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Minor neuropsychological deficits and stage 2 of Alzheimer's disease

Authors

  • Melina Stark
  • Michael Wagner
  • Elizabeth Kuhn
  • Sandra Roeske
  • Holger Amthauer
  • Claudia Bartels
  • Henning Boecker
  • Frederic Brosseron
  • Ralph Buchert
  • Katharina Buerger
  • Marcel Daamen
  • Alexander Drzezga
  • Emrah Düzel
  • Ersin Ersözlü
  • Markus Essler
  • Michael Ewers
  • Klaus Fliessbach
  • Wenzel Glanz
  • Julian Hellmann-Regen
  • Enise I. Incesoy
  • Daniel Janowitz
  • Konstantinia Kafali
  • Ingo Kilimann
  • Bernd Joachim Krause
  • Marie Kronmüller
  • Christoph Laske
  • Franziska Maier
  • Angelika Maurer
  • Jochen Michely
  • Robert Perneczky
  • Oliver Peters
  • Lukas Preis
  • Josef Priller
  • Boris-Stephan Rauchmann
  • Matthias Reimold
  • Axel Rominger
  • Matthias Schmid
  • Anja Schneider
  • Sebastian Sodenkamp
  • Annika Spottke
  • Eike Jakob Spruth
  • Stefan Teipel
  • Jens Wiltfang
  • Frank Jessen
  • Luca Kleineidam

Journal

  • Alzheimer's & Dementia

Citation

  • Alzheimers Dement 22 (5): e71458

Abstract

  • INTRODUCTION: Subtle symptoms, like subjective cognitive decline (SCD) and minor neuropsychological deficits (MNPD), can improve the risk stratification in preclinical Alzheimer´s disease (AD) but their importance is insufficiently elaborated. METHODS: We pooled data from cognitively normal individuals participating in three longitudinal cohort studies (N = 13,192, 8,359[63.3%] female, mean [SD] age 71.0[8.4]). RESULTS: Compared to participants without SCD and MNPD (SCD-/MNPD-), SCD-/MNPD+, SCD+/MNPD-, and SCD+/MNPD+ participants had an increased risk for mild cognitive impairment (MCI) and dementia, including in amyloid-positive individuals. Focusing on SCD+/MNPD+ participants triples the positive predictive value of amyloid biomarker testing for the 5-year prediction of MCI and reduces the required samples size for trials in preclinical AD to one fourth, compared to considering all cognitively normal participants regardless of subtle symptoms. DISCUSSION: SCD and MNPD offer a powerful approach for risk stratification in preclinical AD, which can improve clinical trial designs, risk counseling, and future case identifications for early treatment.


DOI

doi:10.1002/alz.71458