Test-retest variability of adenosine A2A binding in the human brain with 11C-TMSX and PET

被引:11
作者
Naganawa, Mika [1 ,2 ]
Mishina, Masahiro [2 ,3 ]
Sakata, Muneyuki [2 ]
Oda, Keiichi [4 ]
Hiura, Mikio [5 ]
Ishii, Kenji [2 ]
Ishiwata, Kiichi [2 ]
机构
[1] Yale Univ, Sch Med, PET Ctr, New Haven, CT 06520 USA
[2] Tokyo Metropolitan Inst Gerontol, Res Team Neuroimaging, Tokyo 1730015, Japan
[3] Nippon Med Sch, Grad Sch Med, Dept Neurol Sci, Tokyo 1130022, Japan
[4] Hokkaido Univ Sci, Fac Hlth Sci, Dept Radiol Technol, Sapporo, Hokkaido 0068585, Japan
[5] Hosei Univ, Fac Sports & Hlth Studies, Tokyo 1940298, Japan
来源
EJNMMI RESEARCH | 2014年 / 4卷
基金
日本学术振兴会;
关键词
Adenosine A(2A) receptor; Positron emission tomography; C-11-TMSX; Reproducibility; POSITRON-EMISSION-TOMOGRAPHY; IN-VIVO QUANTIFICATION; RECEPTOR ANTAGONIST; GRAPHICAL ANALYSIS; LIGAND; RAT;
D O I
10.1186/s13550-014-0076-9
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: The goal of the present study was to evaluate the reproducibility of cerebral adenosine A(2A) receptor (A(2A)R) quantification using C-11-TMSX and PET in a test-retest study. Methods: Five healthy volunteers were studied twice. The test-retest variability was assessed for distribution volume (V-T) and binding potential relative to non-displaceable uptake (BPND) based on either metabolite-corrected arterial blood sampling or a reference region. The cerebral cortex and centrum semiovale were used as candidate reference regions. Results: Test-retest variability of V-T was good in all regions (6% to 13%). In the putamen, BPND using the centrum semiovale displayed a lower test-retest variability (3%) than that of BPND using the cerebral cortex as a reference region (5%). The noninvasive method showed a higher or similar level of test-retest reproducibility compared to the invasive method. Conclusions: Binding reproducibility is sufficient to use C-11-TMSX as a tool to measure the change in A(2A)R in the human brain.
引用
收藏
页数:8
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