Clinical impact of [18F]flutemetamol PET among memory clinic patients with an unclear diagnosis.

Purpose: To investigate the impact of amyloid PET with [18F]flutemetamol on diagnosis and treatment management in a cohort of patients attending a tertiary memory clinic in whom, despite extensive cognitive assessment including neuropsychological testing, structural imaging, CSF biomarker analysis a...

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Publicado en:European Journal of Nuclear Medicine & Molecular Imaging Vol. 46; no. 6; pp. 1276 - 1287
Autores principales: Leuzy, Antoine, Savitcheva, Irina, Chiotis, Konstantinos, Lilja, Johan, Andersen, Pia, Bogdanovic, Nenad, Jelic, Vesna, Nordberg, Agneta
Formato: Journal Article
Publicado: Springer Nature Jun2019
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jun2019
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      pub: Springer Nature
      place: New York, New York
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        136129983
        10.1007/s00259-019-04297-5
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        atl: Clinical impact of [18F]flutemetamol PET among memory clinic patients with an unclear diagnosis.
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          Leuzy, Antoine
          Savitcheva, Irina
          Chiotis, Konstantinos
          Lilja, Johan
          Andersen, Pia
          Bogdanovic, Nenad
          Jelic, Vesna
          Nordberg, Agneta
        affil: Department of Neurobiology, Care Sciences and Society, Division of Clinical Geriatrics Center for Alzheimer Research, Karolinska Institutet, Neo, 7th floor, 141 83, Huddinge, Sweden
      sug:
      ab: Purpose: To investigate the impact of amyloid PET with [18F]flutemetamol on diagnosis and treatment management in a cohort of patients attending a tertiary memory clinic in whom, despite extensive cognitive assessment including neuropsychological testing, structural imaging, CSF biomarker analysis and in some cases [18F]FDG PET, the diagnosis remained unclear. Methods: The study population consisted of 207 patients with a clinical diagnosis prior to [18F]flutemetamol PET including mild cognitive impairment (MCI; n = 131), Alzheimer's disease (AD; n = 41), non-AD (n = 10), dementia not otherwise specified (dementia NOS; n = 20) and subjective cognitive decline (SCD; n = 5). Results: Amyloid positivity was found in 53% of MCI, 68% of AD, 20% of non-AD, 20% of dementia NOS, and 60% of SCD patients. [18F]Flutemetamol PET led, overall, to a change in diagnosis in 92 of the 207 patients (44%). A high percentage of patients with a change in diagnosis was observed in the MCI group (n = 67, 51%) and in the dementia NOS group (n = 11; 55%), followed by the non-AD and AD (30% and 20%, respectively). A significant increase in cholinesterase inhibitor treatment was observed after [18F]flutemetamol PET (+218%, 34 patients before and 108 patients after). Conclusion: The present study lends support to the clinical value of amyloid PET in patients with an uncertain diagnosis in the tertiary memory clinic setting.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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