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Change in brain amyloid load and cognition in patients with amnestic mild cognitive impairment : a 3-year follow-up study

Rauhala, Elina (författare)
Clinical Neurosciences, Faculty of Medicine, Turku University Hospital, University of Turku and Neurocenter, Turku, Finland
Johansson, Jarkko (författare)
Umeå universitet,Diagnostisk radiologi,Turku PET Centre, Turku University Hospital, Turku, Finland
Karrasch, Mira (författare)
Department of Psychology, Åbo Akademi University, Turku, Finland
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Eskola, Olli (författare)
Turku PET Centre, University of Turku, Turku, Finland
Tolvanen, Tuula (författare)
Turku PET Centre, University of Turku, Turku, Finland; Department of Medical Physics, Turku University Hospital, Turku, Finland
Parkkola, Riitta (författare)
Department of Radiology, University of Turku and Turku University Hospital, Turku, Finland
Virtanen, Kirsi A. (författare)
Turku PET Centre, Turku University Hospital, Turku, Finland
Rinne, Juha O. (författare)
Turku PET Centre, Turku University Hospital, Turku, Finland; InFLAMES Research Flagship Center, University of Turku, Turku, Finland
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 (creator_code:org_t)
2022-09-05
2022
Engelska.
Ingår i: EJNMMI Research. - : Springer. - 2191-219X. ; 12:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Our aim was to investigate the discriminative value of 18F-Flutemetamol PET in longitudinal assessment of amyloid beta accumulation in amnestic mild cognitive impairment (aMCI) patients, in relation to longitudinal cognitive changes.Methods: We investigated the change in 18F-Flutemetamol uptake and cognitive impairment in aMCI patients over time up to 3 years which enabled us to investigate possible association between changes in brain amyloid load and cognition over time. Thirty-four patients with aMCI (mean age 73.4 years, SD 6.6) were examined with 18F-Flutemetamol PET scan, brain MRI and cognitive tests at baseline and after 3-year follow-up or earlier if the patient had converted to Alzheimer´s disease (AD). 18F-Flutemetamol data were analyzed both with automated region-of-interest analysis and voxel-based statistical parametric mapping.Results: 18F-flutemetamol uptake increased during the follow-up, and the increase was significantly higher in patients who were amyloid positive at baseline as compared to the amyloid-negative ones. At follow-up, there was a significant association between 18F-Flutemetamol uptake and MMSE, logical memory I (immediate recall), logical memory II (delayed recall) and verbal fluency. An association was seen between the increase in 18F-Flutemetamol uptake and decline in MMSE and logical memory I scores.Conclusions: In the early phase of aMCI, presence of amyloid pathology at baseline strongly predicted amyloid accumulation during follow-up, which was further paralleled by cognitive declines. Inversely, some of our patients remained amyloid negative also at the end of the study without significant change in 18F-Flutemetamol uptake or cognition. Future studies with longer follow-up are needed to distinguish whether the underlying pathophysiology of aMCI in such patients is other than AD.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (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)

Nyckelord

Alzheimer
Amyloid PET
Cognition
Flutemetamol
Follow-up
Mild cognitive impairment
Positron emission tomography

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