SMAS: Structural MRI-Based AD Score using Bayesian VAE

Nemali, A.; Bernal, J.; Yakupov, R.; Singh, D.; Dyrba, M.; Incesoy, E.; Mukherjee, S.; Peters, O.; Hellmann, J.; Ersoezlue, E.; Preis, L.; Priller, J.; Spruth, E.; Altenstein, S.; Lohse, A.; Schneider, A.; Fliessbach, K.; Kimmich, O.; Wiltfang, J.; Hansen, N.; Schott, B.; Rostamzadeh, A.; Glanz, W.; Butryn, M.; Buerger, K.; Janowitz, D.; Ewers, M.; Perneczky, R.; Rauchmann, B.; Teipel, S.; Kilimann, I.; Goerss, D.; Laske, C.; Sodenkamp, S.; Spottke, A.; Coenjaerts, M.; Brosseron, F.; Luesebrink, F.; Dechent, P.; Scheffler, K.; Hetzer, S.; Kleineidam, L.; Stark, M.; Jessen, F.; Duezel, E.; Zieg

doi:10.1101/2024.11.07.622411

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bioRxiv · 10.1101/2024.11.07.622411

SMAS: Structural MRI-Based AD Score using Bayesian VAE

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Abstract

This study introduces the Structural MRI-based Alzheimers Disease Score (SMAS), a novel index intended to quantify Alzheimers Disease (AD)-related morphometric patterns using a deep learning Bayesian-supervised Variational Autoencoder (Bayesian-SVAE). SMAS index was constructed using baseline structural MRI data from the DELCODE study and evaluated longitudinally in two independent cohorts: DEL-CODE (n=415) and ADNI (n=190). Our findings indicate that SMAS has strong associations with cognitive performance (DELCODE: r=-0.83; ADNI: r=-0.62), age (DEL-CODE: r=0.50; ADNI: r=0.28), hippocampal volume (DEL-CODE: r=-0.44; ADNI: r=-0.66), and total grey matter volume (DELCODE: r=-0.42; ADNI: r=-0.47), suggesting its potential as a biomarker for AD-related brain atrophy. Moreover, our longitudinal studies suggest that SMAS may be useful for early identification and tracking of AD. The model demonstrated significant predictive accuracy in distinguishing cognitively healthy individuals from those with AD (DELCODE: AUC=0.971 at baseline, 0.833 at 36 months; ADNI: AUC=0.817 at baseline, improving to 0.903 at 24 months). Notably, over a 36-month period, SMAS index outperformed existing measures such as SPARE-AD and hippocampal volume. Relevance map analysis revealed significant morphological changes in key AD-related brain regions--including the hippocampus, posterior cingulate cortex, precuneus, and lateral parietal cortex--highlighting that SMAS is a sensitive and interpretable biomarker of brain atrophy, suitable for early AD detection and longitudinal monitoring of disease progression.

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Nemali, A., Bernal, J., Yakupov, R., Singh, D., Dyrba, M., Incesoy, E., Mukherjee, S., Peters, O., Hellmann, J., Ersoezlue, E., Preis, L., Priller, J., Spruth, E., Altenstein, S., Lohse, A., Schneider, A., Fliessbach, K., Kimmich, O., Wiltfang, J., Hansen, N., Schott, B., Rostamzadeh, A., Glanz, W., Butryn, M., Buerger, K., Janowitz, D., Ewers, M., Perneczky, R., Rauchmann, B., Teipel, S., Kilimann, I., Goerss, D., Laske, C., Sodenkamp, S., Spottke, A., Coenjaerts, M., Brosseron, F., Luesebrink, F., Dechent, P., Scheffler, K., Hetzer, S., Kleineidam, L., Stark, M., Jessen, F., Duezel, E., Zieg. 2024-11-07. SMAS: Structural MRI-Based AD Score using Bayesian VAE. https://doi.org/10.1101/2024.11.07.622411

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