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Search: WFRF:(Chiotis Konstantinos) > Imaging in-vivo tau...

Imaging in-vivo tau pathology in Alzheimer's disease with THK5317 PET in a multimodal paradigm

Chiotis, Konstantinos (author)
Karolinska Institutet
Saint-Aubert, Laure (author)
Karolinska Institutet
Savitcheva, Irina (author)
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Jelic, Vesna (author)
Karolinska Institutet
Andersen, Pia (author)
Jonasson, My (author)
Uppsala universitet,Radiologi
Eriksson, Jonas (author)
Uppsala universitet,Avdelningen för Molekylär Avbildning
Lubberink, Mark (author)
Uppsala universitet,Radiologi
Almkvist, Ove (author)
Stockholms universitet,Biologisk psykologi,Karolinska Institutet, Sweden; Karolinska University Hospital, Sweden
Wall, Anders (author)
Uppsala universitet,Radiologi
Antoni, Gunnar (author)
Uppsala universitet,Avdelningen för Molekylär Avbildning
Nordberg, Agneta (author)
Karolinska Institutet
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 (creator_code:org_t)
2016-03-21
2016
English.
In: European Journal of Nuclear Medicine and Molecular Imaging. - : Springer Science and Business Media LLC. - 1619-7070 .- 1619-7089. ; 43:9, s. 1686-1699
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Purpose The aim of this study was to explore the cerebral distribution of the tau-specific PET tracer [F-18]THK5317 (also known as (S)-[F-18]THK5117) retention in different stages of Alzheimer's disease; and study any associations with markers of hypometabolism and amyloid-beta deposition. Methods Thirty-three individuals were enrolled, including nine patients with Alzheimer's disease dementia, thirteen with mild cognitive impairment (MCI), two with non-Alzheimer's disease dementia, and nine healthy controls (five young and four elderly). In a multi-tracer PET design [F-18]THK5317, [C-11] Pittsburgh compound B ([C-11]PIB), and [F-18]FDG were used to assess tau pathology, amyloid-beta deposition and cerebral glucose metabolism, respectively. The MCI patients were further divided into MCI [C-11]PIB-positive (n=11) and MCI [C-11]PIB-negative (n=2) groups. Results Test-retest variability for [F-18]THK5317-PET was very low (1.17-3.81 %), as shown by retesting five patients. The patients with prodromal (MCI [C-11]PIB-positive) and dementia-stage Alzheimer's disease had significantly higher [F-18]THK5317 retention than healthy controls (p=0.002 and p=0.001, respectively) in areas exceeding limbic regions, and their discrimination from this control group (using the area under the curve) was >98 %. Focal negative correlations between [F-18]THK5317 retention and [F-18]FDG uptake were observed mainly in the frontal cortex, and focal positive correlations were found between [F-18]THK5317 and [C-11] PIB retentions isocortically. One patient with corticobasal degeneration syndrome and one with progressive supranuclear palsy showed no [C-11]PIB but high [F-18]THK5317 retentions with a different regional distribution from that in Alzheimer's disease patients. Conclusions The tau-specific PET tracer [F-18]THK5317 images in vivo the expected regional distribution of tau pathology. This distribution contrasts with the different patterns of hypometabolism and amyloid-beta deposition.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Geriatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Geriatrics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Radiologi och bildbehandling (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Radiology, Nuclear Medicine and Medical Imaging (hsv//eng)

Keyword

Positron emission tomography
Alzheimer's disease
Tau
Neurofibrillary tangles
THK5317
Other dementia
Non-AD
Amyloid PET
FDG
PIB
Psychology
psykologi

Publication and Content Type

ref (subject category)
art (subject category)

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