Chang Ya-Ting, Huang Chi-Wei, Chen Nai-Ching, Lin Kun-Ju, Huang Shu-Hua, Chang Wen-Neng, Hsu Shih-Wei, Hsu Che-Wei, Chen Hsiu-Hui, Chang Chiung-Chih
Departments of Neurology, Cognition and Aging Center, Kaohsiung Chang Gung Memorial Hospital, Chang Gung University College of Medicine Kaohsiung, Taiwan.
Department of Nuclear Medicine and Center for Advanced Molecular Imaging and Translation, Chang Gung Memorial Hospital Taoyuan, Taiwan.
Front Aging Neurosci. 2016 Jun 17;8:145. doi: 10.3389/fnagi.2016.00145. eCollection 2016.
Neuronal activity during face matching shows co-activation of the fusiform gyrus (FG) and areas along the ventral visual network. To elucidate the mechanisms related to the facial discrimination deficits in Alzheimer's disease (AD), the study evaluates the relationships between β-amyloid (Aβ) load and gray matter (GM) atrophy within the ventral visual network.
Comprehensive cognitive assessments and GM volumetry using 3-dimentional T1-weighted images and AV-45 positron emission tomography (PET) were studied in 44 patients with AD. We used AV-45 PET to measure regional Aβ to analyze the correlations between the regional neocortical AV-45 retention and atrophy in patients with AD.
FG volume was positively correlated with the para-hippocampus (β = 0.565, P < 0.001), posterior cingulate cortex (PCC; β = 0.402, P < 0.001), and hippocampus volumes (β = 0.209, P = 0.044). After carefully confounded all possible factors simultaneously, the hippocampus standardized uptake value (SUV) ratio was independently associated with FG volume (β = -0.151, P = 0.017). Furthermore, volumes of the hippocampus (r = 0.473, P = 0.003), para-hippocampus (r = 0.515, P = 0.001), and FG (r = 0.383, P = 0.018) were associated with Benton's facial recognition test (BFRT).
In conclusion, our study indicated that amyloid burden within the hippocampus might contribute to FG cortical hub GM atrophy. While the face matching task scores were related to the FG, hippocampus, and para-hippocampus volumes, concordant changes of the aforementioned three structures suggested the importance of the three ventral visual network hubs in AD.
面部匹配过程中的神经元活动显示梭状回(FG)和腹侧视觉网络沿线区域共同激活。为阐明阿尔茨海默病(AD)中面部识别缺陷的相关机制,本研究评估了腹侧视觉网络内β-淀粉样蛋白(Aβ)负荷与灰质(GM)萎缩之间的关系。
对44例AD患者进行了综合认知评估,并使用三维T1加权图像和AV-45正电子发射断层扫描(PET)进行GM体积测量。我们使用AV-45 PET测量区域Aβ,以分析AD患者区域新皮质AV-45滞留与萎缩之间的相关性。
FG体积与海马旁回(β = 0.565,P < 0.001)、后扣带回皮质(PCC;β = 0.402,P < 0.001)和海马体积(β = 0.209,P = 0.044)呈正相关。在同时仔细混淆所有可能因素后,海马标准化摄取值(SUV)比率与FG体积独立相关(β = -0.151,P = 0.017)。此外,海马(r = 0.473,P = 0.003)、海马旁回(r = 0.515,P = 0.001)和FG(r = 0.383,P = 0.018)的体积与本顿面部识别测试(BFRT)相关。
总之,我们的研究表明海马内的淀粉样蛋白负荷可能导致FG皮质枢纽GM萎缩。虽然面部匹配任务得分与FG、海马和海马旁回体积有关,但上述三个结构的一致变化表明这三个腹侧视觉网络枢纽在AD中的重要性。