Cargando…
Clinical impact of amyloid PET using (18)F-florbetapir in patients with cognitive impairment and suspected Alzheimer’s disease: a multicenter study
OBJECTIVE: Amyloid positron emission tomography (PET) can reliably detect senile plaques and fluorinated ligands are approved for clinical use. However, the clinical impact of amyloid PET imaging is still under investigation. The aim of this study was to evaluate the diagnostic impact and clinical u...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668773/ https://www.ncbi.nlm.nih.gov/pubmed/36194355 http://dx.doi.org/10.1007/s12149-022-01792-y |
_version_ | 1784831985813815296 |
---|---|
author | Matsuda, Hiroshi Okita, Kyoji Motoi, Yumiko Mizuno, Toshiki Ikeda, Manabu Sanjo, Nobuo Murakami, Koji Kambe, Taiki Takayama, Toshiki Yamada, Kei Suehiro, Takashi Matsunaga, Keiko Yokota, Takanori Tateishi, Ukihide Shigemoto, Yoko Kimura, Yukio Chiba, Emiko Kawashima, Takahiro Tomo, Yui Tachimori, Hisateru Kimura, Yuichi Sato, Noriko |
author_facet | Matsuda, Hiroshi Okita, Kyoji Motoi, Yumiko Mizuno, Toshiki Ikeda, Manabu Sanjo, Nobuo Murakami, Koji Kambe, Taiki Takayama, Toshiki Yamada, Kei Suehiro, Takashi Matsunaga, Keiko Yokota, Takanori Tateishi, Ukihide Shigemoto, Yoko Kimura, Yukio Chiba, Emiko Kawashima, Takahiro Tomo, Yui Tachimori, Hisateru Kimura, Yuichi Sato, Noriko |
author_sort | Matsuda, Hiroshi |
collection | PubMed |
description | OBJECTIVE: Amyloid positron emission tomography (PET) can reliably detect senile plaques and fluorinated ligands are approved for clinical use. However, the clinical impact of amyloid PET imaging is still under investigation. The aim of this study was to evaluate the diagnostic impact and clinical utility in patient management of amyloid PET using (18)F-florbetapir in patients with cognitive impairment and suspected Alzheimer’s disease (AD). We also aimed to determine the cutoffs for amyloid positivity for quantitative measures by investigating the agreement between quantitative and visual assessments. METHODS: Ninety-nine patients suspected of having AD underwent (18)F-florbetapir PET at five institutions. Site-specialized physicians provided a diagnosis of AD or non-AD with a percentage estimate of their confidence and their plan for patient management in terms of medication, prescription dosage, additional diagnostic tests, and care planning both before and after receiving the amyloid imaging results. A PET image for each patient was visually assessed and dichotomously rated as either amyloid-positive or amyloid-negative by four board-certified nuclear medicine physicians. The PET images were also quantitatively analyzed using the standardized uptake value ratio (SUVR) and Centiloid (CL) scale. RESULTS: Visual interpretation obtained 48 positive and 51 negative PET scans. The amyloid PET results changed the AD and non-AD diagnosis in 39 of 99 patients (39.3%). The change rates of 26 of the 54 patients (48.1%) with a pre-scan AD diagnosis were significantly higher than those of 13 of the 45 patients with a pre-scan non-AD diagnosis (χ(2) = 5.334, p = 0.0209). Amyloid PET results also resulted in at least one change to the patient management plan in 42 patients (42%), mainly medication (20 patients, 20%) and care planning (25 patients, 25%). Receiver-operating characteristic analysis determined the best agreement of the quantitative assessments and visual interpretation of PET scans to have an area under the curve of 0.993 at an SUVR of 1.19 and CL of 25.9. CONCLUSION: Amyloid PET using (18)F-florbetapir PET had a substantial clinical impact on AD and non-AD diagnosis and on patient management by enhancing diagnostic confidence. In addition, the quantitative measures may improve the visual interpretation of amyloid positivity. |
format | Online Article Text |
id | pubmed-9668773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-96687732022-11-18 Clinical impact of amyloid PET using (18)F-florbetapir in patients with cognitive impairment and suspected Alzheimer’s disease: a multicenter study Matsuda, Hiroshi Okita, Kyoji Motoi, Yumiko Mizuno, Toshiki Ikeda, Manabu Sanjo, Nobuo Murakami, Koji Kambe, Taiki Takayama, Toshiki Yamada, Kei Suehiro, Takashi Matsunaga, Keiko Yokota, Takanori Tateishi, Ukihide Shigemoto, Yoko Kimura, Yukio Chiba, Emiko Kawashima, Takahiro Tomo, Yui Tachimori, Hisateru Kimura, Yuichi Sato, Noriko Ann Nucl Med Original Article OBJECTIVE: Amyloid positron emission tomography (PET) can reliably detect senile plaques and fluorinated ligands are approved for clinical use. However, the clinical impact of amyloid PET imaging is still under investigation. The aim of this study was to evaluate the diagnostic impact and clinical utility in patient management of amyloid PET using (18)F-florbetapir in patients with cognitive impairment and suspected Alzheimer’s disease (AD). We also aimed to determine the cutoffs for amyloid positivity for quantitative measures by investigating the agreement between quantitative and visual assessments. METHODS: Ninety-nine patients suspected of having AD underwent (18)F-florbetapir PET at five institutions. Site-specialized physicians provided a diagnosis of AD or non-AD with a percentage estimate of their confidence and their plan for patient management in terms of medication, prescription dosage, additional diagnostic tests, and care planning both before and after receiving the amyloid imaging results. A PET image for each patient was visually assessed and dichotomously rated as either amyloid-positive or amyloid-negative by four board-certified nuclear medicine physicians. The PET images were also quantitatively analyzed using the standardized uptake value ratio (SUVR) and Centiloid (CL) scale. RESULTS: Visual interpretation obtained 48 positive and 51 negative PET scans. The amyloid PET results changed the AD and non-AD diagnosis in 39 of 99 patients (39.3%). The change rates of 26 of the 54 patients (48.1%) with a pre-scan AD diagnosis were significantly higher than those of 13 of the 45 patients with a pre-scan non-AD diagnosis (χ(2) = 5.334, p = 0.0209). Amyloid PET results also resulted in at least one change to the patient management plan in 42 patients (42%), mainly medication (20 patients, 20%) and care planning (25 patients, 25%). Receiver-operating characteristic analysis determined the best agreement of the quantitative assessments and visual interpretation of PET scans to have an area under the curve of 0.993 at an SUVR of 1.19 and CL of 25.9. CONCLUSION: Amyloid PET using (18)F-florbetapir PET had a substantial clinical impact on AD and non-AD diagnosis and on patient management by enhancing diagnostic confidence. In addition, the quantitative measures may improve the visual interpretation of amyloid positivity. Springer Nature Singapore 2022-10-04 2022 /pmc/articles/PMC9668773/ /pubmed/36194355 http://dx.doi.org/10.1007/s12149-022-01792-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 | Original Article Matsuda, Hiroshi Okita, Kyoji Motoi, Yumiko Mizuno, Toshiki Ikeda, Manabu Sanjo, Nobuo Murakami, Koji Kambe, Taiki Takayama, Toshiki Yamada, Kei Suehiro, Takashi Matsunaga, Keiko Yokota, Takanori Tateishi, Ukihide Shigemoto, Yoko Kimura, Yukio Chiba, Emiko Kawashima, Takahiro Tomo, Yui Tachimori, Hisateru Kimura, Yuichi Sato, Noriko Clinical impact of amyloid PET using (18)F-florbetapir in patients with cognitive impairment and suspected Alzheimer’s disease: a multicenter study |
title | Clinical impact of amyloid PET using (18)F-florbetapir in patients with cognitive impairment and suspected Alzheimer’s disease: a multicenter study |
title_full | Clinical impact of amyloid PET using (18)F-florbetapir in patients with cognitive impairment and suspected Alzheimer’s disease: a multicenter study |
title_fullStr | Clinical impact of amyloid PET using (18)F-florbetapir in patients with cognitive impairment and suspected Alzheimer’s disease: a multicenter study |
title_full_unstemmed | Clinical impact of amyloid PET using (18)F-florbetapir in patients with cognitive impairment and suspected Alzheimer’s disease: a multicenter study |
title_short | Clinical impact of amyloid PET using (18)F-florbetapir in patients with cognitive impairment and suspected Alzheimer’s disease: a multicenter study |
title_sort | clinical impact of amyloid pet using (18)f-florbetapir in patients with cognitive impairment and suspected alzheimer’s disease: a multicenter study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668773/ https://www.ncbi.nlm.nih.gov/pubmed/36194355 http://dx.doi.org/10.1007/s12149-022-01792-y |
work_keys_str_mv | AT matsudahiroshi clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT okitakyoji clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT motoiyumiko clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT mizunotoshiki clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT ikedamanabu clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT sanjonobuo clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT murakamikoji clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT kambetaiki clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT takayamatoshiki clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT yamadakei clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT suehirotakashi clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT matsunagakeiko clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT yokotatakanori clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT tateishiukihide clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT shigemotoyoko clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT kimurayukio clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT chibaemiko clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT kawashimatakahiro clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT tomoyui clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT tachimorihisateru clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT kimurayuichi clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy AT satonoriko clinicalimpactofamyloidpetusing18fflorbetapirinpatientswithcognitiveimpairmentandsuspectedalzheimersdiseaseamulticenterstudy |