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(18)F-FPYBF-2, a new F-18-labelled amyloid imaging PET tracer: first experience in 61 volunteers and 55 patients with dementia
OBJECTIVE: Recently, we developed a benzofuran derivative for the imaging of β-amyloid plaques, 5-(5-(2-(2-(2-(18)F-fluoroethoxy)ethoxy)ethoxy)benzofuran-2-yl)-N-methylpyridin-2-amine ((18)F-FPYBF-2) (Ono et al., J Med Chem 54:2971–9, 2011). The aim of this study was to assess the feasibility of (18...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Japan
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852179/ https://www.ncbi.nlm.nih.gov/pubmed/29388083 http://dx.doi.org/10.1007/s12149-018-1236-1 |
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author | Higashi, Tatsuya Nishii, Ryuichi Kagawa, Shinya Kishibe, Yoshihiko Takahashi, Masaaki Okina, Tomoko Suzuki, Norio Hasegawa, Hiroshi Nagahama, Yasuhiro Ishizu, Koichi Oishi, Naoya Kimura, Hiroyuki Watanabe, Hiroyuki Ono, Masahiro Saji, Hideo Yamauchi, Hiroshi |
author_facet | Higashi, Tatsuya Nishii, Ryuichi Kagawa, Shinya Kishibe, Yoshihiko Takahashi, Masaaki Okina, Tomoko Suzuki, Norio Hasegawa, Hiroshi Nagahama, Yasuhiro Ishizu, Koichi Oishi, Naoya Kimura, Hiroyuki Watanabe, Hiroyuki Ono, Masahiro Saji, Hideo Yamauchi, Hiroshi |
author_sort | Higashi, Tatsuya |
collection | PubMed |
description | OBJECTIVE: Recently, we developed a benzofuran derivative for the imaging of β-amyloid plaques, 5-(5-(2-(2-(2-(18)F-fluoroethoxy)ethoxy)ethoxy)benzofuran-2-yl)-N-methylpyridin-2-amine ((18)F-FPYBF-2) (Ono et al., J Med Chem 54:2971–9, 2011). The aim of this study was to assess the feasibility of (18)F-FPYBF-2 as an amyloid imaging PET tracer in a first clinical study with healthy volunteers and patients with various dementia and in comparative dual tracer study using (11)C-Pittsburgh Compound B ((11)C-PiB). METHODS: 61 healthy volunteers (age: 53.7 ± 13.1 years old; 19 male and 42 female; age range 24–79) and 55 patients with suspected dementia [Alzheimer’s Disease (AD); early AD: n = 19 and moderate stage AD: n = 8, other dementia: n = 9, mild cognitive impairment (MCI): n = 16, cognitively normal: n = 3] for first clinical study underwent static head PET/CT scan using (18)F(−)FPYBF-2 at 50–70 min after injection. 13 volunteers and 14 patients also underwent dynamic PET scan at 0–50 min at the same instant. 16 subjects (volunteers: n = 5, patients with dementia: n = 11) (age: 66.3 ± 14.2 years old; 10 males and 6 females) were evaluated for comparative study (50–70 min after injection) using (18)F-FPYBF-2 and (11)C-PiB on separate days, respectively. Quantitative analysis of mean cortical uptake was calculated using Mean Cortical Index of SUVR (standardized uptake value ratio) based on the established method for (11)C-PiB analysis using cerebellar cortex as control. RESULTS: Studies with healthy volunteers showed that (18)F-FPYBF-2 uptake was mainly observed in cerebral white matter and that average Mean Cortical Index at 50–70 min was low and stable (1.066 ± 0.069) basically independent from age or gender. In patients with AD, (18)F-FPYBF-2 uptake was observed both in cerebral white and gray matter, and Mean Cortical Index was significantly higher (early AD: 1.288 ± 0.134, moderate AD: 1.342 ± 0.191) than those of volunteers and other dementia (1.018 ± 0.057). In comparative study, the results of (18)F-FPYBF-2 PET/CT were comparable with those of (11)C-PiB, and the Mean Cortical Index ((18)F-FPYBF-2: 1.173 ± 0.215; (11)C-PiB: 1.435 ± 0.474) showed direct proportional relationship with each other (p < 0.0001). CONCLUSIONS: Our first clinical study suggest that (18)F-FPYBF-2 is a useful PET tracer for the evaluation of β-amyloid deposition and that quantitative analysis of Mean Cortical Index of SUVR is a reliable diagnostic tool for the diagnosis of AD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12149-018-1236-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5852179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-58521792018-03-21 (18)F-FPYBF-2, a new F-18-labelled amyloid imaging PET tracer: first experience in 61 volunteers and 55 patients with dementia Higashi, Tatsuya Nishii, Ryuichi Kagawa, Shinya Kishibe, Yoshihiko Takahashi, Masaaki Okina, Tomoko Suzuki, Norio Hasegawa, Hiroshi Nagahama, Yasuhiro Ishizu, Koichi Oishi, Naoya Kimura, Hiroyuki Watanabe, Hiroyuki Ono, Masahiro Saji, Hideo Yamauchi, Hiroshi Ann Nucl Med Original Article OBJECTIVE: Recently, we developed a benzofuran derivative for the imaging of β-amyloid plaques, 5-(5-(2-(2-(2-(18)F-fluoroethoxy)ethoxy)ethoxy)benzofuran-2-yl)-N-methylpyridin-2-amine ((18)F-FPYBF-2) (Ono et al., J Med Chem 54:2971–9, 2011). The aim of this study was to assess the feasibility of (18)F-FPYBF-2 as an amyloid imaging PET tracer in a first clinical study with healthy volunteers and patients with various dementia and in comparative dual tracer study using (11)C-Pittsburgh Compound B ((11)C-PiB). METHODS: 61 healthy volunteers (age: 53.7 ± 13.1 years old; 19 male and 42 female; age range 24–79) and 55 patients with suspected dementia [Alzheimer’s Disease (AD); early AD: n = 19 and moderate stage AD: n = 8, other dementia: n = 9, mild cognitive impairment (MCI): n = 16, cognitively normal: n = 3] for first clinical study underwent static head PET/CT scan using (18)F(−)FPYBF-2 at 50–70 min after injection. 13 volunteers and 14 patients also underwent dynamic PET scan at 0–50 min at the same instant. 16 subjects (volunteers: n = 5, patients with dementia: n = 11) (age: 66.3 ± 14.2 years old; 10 males and 6 females) were evaluated for comparative study (50–70 min after injection) using (18)F-FPYBF-2 and (11)C-PiB on separate days, respectively. Quantitative analysis of mean cortical uptake was calculated using Mean Cortical Index of SUVR (standardized uptake value ratio) based on the established method for (11)C-PiB analysis using cerebellar cortex as control. RESULTS: Studies with healthy volunteers showed that (18)F-FPYBF-2 uptake was mainly observed in cerebral white matter and that average Mean Cortical Index at 50–70 min was low and stable (1.066 ± 0.069) basically independent from age or gender. In patients with AD, (18)F-FPYBF-2 uptake was observed both in cerebral white and gray matter, and Mean Cortical Index was significantly higher (early AD: 1.288 ± 0.134, moderate AD: 1.342 ± 0.191) than those of volunteers and other dementia (1.018 ± 0.057). In comparative study, the results of (18)F-FPYBF-2 PET/CT were comparable with those of (11)C-PiB, and the Mean Cortical Index ((18)F-FPYBF-2: 1.173 ± 0.215; (11)C-PiB: 1.435 ± 0.474) showed direct proportional relationship with each other (p < 0.0001). CONCLUSIONS: Our first clinical study suggest that (18)F-FPYBF-2 is a useful PET tracer for the evaluation of β-amyloid deposition and that quantitative analysis of Mean Cortical Index of SUVR is a reliable diagnostic tool for the diagnosis of AD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12149-018-1236-1) contains supplementary material, which is available to authorized users. Springer Japan 2018-01-31 2018 /pmc/articles/PMC5852179/ /pubmed/29388083 http://dx.doi.org/10.1007/s12149-018-1236-1 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Higashi, Tatsuya Nishii, Ryuichi Kagawa, Shinya Kishibe, Yoshihiko Takahashi, Masaaki Okina, Tomoko Suzuki, Norio Hasegawa, Hiroshi Nagahama, Yasuhiro Ishizu, Koichi Oishi, Naoya Kimura, Hiroyuki Watanabe, Hiroyuki Ono, Masahiro Saji, Hideo Yamauchi, Hiroshi (18)F-FPYBF-2, a new F-18-labelled amyloid imaging PET tracer: first experience in 61 volunteers and 55 patients with dementia |
title | (18)F-FPYBF-2, a new F-18-labelled amyloid imaging PET tracer: first experience in 61 volunteers and 55 patients with dementia |
title_full | (18)F-FPYBF-2, a new F-18-labelled amyloid imaging PET tracer: first experience in 61 volunteers and 55 patients with dementia |
title_fullStr | (18)F-FPYBF-2, a new F-18-labelled amyloid imaging PET tracer: first experience in 61 volunteers and 55 patients with dementia |
title_full_unstemmed | (18)F-FPYBF-2, a new F-18-labelled amyloid imaging PET tracer: first experience in 61 volunteers and 55 patients with dementia |
title_short | (18)F-FPYBF-2, a new F-18-labelled amyloid imaging PET tracer: first experience in 61 volunteers and 55 patients with dementia |
title_sort | (18)f-fpybf-2, a new f-18-labelled amyloid imaging pet tracer: first experience in 61 volunteers and 55 patients with dementia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852179/ https://www.ncbi.nlm.nih.gov/pubmed/29388083 http://dx.doi.org/10.1007/s12149-018-1236-1 |
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