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Transcranial Direct Current Stimulation (tDCS) is a non-invasive brain stimulation method that applies neuromodulatory effects to the brain via low-intensity, direct current. It has shown possible positive effects in areas such as depression, substance use disorder, anxiety, and pain. Unfortunately, mixed trial results have delayed the field’s progress. Electrical current field approximation provides a way for tDCS researchers to estimate how an individual will respond to specific tDCS parameters. Publicly available physics-based stimulators have led to much progress; however, they can be error-prone, susceptible to quality issues (e.g., poor segmentation), and take multiple hours to run. Digital functional twins provide a method of estimating brain function in response to stimuli using computational methods. We seek to implement this idea for individualized tDCS. Hence, this work provides a proof-of-concept for generating electrical field maps for tDCS directly from T1-weighted magnetic resonance images (MRIs). Our deep learning method employs special loss regularizations to improve the model’s generalizability and calibration across individual scans and electrode montages. Users may enter a desired electrode montage in addition to the unique MRI for a custom output. Our dataset includes 442 unique individual heads from individuals across the adult lifespan. The pipeline can generate results on the scale of minutes, unlike physics-based systems that can take 1–3 hours. Overall, our methods will help streamline the process of individual current dose estimations for improved tDCS interventions. To support open science, the code that is associated with this paper is available at: https://github.com/lab-smile/tDCS-DT. 

Abstract Whole-head segmentation from Magnetic Resonance Images (MRI) establishes the foundation for individualized computational models using finite element method (FEM). This foundation paves the path for computer-aided solutions in fields such as non-invasive brain stimulation. Most current automatic head segmentation tools are developed using healthy young adults. Thus, they may neglect the older population that is more prone to age-related structural decline such as brain atrophy. In this work, we present a new deep learning method called GRACE, which stands for General, Rapid, And Comprehensive whole-hEad tissue segmentation. GRACE is trained and validated on a novel dataset that consists of 177 manually corrected MR-derived reference segmentations that have undergone meticulous manual review. Each T1-weighted MRI volume is segmented into 11 tissue types, including white matter, grey matter, eyes, cerebrospinal fluid, air, blood vessel, cancellous bone, cortical bone, skin, fat, and muscle. To the best of our knowledge, this work contains the largest manually corrected dataset to date in terms of number of MRIs and segmented tissues. GRACE outperforms five freely available software tools and a traditional 3D U-Net on a five-tissue segmentation task. On this task, GRACE achieves an average Hausdorff Distance of 0.21, which exceeds the runner-up at an average Hausdorff Distance of 0.36. GRACE can segment a whole-head MRI in about 3 seconds, while the fastest software tool takes about 3 minutes. In summary, GRACE segments a spectrum of tissue types from older adults’ T1-MRI scans at favorable accuracy and speed. The trained GRACE model is optimized on older adult heads to enable high-precision modeling in age-related brain disorders. To support open science, the GRACE code and trained weights are made available online and open to the research community at https://github.com/lab-smile/GRACE. 

Background and Objectives: Prediction of decline to dementia using objective biomarkers in high-risk patients with amnestic mild cognitive impairment (aMCI) has immense utility. Our objective was to use multimodal MRI to (1) determine whether accurate and precise prediction of dementia conversion could be achieved using baseline data alone, and (2) generate a map of the brain regions implicated in longitudinal decline to dementia. Methods: Participants meeting criteria for aMCI at baseline ( N = 55) were classified at follow-up as remaining stable/improved in their diagnosis ( N = 41) or declined to dementia ( N = 14). Baseline T1 structural MRI and resting-state fMRI (rsfMRI) were combined and a semi-supervised support vector machine (SVM) which separated stable participants from those who decline at follow-up with maximal margin. Cross-validated model performance metrics and MRI feature weights were calculated to include the strength of each brain voxel in its ability to distinguish the two groups. Results: Total model accuracy for predicting diagnostic change at follow-up was 92.7% using baseline T1 imaging alone, 83.5% using rsfMRI alone, and 94.5% when combining T1 and rsfMRI modalities. Feature weights that survived the p < 0.01 threshold for separation of the two groups revealed the strongest margin in the combined structural and functional regions underlying the medial temporal lobes in the limbic system. Discussion: An MRI-driven SVM model demonstrates accurate and precise prediction of later dementia conversion in aMCI patients. The multi-modal regions driving this prediction were the strongest in the medial temporal regions of the limbic system, consistent with literature on the progression of Alzheimer’s disease.