{"title":"Brain 11C-ITMM PET to longitudinally assess type 1 metabotropic glutamate receptor availability in Alzheimer's disease","authors":"Kenji Ishibashi, Yoshiharu Miura, Kei Wagatsuma, Masashi Kameyama, Kenji Ishii","doi":"10.1111/jon.12895","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background and Purpose</h3>\n \n <p>Little evidence exists on the role of type 1 metabotropic glutamate receptor (mGluR1) in the pathophysiology of Alzheimer's disease (AD), although mGluR1 may be involved in the regulation of neuronal excitability and synaptic plasticity. We have recently reported that mGluR1 availability in the early stage of AD is equivalent to that in healthy subjects. This study aimed to address whether mGluR1 availability changes with the progression of AD.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Eight patients with AD (79.1 ± 4.6 years) underwent a total of two positron emission tomography (PET) examinations using the mGluR1 radioligand during the early-to-middle stages of AD. The mean interval was 2.8 years. Volumes-of-interest were placed on the frontal, parietal, and temporal cortices, hippocampus, anterior and posterior lobes, and vermis in the cerebellum. The binding potential (BP<sub>ND</sub>) was calculated to estimate mGluR1 availability, applying partial volume correction to the BP<sub>ND</sub> values.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>No significant difference was observed in BP<sub>ND</sub> values between the first and second PET examinations in the frontal cortex (<i>p</i> = 0.94), parietal cortex (<i>p</i> = 0.67), temporal cortex (<i>p</i> = 0.20), hippocampus (<i>p</i> = 0.17), anterior lobe (<i>p</i> = 0.73), posterior lobe (<i>p</i> = 0.21), and vermis (<i>p</i> = 0.22).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>This study suggests that mGluR1 availability is unchanged in the follow-up period of a few years during the early-to-middle stages of AD.</p>\n </section>\n </div>","PeriodicalId":16399,"journal":{"name":"Journal of Neuroimaging","volume":"31 5","pages":"864-868"},"PeriodicalIF":2.3000,"publicationDate":"2021-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/jon.12895","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neuroimaging","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jon.12895","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 1
Abstract
Background and Purpose
Little evidence exists on the role of type 1 metabotropic glutamate receptor (mGluR1) in the pathophysiology of Alzheimer's disease (AD), although mGluR1 may be involved in the regulation of neuronal excitability and synaptic plasticity. We have recently reported that mGluR1 availability in the early stage of AD is equivalent to that in healthy subjects. This study aimed to address whether mGluR1 availability changes with the progression of AD.
Methods
Eight patients with AD (79.1 ± 4.6 years) underwent a total of two positron emission tomography (PET) examinations using the mGluR1 radioligand during the early-to-middle stages of AD. The mean interval was 2.8 years. Volumes-of-interest were placed on the frontal, parietal, and temporal cortices, hippocampus, anterior and posterior lobes, and vermis in the cerebellum. The binding potential (BPND) was calculated to estimate mGluR1 availability, applying partial volume correction to the BPND values.
Results
No significant difference was observed in BPND values between the first and second PET examinations in the frontal cortex (p = 0.94), parietal cortex (p = 0.67), temporal cortex (p = 0.20), hippocampus (p = 0.17), anterior lobe (p = 0.73), posterior lobe (p = 0.21), and vermis (p = 0.22).
Conclusion
This study suggests that mGluR1 availability is unchanged in the follow-up period of a few years during the early-to-middle stages of AD.
期刊介绍:
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