Kreuzer Annika, Sauerbeck Julia, Scheifele Maximilian, Stockbauer Anna, Schönecker Sonja, Prix Catharina, Wlasich Elisabeth, Loosli Sandra V, M Kazmierczak Philipp, Unterrainer Marcus, Catak Cihan, Janowitz Daniel, Pogarell Oliver, Palleis Carla, Perneczky Robert, Albert Nathalie L, Bartenstein Peter, Danek Adrian, Buerger Katharina, Levin Johannes, Zwergal Andreas, Rominger Axel, Brendel Matthias, Beyer Leonie
Department of Nuclear Medicine, University Hospital, Ludwig-Maximilians-University Munich, Munich, Germany.
Department of Neurology, University Hospital, Ludwig-Maximilians-University, Munich, Germany.
Front Aging Neurosci. 2021 Feb 2;13:611595. doi: 10.3389/fnagi.2021.611595. eCollection 2021.
: Asymmetric disease characteristics on neuroimaging are common in structural and functional imaging of neurodegenerative diseases, particularly in Alzheimer's disease (AD). However, a standardized clinical evaluation of asymmetric neuronal degeneration and its impact on clinical findings has only sporadically been investigated for F-18-fluorodeoxyglucose positron emission tomography (F-18-FDG-PET). This study aimed to evaluate the impact of lateralized neuronal degeneration on the detection of AD by detailed clinical testing. Furthermore, we compared associations between clinical evaluation and lateralized neuronal degeneration between FDG-PET hypometabolism and hippocampal atrophy. Finally, we investigated if specific subtests show associations with lateralized neuronal degeneration. : One-hundred and forty-six patients with a clinical diagnosis of AD (age 71 ± 8) were investigated by FDG-PET and the "Consortium to Establish a Registry for Alzheimer's disease" (CERAD) test battery. For assessment of neuronal degeneration, FDG-PET hypometabolism in brain regions typically affected in AD were graded by visual (3D-surface projections) and semiquantitative analysis. Asymmetry of the hippocampus (left-right) in magnetic resonance tomography (MRI) was rated visually by the Scheltens scale. Measures of asymmetry were calculated to quantify lateralized neuronal degeneration and asymmetry scores were subsequently correlated with CERAD. : Asymmetry with left-dominant neuronal degeneration to FDG-PET was an independent predictor of cognitive impairment (visual: = -0.288, < 0.001; semiquantitative: = -0.451, < 0.001) when controlled for age, gender, years of education and total burden of neuronal degeneration, whereas hippocampal asymmetry to MRI was not ( = -0.034; = 0.731). Direct comparison of CERAD-PET associations in cases with right- and left-lateralized neuronal degeneration estimated a detection gap of 2.7 years for right-lateralized cases. Left-hemispheric neuronal degeneration was significantly associated with the total CERAD score and multiple subscores, whereas only MMSE (semiquantitative: = 0.429, < 0.001) and constructional praxis (semiquantitative: = 0.292, = 0.008) showed significant associations with right-hemispheric neuronal degeneration. : Asymmetry of deteriorated cerebral glucose metabolism has a significant impact on the coupling between neuronal degeneration and cognitive function. Right dominant neuronal degeneration shows a delayed detection by global CERAD testing and requires evaluation of specific subdomains of cognitive testing.
神经影像学上的不对称疾病特征在神经退行性疾病的结构和功能成像中很常见,尤其是在阿尔茨海默病(AD)中。然而,对于F-18-氟脱氧葡萄糖正电子发射断层扫描(F-18-FDG-PET),不对称神经元变性及其对临床发现的影响的标准化临床评估仅偶尔被研究。本研究旨在通过详细的临床测试评估侧化神经元变性对AD检测的影响。此外,我们比较了FDG-PET低代谢和海马萎缩之间临床评估与侧化神经元变性的关联。最后,我们研究了特定子测试是否与侧化神经元变性相关。
146例临床诊断为AD的患者(年龄71±8岁)接受了FDG-PET和“阿尔茨海默病注册协会”(CERAD)测试组的检查。为了评估神经元变性,通过视觉(3D表面投影)和半定量分析对AD中通常受影响的脑区的FDG-PET低代谢进行分级。磁共振断层扫描(MRI)中海马的不对称性(左右)通过Scheltens量表进行视觉评分。计算不对称性测量值以量化侧化神经元变性,随后将不对称性评分与CERAD相关联。
FDG-PET中以左侧为主的神经元变性的不对称性在控制年龄、性别、教育年限和神经元变性总负担时是认知障碍的独立预测因子(视觉:r = -0.288,P < 0.001;半定量:r = -0.451,P < 0.001),而MRI中海马不对称性则不是(r = -0.034;P = 0.731)。对右侧和左侧侧化神经元变性病例中CERAD-PET关联的直接比较估计右侧侧化病例的检测差距为2.7年。左侧半球神经元变性与CERAD总分和多个子分数显著相关,而只有简易精神状态检查表(MMSE)(半定量:r = 0.429,P < 0.001)和构图实践(半定量:r = 0.292,P = 0.008)与右侧半球神经元变性显著相关。
脑葡萄糖代谢恶化的不对称性对神经元变性与认知功能之间的耦合有显著影响。右侧占主导的神经元变性在整体CERAD测试中显示出检测延迟,需要对认知测试的特定子领域进行评估。