PET imaging of amyloid deposition in patients with mild cognitive impairment

It is of great clinical value to identify subjects at a high risk of developing AD. We previously found that the amyloid positron emission tomography (PET) tracer PIB showed a robust difference in retention in the brain between AD patients and healthy controls (HC). Twenty-one patients diagnosed wit...

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Published inNeurobiology of aging Vol. 29; no. 10; pp. 1456 - 1465
Main Authors Forsberg, Anton, Engler, Henry, Almkvist, Ove, Blomquist, Gunnar, Hagman, Göran, Wall, Anders, Ringheim, Anna, Långström, Bengt, Nordberg, Agneta
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.10.2008
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Abstract It is of great clinical value to identify subjects at a high risk of developing AD. We previously found that the amyloid positron emission tomography (PET) tracer PIB showed a robust difference in retention in the brain between AD patients and healthy controls (HC). Twenty-one patients diagnosed with MCI (mean age 63.3 ± 7.8 (S.D.) years) underwent PET studies with 11C-PIB, and 18F-fluoro-deoxy-glucose (FDG) to measure cerebral glucose metabolism, as well as assessment of cognitive function and CSF sampling. Reference group data from 27 AD patients and 6 healthy controls, respectively, were used for comparison. The mean cortical PIB retention for the MCI patients was intermediate compared to HC and AD. Seven MCI patients that later at clinical follow-up converted to AD (8.1 ± 6.0 (S.D.) months) showed significant higher PIB retention compared to non-converting MCI patients and HC, respectively ( ps < 0.01). The PIB retention in MCI converters was comparable to AD patients ( p > 0.01). Correlations were observed in the MCI patients between PIB retention and CSF Aβ 1-42, total Tau and episodic memory, respectively.
AbstractList It is of great clinical value to identify subjects at a high risk of developing AD. We previously found that the amyloid positron emission tomography (PET) tracer PIB showed a robust difference in retention in the brain between AD patients and healthy controls (HC). Twenty-one patients diagnosed with MCI (mean age 63.3 ± 7.8 (S.D.) years) underwent PET studies with 11C-PIB, and 18F-fluoro-deoxy-glucose (FDG) to measure cerebral glucose metabolism, as well as assessment of cognitive function and CSF sampling. Reference group data from 27 AD patients and 6 healthy controls, respectively, were used for comparison. The mean cortical PIB retention for the MCI patients was intermediate compared to HC and AD. Seven MCI patients that later at clinical follow-up converted to AD (8.1 ± 6.0 (S.D.) months) showed significant higher PIB retention compared to non-converting MCI patients and HC, respectively ( ps < 0.01). The PIB retention in MCI converters was comparable to AD patients ( p > 0.01). Correlations were observed in the MCI patients between PIB retention and CSF Aβ 1-42, total Tau and episodic memory, respectively.
It is of great clinical value to identify subjects at a high risk of developing AD. We previously found that the amyloid positron emission tomography (PET) tracer PIB showed a robust difference in retention in the brain between AD patients and healthy controls (HC). Twenty-one patients diagnosed with MCI (mean age 63.3+/-7.8 (S.D.) years) underwent PET studies with (11)C-PIB, and (18)F-fluoro-deoxy-glucose (FDG) to measure cerebral glucose metabolism, as well as assessment of cognitive function and CSF sampling. Reference group data from 27 AD patients and 6 healthy controls, respectively, were used for comparison. The mean cortical PIB retention for the MCI patients was intermediate compared to HC and AD. Seven MCI patients that later at clinical follow-up converted to AD (8.1+/-6.0 (S.D.) months) showed significant higher PIB retention compared to non-converting MCI patients and HC, respectively (ps<0.01). The PIB retention in MCI converters was comparable to AD patients (p>0.01). Correlations were observed in the MCI patients between PIB retention and CSF Abeta(1-42), total Tau and episodic memory, respectively.
mild cognitive impairment, converters, amyloid, PET, PIB, FDG, CSF biomarkers/k It is of great clinical value to identify Subjects at a high risk of developing AD. We previously found that the amyloid positron emission tomography (PET) tracer PIB showed a robust difference in retention in the brain between AD patients and healthy controls (HC). Twenty-one patients diagnosed with MCI (mean age 63.3 +/- 7.8 (S.D.) years) Underwent PET Studies with C-11-PIB, and F-18-fluoro-deoxy-glucose (FDG) to measure cerebral glucose metabolism, its well as assessment of cognitive function and CSF sampling. Reference group data from 27 AD patients and 6 healthy controls, respectively. were Used for comparison. The mean cortical PIB retention for the MCI patients was intermediate compared to HC and AD. Seven MCI patients that later Lit clinical follow-up converted to AD (8.1 +/- 6.0 (S.D.) months) showed significant higher PI B retention compared to non-converting MCI patients and HC, respcctively (ps &lt; , 0.01). The PIB retention in MCI converters was comparable to AD patients (p &gt; , 0.01). Correlations were observed in the MCI patients between PI B retention and CSF A beta(1-42). total Tau and episodic memory, respectively.
It is of great clinical value to identify subjects at a high risk of developing AD. We previously found that the amyloid positron emission tomography (PET) tracer PIB showed a robust difference in retention in the brain between AD patients and healthy controls (HC). Twenty-one patients diagnosed with MCI (mean age 63.3+/-7.8 (S.D.) years) underwent PET studies with (11)C-PIB, and (18)F-fluoro-deoxy-glucose (FDG) to measure cerebral glucose metabolism, as well as assessment of cognitive function and CSF sampling. Reference group data from 27 AD patients and 6 healthy controls, respectively, were used for comparison. The mean cortical PIB retention for the MCI patients was intermediate compared to HC and AD. Seven MCI patients that later at clinical follow-up converted to AD (8.1+/-6.0 (S.D.) months) showed significant higher PIB retention compared to non-converting MCI patients and HC, respectively (ps<0.01). The PIB retention in MCI converters was comparable to AD patients (p>0.01). Correlations were observed in the MCI patients between PIB retention and CSF Abeta(1-42), total Tau and episodic memory, respectively.It is of great clinical value to identify subjects at a high risk of developing AD. We previously found that the amyloid positron emission tomography (PET) tracer PIB showed a robust difference in retention in the brain between AD patients and healthy controls (HC). Twenty-one patients diagnosed with MCI (mean age 63.3+/-7.8 (S.D.) years) underwent PET studies with (11)C-PIB, and (18)F-fluoro-deoxy-glucose (FDG) to measure cerebral glucose metabolism, as well as assessment of cognitive function and CSF sampling. Reference group data from 27 AD patients and 6 healthy controls, respectively, were used for comparison. The mean cortical PIB retention for the MCI patients was intermediate compared to HC and AD. Seven MCI patients that later at clinical follow-up converted to AD (8.1+/-6.0 (S.D.) months) showed significant higher PIB retention compared to non-converting MCI patients and HC, respectively (ps<0.01). The PIB retention in MCI converters was comparable to AD patients (p>0.01). Correlations were observed in the MCI patients between PIB retention and CSF Abeta(1-42), total Tau and episodic memory, respectively.
Abstract It is of great clinical value to identify subjects at a high risk of developing AD. We previously found that the amyloid positron emission tomography (PET) tracer PIB showed a robust difference in retention in the brain between AD patients and healthy controls (HC). Twenty-one patients diagnosed with MCI (mean age 63.3 ± 7.8 (S.D.) years) underwent PET studies with11 C-PIB, and18 F-fluoro-deoxy-glucose (FDG) to measure cerebral glucose metabolism, as well as assessment of cognitive function and CSF sampling. Reference group data from 27 AD patients and 6 healthy controls, respectively, were used for comparison. The mean cortical PIB retention for the MCI patients was intermediate compared to HC and AD. Seven MCI patients that later at clinical follow-up converted to AD (8.1 ± 6.0 (S.D.) months) showed significant higher PIB retention compared to non-converting MCI patients and HC, respectively ( p s < 0.01). The PIB retention in MCI converters was comparable to AD patients ( p > 0.01). Correlations were observed in the MCI patients between PIB retention and CSF Aβ1-42 , total Tau and episodic memory, respectively.
It is of great clinical value to identify subjects at a high risk of developing AD. We previously found that the amyloid positron emission tomography (PET) tracer PIB showed a robust difference in retention in the brain between AD patients and healthy controls (HC). Twenty-one patients diagnosed with MCI (mean age 63.3 ± 7.8 (S.D.) years) underwent PET studies with 11C-PIB, and 18F-fluoro-deoxy-glucose (FDG) to measure cerebral glucose metabolism, as well as assessment of cognitive function and CSF sampling. Reference group data from 27 AD patients and 6 healthy controls, respectively, were used for comparison. The mean cortical PIB retention for the MCI patients was intermediate compared to HC and AD. Seven MCI patients that later at clinical follow-up converted to AD (8.1 ± 6.0 (S.D.) months) showed significant higher PIB retention compared to non-converting MCI patients and HC, respectively (ps &lt; 0.01). The PIB retention in MCI converters was comparable to AD patients (p &gt; 0.01). Correlations were observed in the MCI patients between PIB retention and CSF Aβ1-42, total Tau and episodic memory, respectively.
Author Långström, Bengt
Blomquist, Gunnar
Almkvist, Ove
Ringheim, Anna
Engler, Henry
Hagman, Göran
Wall, Anders
Forsberg, Anton
Nordberg, Agneta
Author_xml – sequence: 1
  givenname: Anton
  surname: Forsberg
  fullname: Forsberg, Anton
  organization: Karolinska Institute, Department of Neurobiology, Care Sciences and Society, Stockholm, Sweden
– sequence: 2
  givenname: Henry
  surname: Engler
  fullname: Engler, Henry
  organization: Department of Nuclear Medicine, Uppsala University Hospital, Uppsala, Sweden
– sequence: 3
  givenname: Ove
  surname: Almkvist
  fullname: Almkvist, Ove
  organization: Karolinska Institute, Department of Neurobiology, Care Sciences and Society, Stockholm, Sweden
– sequence: 4
  givenname: Gunnar
  surname: Blomquist
  fullname: Blomquist, Gunnar
  organization: Department of Oncology, Radiology and Clinical Immunology, Uppsala University, Uppsala, Sweden
– sequence: 5
  givenname: Göran
  surname: Hagman
  fullname: Hagman, Göran
  organization: Department of Geriatric Medicine, Karolinska University Hospital Huddinge, Stockholm, Sweden
– sequence: 6
  givenname: Anders
  surname: Wall
  fullname: Wall, Anders
  organization: Uppsala Imanet AB, Imanet, GE Healthcare, Sweden
– sequence: 7
  givenname: Anna
  surname: Ringheim
  fullname: Ringheim, Anna
  organization: Uppsala Imanet AB, Imanet, GE Healthcare, Sweden
– sequence: 8
  givenname: Bengt
  surname: Långström
  fullname: Långström, Bengt
  organization: Uppsala Imanet AB, Imanet, GE Healthcare, Sweden
– sequence: 9
  givenname: Agneta
  surname: Nordberg
  fullname: Nordberg, Agneta
  email: Agneta.K.Nordberg@ki.se
  organization: Karolinska Institute, Department of Neurobiology, Care Sciences and Society, Stockholm, Sweden
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SSID ssj0007476
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Snippet It is of great clinical value to identify subjects at a high risk of developing AD. We previously found that the amyloid positron emission tomography (PET)...
Abstract It is of great clinical value to identify subjects at a high risk of developing AD. We previously found that the amyloid positron emission tomography...
mild cognitive impairment, converters, amyloid, PET, PIB, FDG, CSF biomarkers/k It is of great clinical value to identify Subjects at a high risk of developing...
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StartPage 1456
SubjectTerms Aged
Aged, 80 and over
Aging - metabolism
Aging - pathology
Alzheimer Disease - diagnostic imaging
Alzheimer Disease - pathology
Alzheimer Disease - physiopathology
Amyloid
Amyloid beta-Peptides - metabolism
Benzothiazoles
Cerebral Cortex - diagnostic imaging
Cerebral Cortex - pathology
Cerebral Cortex - physiopathology
Cognition Disorders - diagnostic imaging
Cognition Disorders - pathology
Cognition Disorders - physiopathology
Converters
CSF biomarkers
Disease Progression
FDG
Female
Fluorodeoxyglucose F18
Glucose - metabolism
Humans
Internal Medicine
Male
MEDICIN
MEDICINE
Middle Aged
Mild cognitive impairment
Neurology
Neuropsychological Tests
PET
PIB
Plaque, Amyloid - diagnostic imaging
Plaque, Amyloid - metabolism
Plaque, Amyloid - pathology
Positron-Emission Tomography
Predictive Value of Tests
Prognosis
Psychology
Psykologi
SAMHÄLLSVETENSKAP
SOCIAL SCIENCES
Socialvetenskap
Title PET imaging of amyloid deposition in patients with mild cognitive impairment
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