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Direct comparison of brain [(18)F]FDG images acquired by SiPM-based and PMT-based PET/CT: phantom and clinical studies

BACKGROUND: Silicon photomultiplier-positron emission tomography (SiPM-PET) has better sensitivity, spatial resolution, and timing resolution than photomultiplier tube (PMT)-PET. The present study aimed to clarify the advantages of SiPM-PET in (18)F-fluoro-2-deoxy-D-glucose ([(18)F]FDG) brain imagin...

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Detalles Bibliográficos
Autores principales: Wagatsuma, Kei, Sakata, Muneyuki, Ishibashi, Kenji, Hirayama, Akira, Kawakami, Hirofumi, Miwa, Kenta, Suzuki, Yukihisa, Ishii, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683764/
https://www.ncbi.nlm.nih.gov/pubmed/33226451
http://dx.doi.org/10.1186/s40658-020-00337-4
Descripción
Sumario:BACKGROUND: Silicon photomultiplier-positron emission tomography (SiPM-PET) has better sensitivity, spatial resolution, and timing resolution than photomultiplier tube (PMT)-PET. The present study aimed to clarify the advantages of SiPM-PET in (18)F-fluoro-2-deoxy-D-glucose ([(18)F]FDG) brain imaging in a head-to-head comparison with PMT-PET in phantom and clinical studies. METHODS: Contrast was calculated from images acquired from a Hoffman 3D brain phantom, and image noise and uniformity were calculated from images acquired from a pool phantom using SiPM- and PMT-PET. Sequential PMT-PET and SiPM-PET [(18)F]FDG images were acquired over a period of 10 min from 22 controls and 10 patients. All images were separately normalized to a standard [(18)F]FDG PET template, then the mean standardized uptake values (SUV(mean)) and Z-score were calculated using MIMneuro and CortexID Suite, respectively. RESULTS: Image contrast, image noise, and uniformity in SiPM-PET changed 19.2, 3.5, and − 40.0% from PMT-PET, respectively. These physical indices of both PET scanners satisfied the criteria for acceptable image quality published by the Japanese Society of Nuclear Medicine of contrast > 55%, CV ≤ 15%, and SD ≤ 0.0249, respectively. Contrast was 70.0% for SiPM-PET without TOF and 59.5% for PMT-PET without TOF. The TOF improved contrast by 3.5% in SiPM-PET. The SUV(mean) using SiPM-PET was significantly higher than PMT-PET and did not correlate with a time delay. Z-scores were also significantly higher in images acquired from SiPM-PET (except for the bilateral posterior cingulate) than PMT-PET because the peak signal that was extracted by the calculation of Z-score in CortexID Suite was increased. The hypometabolic area in statistical maps was reduced and localized using SiPM-PET. The trend was independent of whether the images were derived from controls or patients. CONCLUSIONS: The improved spatial resolution and sensitivity of SiPM-PET contributed to better image contrast and uniformity in brain [(18)F]FDG images. The SiPM-PET offers better quality and more accurate quantitation of brain PET images. The SUV(mean) and Z-scores were higher in SiPM-PET than PMT-PET due to improved PVE. [(18)F]FDG images acquired using SiPM-PET will help to improve diagnostic outcomes based on statistical image analysis because SiPM-PET would localize the distribution of glucose metabolism on Z-score maps. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40658-020-00337-4.