Parametric Methods for Dynamic 11 C-Phenytoin PET Studies

In this study, the performance of various methods for generating quantitative parametric images of dynamic C-phenytoin PET studies was evaluated. Double-baseline 60-min dynamic C-phenytoin PET studies, including online arterial sampling, were acquired for 6 healthy subjects. Parametric images were g...

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Bibliographic Details
Published inJournal of Nuclear Medicine Vol. 58; no. 3; pp. 479 - 483
Main Authors Mansor, Syahir, Yaqub, Maqsood, Boellaard, Ronald, Froklage, Femke E., de Vries, Anke, Bakker, Esther D.M., Voskuyl, Rob A., Eriksson, Jonas, Schwarte, Lothar A., Verbeek, Joost, Windhorst, Albert D., Lammertsma, Adriaan A.
Format Journal Article
LanguageEnglish
Published United States 01.03.2017
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Summary:In this study, the performance of various methods for generating quantitative parametric images of dynamic C-phenytoin PET studies was evaluated. Double-baseline 60-min dynamic C-phenytoin PET studies, including online arterial sampling, were acquired for 6 healthy subjects. Parametric images were generated using Logan plot analysis, a basis function method, and spectral analysis. Parametric distribution volume (V ) and influx rate ( ) were compared with those obtained from nonlinear regression analysis of time-activity curves. In addition, global and regional test-retest (TRT) variability was determined for parametric and V values. Biases in V observed with all parametric methods were less than 5%. For , spectral analysis showed a negative bias of 16%. The mean TRT variabilities of V and were less than 10% for all methods. Shortening the scan duration to 45 min provided similar V and with comparable TRT performance compared with 60-min data. Among the various parametric methods tested, the basis function method provided parametric V and values with the least bias compared with nonlinear regression data and showed TRT variabilities lower than 5%, also for smaller volume-of-interest sizes (i.e., higher noise levels) and shorter scan duration.
ISSN:0161-5505
2159-662X
1535-5667
DOI:10.2967/jnumed.116.178707