向异性显著降低(即胼胝体主要钳和次要钳),平均扩散率增加[即双侧丘脑前辐射(ATR)、左侧皮质脊髓束(CST)、次要钳、左侧扣带(扣带回)、左侧扣带海马和左侧额枕下束(IFO)],表明aMCI患者的WM微观结构完整性受到破坏。线性回归分析表明,次要钳、左侧扣带(扣带回)和左侧扣带海马脑区微观结构破坏的个体在一般认知和记忆功能测试中表现较差。
SCD个体存在广泛的WM微观结构损伤,其模式与aMCI相似,尽管其认知表现与认知健康个体相当。我们的结果表明,WM完整性可能先于客观可测量的记忆下降,可能是AD的潜在早期生物标志物。