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@ARTICLE{Altomare:916865,
      author       = {Altomare, Daniele and Collij, Lyduine and Caprioglio,
                      Camilla and Scheltens, Philip and van Berckel, Bart N. M.
                      and Alves, Isadora Lopes and Berkhof, Johannes and de Gier,
                      Yvonne and Garibotto, Valentina and Moro, Christian and
                      Poitrine, Léa and Delrieu, Julien and Payoux, Pierre and
                      Saint-Aubert, Laure and Molinuevo, José Luis and
                      Grau-Rivera, Oriol and Gispert, Juan-Domingo and
                      Minguillón, Carolina and Fauria, Karine and Sanchez, Marta
                      Felez and Rădoi, Andreea and Drzezga, Alexander and Jessen,
                      Frank and Escher, Claus and Zeyen, Philip and Nordberg,
                      Agneta and Savitcheva, Irina and Jelic, Vesna and Walker,
                      Zuzana and Lee, Ho-Yun and Lee, Lean and Demonet,
                      Jean-François and Plaza Wuthrich, Sonia and Gismondi,
                      Rossella and Farrar, Gill and Barkhof, Frederik and
                      Stephens, Andrew W. and Frisoni, Giovanni B. and Consortium,
                      AMYPAD},
      title        = {{D}escription of a {E}uropean memory clinic cohort
                      undergoing amyloid‐{PET}: {T}he {AMYPAD} {D}iagnostic and
                      {P}atient {M}anagement {S}tudy},
      journal      = {Alzheimer's and dementia},
      volume       = {19},
      number       = {3},
      issn         = {1552-5260},
      address      = {Hoboken, NJ},
      publisher    = {Wiley},
      reportid     = {FZJ-2023-00157},
      pages        = {844-856},
      year         = {2023},
      abstract     = {Introduction: AMYPAD Diagnostic and Patient Management
                      Study (DPMS) aims to investigate the clinical utility and
                      cost-effectiveness of amyloid-PET in Europe. Here we present
                      participants' baseline features and discuss the
                      representativeness of the cohort.Methods: Participants with
                      subjective cognitive decline plus (SCD+), mild cognitive
                      impairment (MCI), or dementia were recruited in eight
                      European memory clinics from April 16, 2018, to October 30,
                      2020, and randomized into three arms: ARM1, early
                      amyloid-PET; ARM2, late amyloid-PET; and ARM3,
                      free-choice.Results: A total of 840 participants (244 SCD+,
                      341 MCI, and 255 dementia) were enrolled.
                      Sociodemographic/clinical features did not differ
                      significantly among recruiting memory clinics or with
                      previously reported cohorts. The randomization assigned
                      $35\%$ of participants to ARM1, $32\%$ to ARM2, and $33\%$
                      to ARM3; cognitive stages were distributed equally across
                      the arms.Discussion: The features of AMYPAD-DPMS
                      participants are as expected for a memory clinic population.
                      This ensures the generalizability of future study
                      results.Keywords: Alzheimer's; PET; amyloid; dementia;
                      memory clinic population; mild cognitive impairment;
                      subjective cognitive decline.},
      cin          = {INM-2},
      ddc          = {610},
      cid          = {I:(DE-Juel1)INM-2-20090406},
      pnm          = {5252 - Brain Dysfunction and Plasticity (POF4-525) / 5253 -
                      Neuroimaging (POF4-525)},
      pid          = {G:(DE-HGF)POF4-5252 / G:(DE-HGF)POF4-5253},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {35715930},
      UT           = {WOS:000812481000001},
      doi          = {10.1002/alz.12696},
      url          = {https://juser.fz-juelich.de/record/916865},
}