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Early-phase (18)F-FP-CIT and (18)F-flutemetamol PET were significantly correlated
Little is known about whether early-phase PET images of (18)F-FP-CIT match those of amyloid PET. Here, we compared early-phase (18)F-FP-CIT and (18)F-flutemetamol PET images in patients who underwent both within a 1-month interval. The SUVR on early-phase (18)F-FP-CIT PET (median, 0.86) was signific...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192502/ https://www.ncbi.nlm.nih.gov/pubmed/34112926 http://dx.doi.org/10.1038/s41598-021-91891-z |
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author | An, Young-Sil Yoon, Jung Han Son, Sang Joon Hong, Chang Hyung Lee, Su Jin Yoon, Joon-Kee |
author_facet | An, Young-Sil Yoon, Jung Han Son, Sang Joon Hong, Chang Hyung Lee, Su Jin Yoon, Joon-Kee |
author_sort | An, Young-Sil |
collection | PubMed |
description | Little is known about whether early-phase PET images of (18)F-FP-CIT match those of amyloid PET. Here, we compared early-phase (18)F-FP-CIT and (18)F-flutemetamol PET images in patients who underwent both within a 1-month interval. The SUVR on early-phase (18)F-FP-CIT PET (median, 0.86) was significantly lower than that of (18)F-flutemetamol PET (median, 0.91, p < 0.001) for total brain regions including all cerebral lobes and central structures. This significant difference persisted for each brain region except central structures (p = 0.232). The SUVR of total brain regions obtained from early (18)F-FP-CIT PET showed a very strong correlation with that of (18)F-flutemetamol PET (rho = 0.80, p < 0.001). Among the kinetic parameters, only R1 showed a statistically significant correlation between the two techniques for all brain regions (rho = 0.89, p < 0.001). R1 from (18)F-FP-CIT (median, 0.77) was significantly lower in all areas of the brain compared to R1 from (18)F-flutemetamol PET (median, 0.81, p < 0.001).(18)F-FP-CIT demonstrated lower uptake in cortical brain regions than (18)F-flutemetamol on early-phase PET. However, both early-phase PETs demonstrated significant correlation of uptake. |
format | Online Article Text |
id | pubmed-8192502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81925022021-06-14 Early-phase (18)F-FP-CIT and (18)F-flutemetamol PET were significantly correlated An, Young-Sil Yoon, Jung Han Son, Sang Joon Hong, Chang Hyung Lee, Su Jin Yoon, Joon-Kee Sci Rep Article Little is known about whether early-phase PET images of (18)F-FP-CIT match those of amyloid PET. Here, we compared early-phase (18)F-FP-CIT and (18)F-flutemetamol PET images in patients who underwent both within a 1-month interval. The SUVR on early-phase (18)F-FP-CIT PET (median, 0.86) was significantly lower than that of (18)F-flutemetamol PET (median, 0.91, p < 0.001) for total brain regions including all cerebral lobes and central structures. This significant difference persisted for each brain region except central structures (p = 0.232). The SUVR of total brain regions obtained from early (18)F-FP-CIT PET showed a very strong correlation with that of (18)F-flutemetamol PET (rho = 0.80, p < 0.001). Among the kinetic parameters, only R1 showed a statistically significant correlation between the two techniques for all brain regions (rho = 0.89, p < 0.001). R1 from (18)F-FP-CIT (median, 0.77) was significantly lower in all areas of the brain compared to R1 from (18)F-flutemetamol PET (median, 0.81, p < 0.001).(18)F-FP-CIT demonstrated lower uptake in cortical brain regions than (18)F-flutemetamol on early-phase PET. However, both early-phase PETs demonstrated significant correlation of uptake. Nature Publishing Group UK 2021-06-10 /pmc/articles/PMC8192502/ /pubmed/34112926 http://dx.doi.org/10.1038/s41598-021-91891-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article An, Young-Sil Yoon, Jung Han Son, Sang Joon Hong, Chang Hyung Lee, Su Jin Yoon, Joon-Kee Early-phase (18)F-FP-CIT and (18)F-flutemetamol PET were significantly correlated |
title | Early-phase (18)F-FP-CIT and (18)F-flutemetamol PET were significantly correlated |
title_full | Early-phase (18)F-FP-CIT and (18)F-flutemetamol PET were significantly correlated |
title_fullStr | Early-phase (18)F-FP-CIT and (18)F-flutemetamol PET were significantly correlated |
title_full_unstemmed | Early-phase (18)F-FP-CIT and (18)F-flutemetamol PET were significantly correlated |
title_short | Early-phase (18)F-FP-CIT and (18)F-flutemetamol PET were significantly correlated |
title_sort | early-phase (18)f-fp-cit and (18)f-flutemetamol pet were significantly correlated |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192502/ https://www.ncbi.nlm.nih.gov/pubmed/34112926 http://dx.doi.org/10.1038/s41598-021-91891-z |
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