Silva-Rudberg Jason A, Salardini Elaheh, O'Dell Ryan S, Chen Ming-Kai, Ra Jocelyn, Georgelos Jamie K, Morehouse Mackenzie R, Melino Kaitlyn P, Varma Pradeep, Toyonaga Takuya, Nabulsi Nabeel B, Huang Yiyun, Carson Richard E, van Dyck Christopher H, Mecca Adam P
Alzheimer's Disease Research Unit (JAS-R, ES, RSO, JR, JKG, MRM, KPM, CHvD, APM), Yale University School of Medicine, New Haven, CT; Department of Psychiatry (JAS-R, ES, RSO, JR, JKG, MRM, KPM, CHvD, APM), Yale University School of Medicine, New Haven, CT.
Alzheimer's Disease Research Unit (JAS-R, ES, RSO, JR, JKG, MRM, KPM, CHvD, APM), Yale University School of Medicine, New Haven, CT; Department of Psychiatry (JAS-R, ES, RSO, JR, JKG, MRM, KPM, CHvD, APM), Yale University School of Medicine, New Haven, CT.
Am J Geriatr Psychiatry. 2024 Jan;32(1):17-28. doi: 10.1016/j.jagp.2023.08.002. Epub 2023 Aug 11.
Multimodal imaging techniques have furthered our understanding of how different aspects of Alzheimer's disease (AD) pathology relate to one another. Diffusion tensor imaging (DTI) measures such as mean diffusivity (MD) may be a surrogate measure of the changes in gray matter structure associated with AD. Positron emission tomography (PET) imaging of synaptic vesicle glycoprotein 2A (SV2A) has been used to quantify synaptic loss, which is the major pathological correlate of cognitive impairment in AD. In this study, we investigated the relationship between gray matter microstructure and synaptic density.
DTI was used to measure MD and [C]UCB-J PET to measure synaptic density in 33 amyloid-positive participants with AD and 17 amyloid-negative cognitively normal (CN) participants aged 50-83. Univariate regression analyses were used to assess the association between synaptic density and MD in both the AD and CN groups.
Hippocampal MD was inversely associated with hippocampal synaptic density in participants with AD (r = -0.55, p <0.001, df = 31) but not CN (r = 0.13, p = 0.62, df = 15). Exploratory analyses across other regions known to be affected in AD suggested widespread inverse associations between synaptic density and MD in the AD group.
In the setting of AD, an increase in gray matter MD is inversely associated with synaptic density. These co-occurring changes may suggest a link between synaptic loss and gray matter microstructural changes in AD. Imaging studies of gray matter microstructure and synaptic density may allow important insights into AD-related neuropathology.
多模态成像技术加深了我们对阿尔茨海默病(AD)病理学不同方面如何相互关联的理解。扩散张量成像(DTI)测量指标,如平均扩散率(MD),可能是与AD相关的灰质结构变化的替代指标。突触囊泡糖蛋白2A(SV2A)的正电子发射断层扫描(PET)成像已被用于量化突触丢失,这是AD认知障碍的主要病理相关因素。在本研究中,我们调查了灰质微观结构与突触密度之间的关系。
使用DTI测量33名年龄在50 - 83岁的淀粉样蛋白阳性AD参与者和17名淀粉样蛋白阴性认知正常(CN)参与者的MD,并使用[C]UCB - J PET测量突触密度。单变量回归分析用于评估AD组和CN组中突触密度与MD之间的关联。
AD参与者海马MD与海马突触密度呈负相关(r = -0.55,p <0.001,自由度 = 31),而CN参与者中无此相关性(r = 0.13,p = 0.62,自由度 = 15)。对AD中其他已知受影响区域的探索性分析表明,AD组中突触密度与MD之间存在广泛的负相关。
在AD背景下,灰质MD增加与突触密度呈负相关。这些同时出现的变化可能表明AD中突触丢失与灰质微观结构变化之间存在联系。对灰质微观结构和突触密度的成像研究可能有助于深入了解AD相关神经病理学。