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Image-Derived Input Function for Human Brain Using High Resolution PET Imaging with [(11)C](R)-rolipram and [(11)C]PBR28

BACKGROUND: The aim of this study was to test seven previously published image-input methods in state-of-the-art high resolution PET brain images. Images were obtained with a High Resolution Research Tomograph plus a resolution-recovery reconstruction algorithm using two different radioligands with...

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Detalles Bibliográficos
Autores principales: Zanotti-Fregonara, Paolo, Liow, Jeih-San, Fujita, Masahiro, Dusch, Elodie, Zoghbi, Sami S., Luong, Elise, Boellaard, Ronald, Pike, Victor W., Comtat, Claude, Innis, Robert B.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3045425/
https://www.ncbi.nlm.nih.gov/pubmed/21364880
http://dx.doi.org/10.1371/journal.pone.0017056
Descripción
Sumario:BACKGROUND: The aim of this study was to test seven previously published image-input methods in state-of-the-art high resolution PET brain images. Images were obtained with a High Resolution Research Tomograph plus a resolution-recovery reconstruction algorithm using two different radioligands with different radiometabolite fractions. Three of the methods required arterial blood samples to scale the image-input, and four were blood-free methods. METHODS: All seven methods were tested on twelve scans with [(11)C](R)-rolipram, which has a low radiometabolite fraction, and on nineteen scans with [(11)C]PBR28 (high radiometabolite fraction). Logan V (T) values for both blood and image inputs were calculated using the metabolite-corrected input functions. The agreement of image-derived Logan V (T) values with the reference blood-derived Logan V (T) values was quantified using a scoring system. Using the image input methods that gave the most accurate results with Logan analysis, we also performed kinetic modelling with a two-tissue compartment model. RESULTS: For both radioligands the highest scores were obtained with two blood-based methods, while the blood-free methods generally performed poorly. All methods gave higher scores with [(11)C](R)-rolipram, which has a lower metabolite fraction. Compartment modeling gave less reliable results, especially for the estimation of individual rate constants. CONCLUSION: Our study shows that: 1) Image input methods that are validated for a specific tracer and a specific machine may not perform equally well in a different setting; 2) despite the use of high resolution PET images, blood samples are still necessary to obtain a reliable image input function; 3) the accuracy of image input may also vary between radioligands depending on the magnitude of the radiometabolite fraction: the higher the metabolite fraction of a given tracer (e.g., [(11)C]PBR28), the more difficult it is to obtain a reliable image-derived input function; and 4) in association with image inputs, graphical analyses should be preferred over compartmental modelling.