β-Amyloid binding in elderly subjects with declining or stable episodic memory function measured with PET and [11C]AZD2184

Purpose Cognitive decline has been suggested as an early marker for later onset of Alzheimer’s disease. We therefore explored the relationship between decline in episodic memory and β-amyloid using positron emission tomography (PET) and [ 11 C]AZD2184, a radioligand with potential to detect low leve...

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Published inEuropean journal of nuclear medicine and molecular imaging Vol. 42; no. 10; pp. 1507 - 1511
Main Authors Mattsson, Patrik, Forsberg, Anton, Persson, Jonas, Nyberg, Lars, Nilsson, Lars-Göran, Halldin, Christer, Farde, Lars
Format Journal Article
LanguageEnglish
Published Berlin/Heidelberg Springer Berlin Heidelberg 01.09.2015
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ISSN1619-7070
1619-7089
1619-7089
DOI10.1007/s00259-015-3103-9

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Abstract Purpose Cognitive decline has been suggested as an early marker for later onset of Alzheimer’s disease. We therefore explored the relationship between decline in episodic memory and β-amyloid using positron emission tomography (PET) and [ 11 C]AZD2184, a radioligand with potential to detect low levels of amyloid deposits. Methods Healthy elderly subjects with declining (n = 10) or stable (n = 10) episodic memory over 15 years were recruited from the population-based Betula study and examined with PET. Brain radioactivity was measured after intravenous administration of [ 11 C]AZD2184. The binding potential BP ND was calculated using linear graphical analysis with the cerebellum as reference region. Results The binding of [ 11 C]AZD2184 in total grey matter was generally low in the declining group, whereas some binding could be observed in the stable group. Mean BP ND was significantly higher in the stable group compared to the declining group (p = 0.019). An observation was that the three subjects with the highest BP ND were ApoE ε4 allele carriers. Conclusions We conclude that cognitive decline in the general population does not seem to stand by itself as an early predictor for amyloid deposits.
AbstractList Purpose: Cognitive decline has been suggested as an early marker for later onset of Alzheimer's disease. We therefore explored the relationship between decline in episodic memory and β-amyloid using positron emission tomography (PET) and [ 11 C]AZD2184, a radioligand with potential to detect low levels of amyloid deposits. Methods: Healthy elderly subjects with declining (n = 10) or stable (n = 10) episodic memory over 15 years were recruited from the population-based Betula study and examined with PET. Brain radioactivity was measured after intravenous administration of [ 11 C]AZD2184 The binding potential  BP ND was calculated using linear graphical analysis with the cerebellum as reference region. Results: The binding of [ 11 C]AZD2184 in total grey matter was generally low in the declining group, whereas some binding could be observed in the stable group. Mean  BP ND was significantly higher in the stable group compared to the declining group (p = 0.019). An observation was that the three subjects with the highest BPND were ApoE ε4 allele carriers. Conclusions: We conclude that cognitive decline in the general population does not seem to stand by itself as an early predictor for amyloid deposits.
Purpose Cognitive decline has been suggested as an early marker for later onset of Alzheimer's disease. We therefore explored the relationship between decline in episodic memory and beta-amyloid using positron emission tomography (PET) and [C-11]AZD2184, a radioligand with potential to detect low levels of amyloid deposits. Methods Healthy elderly subjects with declining (n = 10) or stable (n = 10) episodic memory over 15 years were recruited from the population-based Betula study and examined with PET. Brain radioactivity was measured after intravenous administration of [C-11]AZD2184. The binding potential BP (ND) was calculated using linear graphical analysis with the cerebellum as reference region. Results The binding of [C-11]AZD2184 in total grey matter was generally low in the declining group, whereas some binding could be observed in the stable group. Mean BP (ND) was significantly higher in the stable group compared to the declining group (p = 0.019). An observation was that the three subjects with the highest BPND were ApoE epsilon 4 allele carriers. Conclusions We conclude that cognitive decline in the general population does not seem to stand by itself as an early predictor for amyloid deposits.
Cognitive decline has been suggested as an early marker for later onset of Alzheimer's disease. We therefore explored the relationship between decline in episodic memory and β-amyloid using positron emission tomography (PET) and [(11)C]AZD2184, a radioligand with potential to detect low levels of amyloid deposits. Healthy elderly subjects with declining (n = 10) or stable (n = 10) episodic memory over 15 years were recruited from the population-based Betula study and examined with PET. Brain radioactivity was measured after intravenous administration of [(11)C]AZD2184. The binding potential BP ND was calculated using linear graphical analysis with the cerebellum as reference region. The binding of [(11)C]AZD2184 in total grey matter was generally low in the declining group, whereas some binding could be observed in the stable group. Mean BP ND was significantly higher in the stable group compared to the declining group (p = 0.019). An observation was that the three subjects with the highest BP ND were ApoE ε4 allele carriers. We conclude that cognitive decline in the general population does not seem to stand by itself as an early predictor for amyloid deposits.
Purpose Cognitive decline has been suggested as an early marker for later onset of Alzheimer’s disease. We therefore explored the relationship between decline in episodic memory and β-amyloid using positron emission tomography (PET) and [ 11 C]AZD2184, a radioligand with potential to detect low levels of amyloid deposits. Methods Healthy elderly subjects with declining (n = 10) or stable (n = 10) episodic memory over 15 years were recruited from the population-based Betula study and examined with PET. Brain radioactivity was measured after intravenous administration of [ 11 C]AZD2184. The binding potential BP ND was calculated using linear graphical analysis with the cerebellum as reference region. Results The binding of [ 11 C]AZD2184 in total grey matter was generally low in the declining group, whereas some binding could be observed in the stable group. Mean BP ND was significantly higher in the stable group compared to the declining group (p = 0.019). An observation was that the three subjects with the highest BP ND were ApoE ε4 allele carriers. Conclusions We conclude that cognitive decline in the general population does not seem to stand by itself as an early predictor for amyloid deposits.
Purpose : Cognitive decline has been suggested as an early marker for later onset of Alzheimer's disease. We therefore explored the relationship between decline in episodic memory and β-amyloid using positron emission tomography (PET) and [ 11 C]AZD2184, a radioligand with potential to detect low levels of amyloid deposits. Methods : Healthy elderly subjects with declining (n = 10) or stable (n = 10) episodic memory over 15 years were recruited from the population-based Betula study and examined with PET. Brain radioactivity was measured after intravenous administration of [ 11 C]AZD2184 The binding potential  BP ND was calculated using linear graphical analysis with the cerebellum as reference region. Results : The binding of [ 11 C]AZD2184 in total grey matter was generally low in the declining group, whereas some binding could be observed in the stable group. Mean  BP ND was significantly higher in the stable group compared to the declining group (p = 0.019). An observation was that the three subjects with the highest BPND were ApoE ε4 allele carriers. Conclusions : We conclude that cognitive decline in the general population does not seem to stand by itself as an early predictor for amyloid deposits.
Author Nyberg, Lars
Nilsson, Lars-Göran
Halldin, Christer
Persson, Jonas
Forsberg, Anton
Mattsson, Patrik
Farde, Lars
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CitedBy_id crossref_primary_10_3389_fnagi_2021_704661
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Keywords Cognitive decline
Aging
Amyloid
Positron emission tomography
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SSID ssj0018289
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Snippet Purpose Cognitive decline has been suggested as an early marker for later onset of Alzheimer’s disease. We therefore explored the relationship between decline...
Cognitive decline has been suggested as an early marker for later onset of Alzheimer's disease. We therefore explored the relationship between decline in...
Purpose : Cognitive decline has been suggested as an early marker for later onset of Alzheimer's disease. We therefore explored the relationship between...
Purpose Cognitive decline has been suggested as an early marker for later onset of Alzheimer's disease. We therefore explored the relationship between decline...
Purpose: Cognitive decline has been suggested as an early marker for later onset of Alzheimer's disease. We therefore explored the relationship between decline...
SourceID swepub
pubmed
crossref
springer
SourceType Open Access Repository
Index Database
Enrichment Source
Publisher
StartPage 1507
SubjectTerms Aged
Aging
Aminopyridines - pharmacokinetics
Amyloid
Amyloid beta-Peptides - metabolism
Benzothiazoles - pharmacokinetics
Carbon Radioisotopes - pharmacokinetics
Cardiology
Cognition Disorders - diagnostic imaging
Cognition Disorders - metabolism
Cognitive decline
Female
Humans
Imaging
Male
Medicine
Medicine & Public Health
Memory Disorders - diagnostic imaging
Memory Disorders - metabolism
Memory, Episodic
Middle Aged
Molecular Imaging - methods
Nuclear Medicine
Oncology
Orthopedics
Positron emission tomography
Positron-Emission Tomography - methods
Protein Binding
Radiology
Radiopharmaceuticals - pharmacokinetics
Reproducibility of Results
Sensitivity and Specificity
Short Communication
Title β-Amyloid binding in elderly subjects with declining or stable episodic memory function measured with PET and [11C]AZD2184
URI https://link.springer.com/article/10.1007/s00259-015-3103-9
https://www.ncbi.nlm.nih.gov/pubmed/26115835
https://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-87564
https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-120179
https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-107276
http://kipublications.ki.se/Default.aspx?queryparsed=id:131690353
Volume 42
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