Predicting Alzheimer's disease progression using deep recurrent neural networks
Minh NguyeniD, Tong HeiD, Lijun AniD, Daniel C. AlexanderiD, Jiashi FengiD, B.T. Thomas YeoiD, for the Alzheimer’s Disease Neuroimaging Initiative
Abstract
Early identification of individuals at risk of developing Alzheimers disease (AD) dementia is important for developing disease-modifying therapies. In this study, given multimodal AD markers and clinical diagnosis of an individual from one or more timepoints, we seek to predict the clinical diagnosis, cognition and ventricular volume of the individual for every month (indefinitely) into the future. We proposed and applied a minimal recurrent neural network (minimalRNN) model to data from The Alzheimers Disease Prediction Of Longitudinal Evolution (TADPOLE) challenge, comprising longitudinal data of 1677 participants (Marinescu et al. 2018) from the Alzheimers Disease Neuroimaging Initiative (ADNI). We compared the performance of the minimalRNN model and four baseline algorithms up to 6 years into the future. Most previous work on predicting AD progression ignore the issue of missing data, which is a prevalent issue in longitudinal data. Here, we explored three different strategies to handle missing data. Two of the strategies treated the missing data as a "preprocessing" issue, by imputing the missing data using the previous timepoint ("forward filling") or linear interpolation ("linear filling). The third strategy utilized the minimalRNN model itself to fill in the missing data both during training and testing ("model filling"). Our analyses suggest that the minimalRNN with "model filling" compared favorably with baseline algorithms, including support vector machine/regression, linear state space (LSS) model, and long short-term memory (LSTM) model. Importantly, although the training procedure utilized longitudinal data, we found that the trained minimalRNN model exhibited similar performance, when using only 1 input timepoint or 4 input timepoints, suggesting that our approach might work well with just cross-sectional data. An earlier version of our approach was ranked 5th (out of 53 entries) in the TADPOLE challenge in 2019. The current approach is ranked 2nd out of 63 entries as of June 3rd, 2020.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 213
- FWCI
- 16.96
- Field percentile
- top 1%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- PPAD: A deep learning architecture to predict progression of Alzheimer's disease
Mohammad Al Olaimat, Jared Martinez, … Alzheimer’s Disease Neuroimaging Initiative·BioinformaticsPeer-reviewed·May 24, 2023
- Deep Residual Learning for Neuroimaging: An application to Predict Progression to Alzheimer’s Disease
Anees Abrol, Manish Bhattarai, … for the Alzheimer’s Disease Neuroimaging Initiative·bioRxiv·Apr 24, 2019
- Predicting Alzheimer's Disease Progression from Sparse Multimodal Data by NeuralODE Models
Andrea Zanin, Stefano Pagani, … the Alzheimer’s Disease Neuroimaging Initiative ADNI·bioRxiv·Aug 26, 2025
- Predicting Alzheimer's disease progression trajectory and clinical subtypes using machine learning
Vipul K. Satone, Rachneet Kaur, … Faraz Faghri·bioRxiv·Aug 26, 2020
- Quantitative longitudinal predictions of Alzheimer's disease by multi-modal predictive learning
Mithilesh Prakash, Mahmoud Abdelaziz, … Alzheimer’s Disease Neuroimaging Initiative·Journal of Alzheimer s DiseasePeer-reviewed·Jan 12, 2021
- Interpretable Deep Temporal Structure Learning Model for Early Detection of Alzheimer's Disease
Xiaoqian Wang, Dinggang G. Shen, Heng Huang·bioRxiv·Dec 12, 2019