Subtyping and staging of Alzheimer’s disease from routine structural MRI with PHASE–AD
Authors
- Hannah Baumeister
- Falk Lüsebrink
- Luca Kleineidam
- Niels Hansen
- Matthias Schmid
- Alexis Moscoso
- Antoine Leuzy
- Sophie E. Mastenbroek
- Colin Groot
- Frederic Brosseron
- Alfredo Ramirez
- Lukas Preis
- Daria Gref
- Eike J. Spruth
- Maria Gemenetzi
- Slawek Altenstein
- Klaus Fliessbach
- Okka Kimmich
- Björn H. Schott
- Ayda Rostamzadeh
- Wenzel Glanz
- Enise I. Incesoy
- Michaela Butryn
- Daniel Janowitz
- Boris-Stephan Rauchmann
- Mihovil Mladinov
- Alice Grazia
- Sebastian Sodenkamp
- Tony Stöcker
- Stefan Hetzer
- Peter Dechent
- Sophia Stoecklein
- Oliver Peters
- Julian Hellmann-Regen
- Josef Priller
- Anja Schneider
- Jens Wiltfang
- Katharina Buerger
- Robert Perneczky
- Stefan Teipel
- Christoph Laske
- Annika Spottke
- Michael Wagner
- Frank Jessen
- Emrah Düzel
- David Berron
Journal
- medRxiv
Citation
- medRxiv
Abstract
Structural MRI is routinely acquired in the clinical assessment of Alzheimer’s disease, yet quantitative morphometric indices derived from these scans remain largely confined to research settings. Here we present PHASE–AD — a framework that translates such indices into clinically interpretable classifications of atrophy subtype and stage that jointly capture atrophy progression while accounting for inter-individual atrophy heterogeneity. PHASE–AD is trained on MRI scans from 8,415 participants and robustly captures limbic-predominant and hippocampal-sparing atrophy subtypes that were identified across seven independent datasets. Two cross-validation schemes revealed high robustness across different field strength and scanner manufacturer configurations. Atrophy classifications were associated with diverging clinical profiles and tau accumulation patterns. In prospective designs mirroring contemporary AD trials, they stratified longitudinal cognitive trajectories and outperformed semi-quantitative visual MRI assessments as a clinically established comparator. These findings support the integration of automated atrophy subtyping and staging into clinical practice and pharmacological trials.