11C-PBR28 binding to translocator protein increases with progression of Alzheimer's disease

被引:133
作者
Kreisl, William C. [1 ,4 ]
Lyoo, Chul Hyoung [1 ,5 ]
Liow, Jeih-San [1 ]
Wei, Monica [1 ]
Snow, Joseph [2 ]
Page, Emily [1 ]
Jenko, Kimberly J. [1 ]
Morse, Cheryl L. [1 ]
Zoghbi, Sami S. [1 ]
Pike, Victor W. [1 ]
Turner, R. Scott [3 ]
Innis, Robert B. [1 ]
机构
[1] NIMH, Mol Imaging Branch, Bethesda, MD 20892 USA
[2] NIMH, Off Clin Director, Bethesda, MD 20892 USA
[3] Georgetown Univ, Memory Disorders Program, Washington, DC USA
[4] Columbia Univ, Taub Inst, Med Ctr, 622 W 168th St,PH 19th Floor, New York, NY 10032 USA
[5] Yonsei Univ, Dept Neurol, Gangnam Severance Hosp, Coll Med, Seoul 120749, South Korea
基金
美国国家卫生研究院;
关键词
Alzheimer's disease; Neuroinflammation; PET imaging; MILD COGNITIVE IMPAIRMENT; VIVO RADIOLIGAND BINDING; MICROGLIAL ACTIVATION; HUMAN BRAIN; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; COMPOUND B; 18; KDA; RECOMMENDATIONS;
D O I
10.1016/j.neurobiolaging.2016.04.011
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
This longitudinal study sought to determine whether the 18 kDa translocator protein (TSPO), a marker of neuroinflammation, increases over time in Alzheimer's disease. Positron emission tomography imaging with the TSPO radioligand C-11-PBR28 was performed at baseline and after a median follow-up of 2.7 years in 14 amyloid-positive patients and 8 amyloid-negative controls. Patients had a greater increase in TSPO binding than controls in inferior parietal lobule, precuneus, occipital cortex, hippocampus, entorhinal cortex, and combined middle and inferior temporal cortex. TSPO binding in temporoparietal regions increased from 3.9% to 6.3% per annum in patients, but ranged from -0.5% to 1% per annum in controls. The change in TSPO binding correlated with cognitive worsening on clinical dementia rating scale-sum of boxes and reduced cortical volume. The annual rate of increased TSPO binding in temporoparietal regions was about 5-fold higher in patients with clinical progression (n = 9) compared with those who did not progress (n = 5). TSPO may serve as a biomarker of Alzheimer's progression and response to anti-inflammatory therapies. Published by Elsevier Inc.
引用
收藏
页码:53 / 61
页数:9
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