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.