Subjective cognition trajectories, Alzheimer biomarkers, and incident mild cognitive impairment

BACKGROUND: Subjective cognitive decline is common in older adults and may represent an early clinical signal along the Alzheimer's disease continuum. The clinical relevance of longitudinal changes in subjective cognitive decline remains unclear. OBJECTIVES: To determine whether trajectories of self- or study partner-reported cognitive decline predict progression to mild cognitive impairment and reflect Alzheimer's disease-specific biological patterns. DESIGN, SETTING, PARTICIPANTS: Data were pooled from two observational cohorts. Cognitively unimpaired participants with baseline amyloid status, repeated assessments of subjective cognitive decline, and clinical follow-up were included. The study included 770 participants with a median follow-up of 5.0 years (interquartile range 4.0-7.0). MEASUREMENTS: Subjective cognitive decline was assessed using the Everyday Cognition questionnaire completed by participants and study partners. Linear mixed-effects models examined associations with amyloid status and progression to mild cognitive impairment. Cox proportional hazards models tested whether one-year changes predicted progression. RESULTS: Amyloid-positive participants and those who progressed to mild cognitive impairment showed steeper increases in self- and study partner-reported cognitive difficulties over time. Among amyloid-positive participants, only increases in study partner-report differentiated progressors from non-progressors. One-year increases in study partner-report predicted a higher risk of mild cognitive impairment compared with unchanged scores (hazard ratio 3.24; 95% confidence interval 1.73-6.07]), with effects confined to amyloid-positive participants. CONCLUSIONS: Short-term increases in study partner-reported cognitive difficulties identify amyloid-positive cognitively unimpaired older adults at increased risk of near-term progression to mild cognitive impairment. Longitudinal monitoring using study partner reports may provide a low-burden and clinically relevant approach for early risk stratification and surveillance in aging populations.

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Publication Details

Journal
The Journal of Prevention of Alzheimer s Disease
Published
2026-05-29
DOI
https://doi.org/10.1016/j.tjpad.2026.100609
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
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article

Subjective cognition trajectories, Alzheimer biomarkers, and incident mild cognitive impairment

Ayda Rostamzadeh, Lukas Preis, Sandra Roeske, Luca Kleineidam et al.
The Journal of Prevention of Alzheimer s Disease
Dementia and Cognitive Impairment Research
article

Subjective cognition trajectories, Alzheimer biomarkers, and incident mild cognitive impairment

Ayda Rostamzadeh, Lukas Preis, Sandra Roeske, Luca Kleineidam, Daria Gref, Melina Stark, Sebastian Sodenkamp, Sophia Stöcklein, Eike Jakob Spruth, Enise Incesoy, Marie Theres Kronmüller, Elizabeth Kuhn, Claudia Bartels, Katharina Buerger, Wenzel Glanz, Annika Spottke, Jens Wiltfang, Alfredo Ramirez, Maria Gemenetzi, Matthis Synofzik, Oliver Peters, Anja Schneider, Matthias C. Schmid, Robert Perneczky, Frederic Brosseron, Klaus Fliessbach, Boris-Stephan Rauchmann, Michael Wagner, Daniel Janowitz, Julian Hellmann-Regen, Josef Priller, Christoph Laske, Ingo Kilimann, Frank Jessen, Niels Hansen, Emrah Düzel, Stefan J. Teipel
article en

Abstract

BACKGROUND: Subjective cognitive decline is common in older adults and may represent an early clinical signal along the Alzheimer's disease continuum. The clinical relevance of longitudinal changes in subjective cognitive decline remains unclear. OBJECTIVES: To determine whether trajectories of self- or study partner-reported cognitive decline predict progression to mild cognitive impairment and reflect Alzheimer's disease-specific biological patterns. DESIGN, SETTING, PARTICIPANTS: Data were pooled from two observational cohorts. Cognitively unimpaired participants with baseline amyloid status, repeated assessments of subjective cognitive decline, and clinical follow-up were included. The study included 770 participants with a median follow-up of 5.0 years (interquartile range 4.0-7.0). MEASUREMENTS: Subjective cognitive decline was assessed using the Everyday Cognition questionnaire completed by participants and study partners. Linear mixed-effects models examined associations with amyloid status and progression to mild cognitive impairment. Cox proportional hazards models tested whether one-year changes predicted progression. RESULTS: Amyloid-positive participants and those who progressed to mild cognitive impairment showed steeper increases in self- and study partner-reported cognitive difficulties over time. Among amyloid-positive participants, only increases in study partner-report differentiated progressors from non-progressors. One-year increases in study partner-report predicted a higher risk of mild cognitive impairment compared with unchanged scores (hazard ratio 3.24; 95% confidence interval 1.73-6.07]), with effects confined to amyloid-positive participants. CONCLUSIONS: Short-term increases in study partner-reported cognitive difficulties identify amyloid-positive cognitively unimpaired older adults at increased risk of near-term progression to mild cognitive impairment. Longitudinal monitoring using study partner reports may provide a low-burden and clinically relevant approach for early risk stratification and surveillance in aging populations.

The Journal of Prevention of Alzheimer s DiseaseVol. 13(8)
University Hospital Bonn (DE), German Center for Neurodegenerative Diseases (DE), Rostocker Zentrum zur Erforschung des Demografischen Wandels (DE), Munich Cluster for Systems Neurology (DE), Nephrologisches Zentrum Goettingen (DE), Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (DE), Hertie Institute for Clinical Brain Research (DE), University Hospital Cologne (DE), University of Rostock (DE), University of Göttingen (DE), Charité - Universitätsmedizin Berlin (DE), University of Tübingen (DE), Ludwig-Maximilians-Universität München (DE), University of Sheffield (GB)
Openalex Percentile: Top 6%
Dementia and Cognitive Impairment Research
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