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Determination of Starting Time in Logan Graphical Analysis Using the Runs Test for Quantitative PET Imaging
https://repo.qst.go.jp/records/54064
https://repo.qst.go.jp/records/54064e1a622b5-98e8-493b-91bf-f5195d5ac199
Item type | 会議発表論文 / Conference Paper(1) | |||||
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公開日 | 2008-10-24 | |||||
タイトル | ||||||
タイトル | Determination of Starting Time in Logan Graphical Analysis Using the Runs Test for Quantitative PET Imaging | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_5794 | |||||
資源タイプ | conference paper | |||||
アクセス権 | ||||||
アクセス権 | metadata only access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
著者 |
Kimura, Yuichi
× Kimura, Yuichi× Ogaki, Hiroto× Naganawa, Mika× Shidahara, Miho× Sakata, Muneyuki× Ishiwata, Kiichi× Suga, Mikio× 木村 裕一× 大柿 宏人× 長縄 美香× 志田原 美保× 坂田 宗之× 石渡 喜一× 菅 幹生 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The Logan graphical analysis (LGA) is a widely used algorithm for PET quantitative imaging. In LGA, a total distribution volume (VT) is derived as a slope in the linear relation between both radiopharmaceutical concentrations in tissues and arterial plasma after the time, t*, when the radiopharmaceutical distributes uniformly in regional tissues, and therefore t* should be specified automatically for every voxels. This study proposes a new algorithm for t* determination, ratLGA, based on the runs test, which is a nonparametric hypothesis test for randomness. In ratLGA, LGA was applied to compute residuals for the line estimation with a set of feasible t* for PET studies. Then, the runs test was employed to decide the randomness of signs in the residuals with a significance level of 0.05. ratLGA is expected to be robust against the noise observed in voxel-based tTACs. Using t* (5 to 80 [min]), ratLGA was applied to the simulated and clinical data for 11C-SA4503, which is a ligand for the sigma1 receptors (Sakata, NeuroImage, 2007). In the simulation, VT was widely ranged from 10 to 60 [mL/cm3] considering the kinetics of SA4503, and the linear regressions for estimated VT were y=0.94x-1.23 in ratLGA and y=0.81x+3.80 when t* was fixed at 30 [min] (Sakata, 2007). The underestimation was improved by ratLGA. ratLGA increased a contrast in clinical VT images as shown in figures. Figures A and B were VT in case of ratLGA and the fixed t*, respectively, and Figure C showed the difference. In conclusion, the runs test is promising to determine t* for LGA. |
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書誌情報 |
World Molecular Imaging Congress 巻 2008, p. 0506, 発行日 2008-09 |