Transfer learning for cognitive reserve quantification
•Quantification of cognitive reserve using brain measures for pre-symptomatic Alzheimer's patients can be estimated by leveraging lifespan data.•Multi-center, multi-scanner, multi-sequence can affect the performance of the quantification.•Leveraging lifespan data from a single site can improve...
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Veröffentlicht in: | NeuroImage (Orlando, Fla.) Fla.), 2022-09, Vol.258, p.119353-119353, Article 119353 |
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Zusammenfassung: | •Quantification of cognitive reserve using brain measures for pre-symptomatic Alzheimer's patients can be estimated by leveraging lifespan data.•Multi-center, multi-scanner, multi-sequence can affect the performance of the quantification.•Leveraging lifespan data from a single site can improve the performance.•Transfer learning allows the pre-trained network to successfully reconstruct the dataset acquired from different domains or age groups.
Cognitive reserve (CR) has been introduced to explain individual differences in susceptibility to cognitive or functional impairment in the presence of age or pathology. We developed a deep learning model to quantify the CR as residual variance in memory performance using the Structural Magnetic Resonance Imaging (sMRI) data from a lifespan healthy cohort. The generalizability of the sMRI-based deep learning model was tested in two independent healthy and Alzheimer's cohorts using transfer learning framework.
Structural MRIs were collected from three cohorts: 495 healthy adults (age: 20-80) from RANN, 620 healthy adults (age: 36-100) from lifespan Human Connectome Project Aging (HCPA), and 941 adults (age: 55-92) from Alzheimer's Disease Neuroimaging Initiative (ADNI). Region of interest (ROI)-specific cortical thickness and volume measures were extracted using the Desikan-Killiany Atlas. CR was quantified by residuals which subtract the predicted memory from the true memory. Cascade neural network (CNN) models were used to train RANN dataset for memory prediction. Transfer learning was applied to transfer the T1 imaging-based model from source domain (RANN) to the target domains (HCPA or ADNI).
The CNN model trained on the RANN dataset exhibited strong linear correlation between true and predicted memory based on the T1 cortical thickness and volume predictors. In addition, the model generated from healthy lifespan data (RANN) was able to generalize to an independent healthy lifespan data (HCPA) and older demented participants (ADNI) across different scanner types. The estimated CR was correlated with CR proxies such education and IQ across all three datasets.
The current findings suggest that the transfer learning approach is an effective way to generalize the residual-based CR estimation. It is applicable to various diseases and may flexibly incorporate different imaging modalities such as fMRI and PET, making it a promising tool for scientific and clinical purposes. |
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ISSN: | 1053-8119 1095-9572 |
DOI: | 10.1016/j.neuroimage.2022.119353 |