Literature DB >> 31584490

In Vivo Assessment of Tau Deposition in Alzheimer Disease and Assessing Its Relationship to Regional Brain Glucose Metabolism and Cognition.

Vivek Baghel1, Madhavi Tripathi1, Girish Parida1, Ravikant Gupta1, Saroj Yadav2, Praveen Kumar1, A B Dey2, Nishikant Avinash Damle1, Rajeev Kumar2, Chandrasekhar Bal1.   

Abstract

AIM: In this study, we investigated the relationship of cerebral tau deposition (F-tau-AD-ML 104 PET/CT) with glucose metabolism (F-FDG PET/CT) and cognitive function in patients with Alzheimer disease (AD). PATIENTS AND METHODS: Seventy subjects (Mini Mental State Examination [MMSE] score <18 = 37 [AD]; MMSE score, 18-24 = 16 [early AD]) and 17 controls were included in this study. All participants underwent detailed neurological and neuropsychological evaluation, followed by F-tau-AD-ML 104 and F-FDG PET/CT imaging. Region-wise SUVmax ratios at 50 to 60 minutes postinjection were calculated for F-tau-AD-ML 104 and F-FDG, using the cerebellar cortex as the reference region. Linear models were used to investigate the association of regional F-tau-AD-ML 104 retention with F-FDG uptake and cognition (MMSE scores).
RESULTS: F-Tau-AD-ML 104 retention was observed in the parietal lobe, temporal lobe, hippocampus, parahippocampus, frontal lobe, anterior and posterior cingulate, and precuneus in advanced and early AD patient as compared with normal controls with regional hypometabolism in overlapping regions on F-FDG PET. Significant negative association was found between F-tau-AD-ML 104 regional retention and glucose metabolism in the parietal lobe, temporal lobe, hippocampus, parahippocampus, frontal lobe, anterior and posterior cingulate, and precuneus among patients with advanced and early AD. In advanced and early AD patients, a negative association was found between F-tau-AD-ML 104 regional retention (precuneus) and cognition (MMSE score), whereas a positive association was observed between F-FDG regional uptake (precuneus) and cognition (MMSE score).
CONCLUSIONS: Tau pathology overlapped with areas of hypometabolism on FDG PET in the brains of AD patients. Tau deposition was found to have negative association with cognitive scores in these patients.

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Year:  2019        PMID: 31584490     DOI: 10.1097/RLU.0000000000002791

Source DB:  PubMed          Journal:  Clin Nucl Med        ISSN: 0363-9762            Impact factor:   7.794


  11 in total

1.  Neuropsychological Performance Is Correlated With Tau Protein Deposition and Glucose Metabolism in Patients With Alzheimer's Disease.

Authors:  Zhen Qiao; Guihong Wang; Xiaobin Zhao; Kai Wang; Di Fan; Qian Chen; Lin Ai
Journal:  Front Aging Neurosci       Date:  2022-05-18       Impact factor: 5.702

2.  Disruption of metabolic, sleep, and sensorimotor functional outcomes in a female transgenic mouse model of Alzheimer's disease.

Authors:  Divine C Nwafor; Sreeparna Chakraborty; Sujung Jun; Allison L Brichacek; Margaret Dransfeld; Darren E Gemoets; Duaa Dakhlallah; Candice M Brown
Journal:  Behav Brain Res       Date:  2020-11-01       Impact factor: 3.332

3.  Electroacupuncture Protects Cognition by Regulating Tau Phosphorylation and Glucose Metabolism via the AKT/GSK3β Signaling Pathway in Alzheimer's Disease Model Mice.

Authors:  Anping Xu; Qingtao Zeng; Yinshan Tang; Xin Wang; Xiaochen Yuan; You Zhou; Zhigang Li
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6.  18F-APN-1607 Tau Positron Emission Tomography Imaging for Evaluating Disease Progression in Alzheimer's Disease.

Authors:  Xiaojun Xu; Weiwei Ruan; Fang Liu; Yongkang Gai; Qingyao Liu; Ying Su; Zhihou Liang; Xun Sun; Xiaoli Lan
Journal:  Front Aging Neurosci       Date:  2022-02-10       Impact factor: 5.750

7.  Abnormal characterization of dynamic functional connectivity in Alzheimer's disease.

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Journal:  Neural Regen Res       Date:  2022-09       Impact factor: 5.135

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Authors:  Lu Yao; Shinsuke Aoyama; Atushi Ouchi; Yasuji Yamamoto; Ichiro Sora
Journal:  Neuropsychopharmacol Rep       Date:  2022-03-05

Review 9.  Clinical Utility of the Pathogenesis-Related Proteins in Alzheimer's Disease.

Authors:  Bin Zhou; Masanori Fukushima
Journal:  Int J Mol Sci       Date:  2020-11-17       Impact factor: 5.923

10.  ADMSC Exo-MicroRNA-22 improve neurological function and neuroinflammation in mice with Alzheimer's disease.

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Journal:  J Cell Mol Med       Date:  2021-07-11       Impact factor: 5.310

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