全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
-  2019 

Unchanged type 1 metabotropic glutamate receptor availability in patients with Alzheimer's disease: A study using 11C-ITMM positron emission tomography

DOI: 10.1016/j.nicl.2019.101783

Keywords: Type 1 metabotropic glutamate receptor, Alzheimer's disease, PET, 11C-ITMM

Full-Text   Cite this paper   Add to My Lib

Abstract:

Imaging of type 1 metabotropic glutamate receptor (mGluR1) has recently become possible using positron emission tomography (PET). To date, little evidence exists on the role of mGluR1 in the pathophysiology of Alzheimer's disease (AD). We aimed to examine mGluR1 availability in patients with AD. Ten patients with AD (78.9?±?5.9?years) and 12 age-matched volunteers (74.6?±?2.6?years) underwent PET using an mGluR1 radiotracer. All patients were anti-dementia drug-naive. Volumes-of-interest were placed on the anterior and posterior lobes and vermis in the cerebellum and frontal, parietal, and temporal cortices. The binding potential (BPND) was calculated to estimate mGluR1 availability, and partial volume correction was applied to the BPND values. Mini Mental State Examination (MMSE) scores were also obtained (22.0?±?4.8). No significant difference was observed in BPND between the AD and control groups in the anterior lobe (p?=?.30), posterior lobe (p?=?.95), vermis (p?=?.96), frontal cortex (p?=?.61), parietal cortex (p?=?.59), or temporal cortex (p?=?.27). No significant correlation was observed between BPND and MMSE scores in the anterior lobe (p?=?.59), posterior lobe (p?=?.35), vermis (p?=?.92), frontal cortex (p?=?.78), parietal cortex (p?=?.83), or temporal cortex (p?=?.82). In conclusions, this study suggests that mGluR1 availability is unchanged in the relatively early stage of AD. However, because regional mGluR1 availability may change with the progression of AD, further longitudinal follow-up is necessary

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133

WeChat 1538708413