arXiv subjects

Vince D. Calhoun

Publications and source records attributed to Vince D. Calhoun.

At least 55 records · Page 3Linked to original sources

arXiv2024

Multimodal MRI Accurately Identifies Amyloid Status in Unbalanced Cohorts in Alzheimer's Disease Continuum

Amyloid-$β$ (A$β$) plaques in conjunction with hyperphosphorylated tau proteins in the form of neurofibrillary tangles are the two neuropathological hallmarks of Alzheimer's disease. It is well-known that the identification of individuals with A$β$ positivity could enable early diagnosis. In this work, we aim at capturing the A$β$ positivity status in an unbalanced cohort enclosing subjects at different disease stages, exploiting the underlying structural and connectivity disease-induced modulations as revealed by structural, functional, and diffusion MRI. Of note, due to the unbalanced cohort, the outcomes may be guided by those factors rather than amyloid accumulation. The partial views provided by each modality are integrated in the model allowing to take full advantage of their complementarity in encoding the effects of the A$β$ accumulation, leading to an accuracy of $0.762\pm0.04$. The specificity of the information brought by each modality is assessed by \textit{post-hoc} explainability analysis (guided backpropagation), highlighting the underlying structural and functional changes. Noteworthy, well-established biomarker key regions related to A$β$ deposition could be identified by all modalities, including the hippocampus, thalamus, precuneus, and cingulate gyrus, witnessing in favor of the reliability of the method as well as its potential in shading light on modality-specific possibly unknown A$β$ deposition signatures.

cs.AI↗

arXiv2024

A deep spatio-temporal attention model of dynamic functional network connectivity shows sensitivity to Alzheimer's in asymptomatic individuals

Alzheimer's disease (AD) progresses from asymptomatic changes to clinical symptoms, emphasizing the importance of early detection for proper treatment. Functional magnetic resonance imaging (fMRI), particularly dynamic functional network connectivity (dFNC), has emerged as an important biomarker for AD. Nevertheless, studies probing at-risk subjects in the pre-symptomatic stage using dFNC are limited. To identify at-risk subjects and understand alterations of dFNC in different stages, we leverage deep learning advancements and introduce a transformer-convolution framework for predicting at-risk subjects based on dFNC, incorporating spatial-temporal self-attention to capture brain network dependencies and temporal dynamics. Our model significantly outperforms other popular machine learning methods. By analyzing individuals with diagnosed AD and mild cognitive impairment (MCI), we studied the AD progression and observed a higher similarity between MCI and asymptomatic AD. The interpretable analysis highlights the cognitive-control network's diagnostic importance, with the model focusing on intra-visual domain dFNC when predicting asymptomatic AD subjects.

cs.CE↗

arXiv2024

Multi-modal Imaging Genomics Transformer: Attentive Integration of Imaging with Genomic Biomarkers for Schizophrenia Classification

Schizophrenia (SZ) is a severe brain disorder marked by diverse cognitive impairments, abnormalities in brain structure, function, and genetic factors. Its complex symptoms and overlap with other psychiatric conditions challenge traditional diagnostic methods, necessitating advanced systems to improve precision. Existing research studies have mostly focused on imaging data, such as structural and functional MRI, for SZ diagnosis. There has been less focus on the integration of genomic features despite their potential in identifying heritable SZ traits. In this study, we introduce a Multi-modal Imaging Genomics Transformer (MIGTrans), that attentively integrates genomics with structural and functional imaging data to capture SZ-related neuroanatomical and connectome abnormalities. MIGTrans demonstrated improved SZ classification performance with an accuracy of 86.05% (+/- 0.02), offering clear interpretations and identifying significant genomic locations and brain morphological/connectivity patterns associated with SZ.

cs.CV↗

arXiv2024

Spectral Introspection Identifies Group Training Dynamics in Deep Neural Networks for Neuroimaging

Neural networks, whice have had a profound effect on how researchers study complex phenomena, do so through a complex, nonlinear mathematical structure which can be difficult for human researchers to interpret. This obstacle can be especially salient when researchers want to better understand the emergence of particular model behaviors such as bias, overfitting, overparametrization, and more. In Neuroimaging, the understanding of how such phenomena emerge is fundamental to preventing and informing users of the potential risks involved in practice. In this work, we present a novel introspection framework for Deep Learning on Neuroimaging data, which exploits the natural structure of gradient computations via the singular value decomposition of gradient components during reverse-mode auto-differentiation. Unlike post-hoc introspection techniques, which require fully-trained models for evaluation, our method allows for the study of training dynamics on the fly, and even more interestingly, allow for the decomposition of gradients based on which samples belong to particular groups of interest. We demonstrate how the gradient spectra for several common deep learning models differ between schizophrenia and control participants from the COBRE study, and illustrate how these trajectories may reveal specific training dynamics helpful for further analysis.

cs.LG↗

arXiv2024

A Demographic-Conditioned Variational Autoencoder for fMRI Distribution Sampling and Removal of Confounds

Objective: fMRI and derived measures such as functional connectivity (FC) have been used to predict brain age, general fluid intelligence, psychiatric disease status, and preclinical neurodegenerative disease. However, it is not always clear that all demographic confounds, such as age, sex, and race, have been removed from fMRI data. Additionally, many fMRI datasets are restricted to authorized researchers, making dissemination of these valuable data sources challenging. Methods: We create a variational autoencoder (VAE)-based model, DemoVAE, to decorrelate fMRI features from demographics and generate high-quality synthetic fMRI data based on user-supplied demographics. We train and validate our model using two large, widely used datasets, the Philadelphia Neurodevelopmental Cohort (PNC) and Bipolar and Schizophrenia Network for Intermediate Phenotypes (BSNIP). Results: We find that DemoVAE recapitulates group differences in fMRI data while capturing the full breadth of individual variations. Significantly, we also find that most clinical and computerized battery fields that are correlated with fMRI data are not correlated with DemoVAE latents. An exception are several fields related to schizophrenia medication and symptom severity. Conclusion: Our model generates fMRI data that captures the full distribution of FC better than traditional VAE or GAN models. We also find that most prediction using fMRI data is dependent on correlation with, and prediction of, demographics. Significance: Our DemoVAE model allows for generation of high quality synthetic data conditioned on subject demographics as well as the removal of the confounding effects of demographics. We identify that FC-based prediction tasks are highly influenced by demographic confounds.

q-bio.QM↗

arXiv2024

Cross-Modality Translation with Generative Adversarial Networks to Unveil Alzheimer's Disease Biomarkers

Generative approaches for cross-modality transformation have recently gained significant attention in neuroimaging. While most previous work has focused on case-control data, the application of generative models to disorder-specific datasets and their ability to preserve diagnostic patterns remain relatively unexplored. Hence, in this study, we investigated the use of a generative adversarial network (GAN) in the context of Alzheimer's disease (AD) to generate functional network connectivity (FNC) and T1-weighted structural magnetic resonance imaging data from each other. We employed a cycle-GAN to synthesize data in an unpaired data transition and enhanced the transition by integrating weak supervision in cases where paired data were available. Our findings revealed that our model could offer remarkable capability, achieving a structural similarity index measure (SSIM) of $0.89 \pm 0.003$ for T1s and a correlation of $0.71 \pm 0.004$ for FNCs. Moreover, our qualitative analysis revealed similar patterns between generated and actual data when comparing AD to cognitively normal (CN) individuals. In particular, we observed significantly increased functional connectivity in cerebellar-sensory motor and cerebellar-visual networks and reduced connectivity in cerebellar-subcortical, auditory-sensory motor, sensory motor-visual, and cerebellar-cognitive control networks. Additionally, the T1 images generated by our model showed a similar pattern of atrophy in the hippocampal and other temporal regions of Alzheimer's patients.

q-bio.NC↗

arXiv2024

Persistent Homological State-Space Estimation of Functional Human Brain Networks at Rest

We introduce an innovative, data-driven topological data analysis (TDA) technique for estimating the state spaces of dynamically changing functional human brain networks at rest. Our method utilizes the Wasserstein distance to measure topological differences, enabling the clustering of brain networks into distinct topological states. This technique outperforms the commonly used k-means clustering in identifying brain network state spaces by effectively incorporating the temporal dynamics of the data without the need for explicit model specification. We further investigate the genetic underpinnings of these topological features using a twin study design, examining the heritability of such state changes. Our findings suggest that the topology of brain networks, particularly in their dynamic state changes, may hold significant hidden genetic information. MATLAB code for the method is available at https://github.com/laplcebeltrami/PH-STAT.

math.AT↗

arXiv2024

Multiscale Neuroimaging Features for the Identification of Medication Class and Non-Responders in Mood Disorder Treatment

In the clinical treatment of mood disorders, the complex behavioral symptoms presented by patients and variability of patient response to particular medication classes can create difficulties in providing fast and reliable treatment when standard diagnostic and prescription methods are used. Increasingly, the incorporation of physiological information such as neuroimaging scans and derivatives into the clinical process promises to alleviate some of the uncertainty surrounding this process. Particularly, if neural features can help to identify patients who may not respond to standard courses of anti-depressants or mood stabilizers, clinicians may elect to avoid lengthy and side-effect-laden treatments and seek out a different, more effective course that might otherwise not have been under consideration. Previously, approaches for the derivation of relevant neuroimaging features work at only one scale in the data, potentially limiting the depth of information available for clinical decision support. In this work, we show that the utilization of multi spatial scale neuroimaging features - particularly resting state functional networks and functional network connectivity measures - provide a rich and robust basis for the identification of relevant medication class and non-responders in the treatment of mood disorders. We demonstrate that the generated features, along with a novel approach for fast and automated feature selection, can support high accuracy rates in the identification of medication class and non-responders as well as the identification of novel, multi-scale biomarkers.

cs.LG↗

arXiv2024

Low-Rank Learning by Design: the Role of Network Architecture and Activation Linearity in Gradient Rank Collapse

Our understanding of learning dynamics of deep neural networks (DNNs) remains incomplete. Recent research has begun to uncover the mathematical principles underlying these networks, including the phenomenon of "Neural Collapse", where linear classifiers within DNNs converge to specific geometrical structures during late-stage training. However, the role of geometric constraints in learning extends beyond this terminal phase. For instance, gradients in fully-connected layers naturally develop a low-rank structure due to the accumulation of rank-one outer products over a training batch. Despite the attention given to methods that exploit this structure for memory saving or regularization, the emergence of low-rank learning as an inherent aspect of certain DNN architectures has been under-explored. In this paper, we conduct a comprehensive study of gradient rank in DNNs, examining how architectural choices and structure of the data effect gradient rank bounds. Our theoretical analysis provides these bounds for training fully-connected, recurrent, and convolutional neural networks. We also demonstrate, both theoretically and empirically, how design choices like activation function linearity, bottleneck layer introduction, convolutional stride, and sequence truncation influence these bounds. Our findings not only contribute to the understanding of learning dynamics in DNNs, but also provide practical guidance for deep learning engineers to make informed design decisions.

cs.LG↗

arXiv2024

The Past, Present, and Future of the Brain Imaging Data Structure (BIDS)

The Brain Imaging Data Structure (BIDS) is a community-driven standard for the organization of data and metadata from a growing range of neuroscience modalities. This paper is meant as a history of how the standard has developed and grown over time. We outline the principles behind the project, the mechanisms by which it has been extended, and some of the challenges being addressed as it evolves. We also discuss the lessons learned through the project, with the aim of enabling researchers in other domains to learn from the success of BIDS.

q-bio.OT↗

arXiv2023

Improving age prediction: Utilizing LSTM-based dynamic forecasting for data augmentation in multivariate time series analysis

The high dimensionality and complexity of neuroimaging data necessitate large datasets to develop robust and high-performing deep learning models. However, the neuroimaging field is notably hampered by the scarcity of such datasets. In this work, we proposed a data augmentation and validation framework that utilizes dynamic forecasting with Long Short-Term Memory (LSTM) networks to enrich datasets. We extended multivariate time series data by predicting the time courses of independent component networks (ICNs) in both one-step and recursive configurations. The effectiveness of these augmented datasets was then compared with the original data using various deep learning models designed for chronological age prediction tasks. The results suggest that our approach improves model performance, providing a robust solution to overcome the challenges presented by the limited size of neuroimaging datasets.

cs.LG↗

arXiv2023

Constrained Independent Vector Analysis with Reference for Multi-Subject fMRI Analysis

Independent component analysis (ICA) is now a widely used solution for the analysis of multi-subject functional magnetic resonance imaging (fMRI) data. Independent vector analysis (IVA) generalizes ICA to multiple datasets, i.e., to multi-subject data, and in addition to higher-order statistical information in ICA, it leverages the statistical dependence across the datasets as an additional type of statistical diversity. As such, it preserves variability in the estimation of single-subject maps but its performance might suffer when the number of datasets increases. Constrained IVA is an effective way to bypass computational issues and improve the quality of separation by incorporating available prior information. Existing constrained IVA approaches often rely on user-defined threshold values to define the constraints. However, an improperly selected threshold can have a negative impact on the final results. This paper proposes two novel methods for constrained IVA: one using an adaptive-reverse scheme to select variable thresholds for the constraints and a second one based on a threshold-free formulation by leveraging the unique structure of IVA. We demonstrate that our solutions provide an attractive solution to multi-subject fMRI analysis both by simulations and through analysis of resting state fMRI data collected from 98 subjects -- the highest number of subjects ever used by IVA algorithms. Our results show that both proposed approaches obtain significantly better separation quality and model match while providing computationally efficient and highly reproducible solutions.

eess.SP↗

arXiv2023

Aberrant High-Order Dependencies in Schizophrenia Resting-State Functional MRI Networks

The human brain has a complex, intricate functional architecture. While many studies primarily emphasize pairwise interactions, delving into high-order associations is crucial for a comprehensive understanding of how functional brain networks intricately interact beyond simple pairwise connections. Analyzing high-order statistics allows us to explore the nuanced and complex relationships across the brain, unraveling the heterogeneity and uncovering patterns of multilevel overlap on the psychosis continuum. Here, we employed high-order independent component analysis (ICA) plus multivariate information-theoretical metrics ($O$-information and $S$-information) to estimate high-order interaction to examine schizophrenia using resting-state fMRI. The results show that multiple brain regions networks may be altered in schizophrenia, such as temporal, subcortical, and higher-cognitive brain regions, and meanwhile, it also shows that revealed synergy gives more information than redundancy in diagnosing schizophrenia. All in all, we showed that high-order dependencies were altered in schizophrenia. Identification of these aberrant patterns will give us a new window to diagnose schizophrenia.

q-bio.NC↗

arXiv2023

Predictive Sparse Manifold Transform

We present Predictive Sparse Manifold Transform (PSMT), a minimalistic, interpretable and biologically plausible framework for learning and predicting natural dynamics. PSMT incorporates two layers where the first sparse coding layer represents the input sequence as sparse coefficients over an overcomplete dictionary and the second manifold learning layer learns a geometric embedding space that captures topological similarity and dynamic temporal linearity in sparse coefficients. We apply PSMT on a natural video dataset and evaluate the reconstruction performance with respect to contextual variability, the number of sparse coding basis functions and training samples. We then interpret the dynamic topological organization in the embedding space. We next utilize PSMT to predict future frames compared with two baseline methods with a static embedding space. We demonstrate that PSMT with a dynamic embedding space can achieve better prediction performance compared to static baselines. Our work establishes that PSMT is an efficient unsupervised generative framework for prediction of future visual stimuli.

stat.ML↗

arXiv2023

Looking deeper into interpretable deep learning in neuroimaging: a comprehensive survey

Deep learning (DL) models have been popular due to their ability to learn directly from the raw data in an end-to-end paradigm, alleviating the concern of a separate error-prone feature extraction phase. Recent DL-based neuroimaging studies have also witnessed a noticeable performance advancement over traditional machine learning algorithms. But the challenges of deep learning models still exist because of the lack of transparency in these models for their successful deployment in real-world applications. In recent years, Explainable AI (XAI) has undergone a surge of developments mainly to get intuitions of how the models reached the decisions, which is essential for safety-critical domains such as healthcare, finance, and law enforcement agencies. While the interpretability domain is advancing noticeably, researchers are still unclear about what aspect of model learning a post hoc method reveals and how to validate its reliability. This paper comprehensively reviews interpretable deep learning models in the neuroimaging domain. Firstly, we summarize the current status of interpretability resources in general, focusing on the progression of methods, associated challenges, and opinions. Secondly, we discuss how multiple recent neuroimaging studies leveraged model interpretability to capture anatomical and functional brain alterations most relevant to model predictions. Finally, we discuss the limitations of the current practices and offer some valuable insights and guidance on how we can steer our future research directions to make deep learning models substantially interpretable and thus advance scientific understanding of brain disorders.

cs.LG↗

arXiv2022

Latent Similarity Identifies Important Functional Connections for Phenotype Prediction

Objective: Endophenotypes such as brain age and fluid intelligence are important biomarkers of disease status. However, brain imaging studies to identify these biomarkers often encounter limited numbers of subjects and high dimensional imaging features, hindering reproducibility. Therefore, we develop an interpretable, multivariate classification/regression algorithm, called Latent Similarity (LatSim), suitable for small sample size, high feature dimension datasets. Methods: LatSim combines metric learning with a kernel similarity function and softmax aggregation to identify task-related similarities between subjects. Inter-subject similarity is utilized to improve performance on three prediction tasks using multi-paradigm fMRI data. A greedy selection algorithm, made possible by LatSim's computational efficiency, is developed as an interpretability method. Results: LatSim achieved significantly higher predictive accuracy at small sample sizes on the Philadelphia Neurodevelopmental Cohort (PNC) dataset. Connections identified by LatSim gave superior discriminative power compared to those identified by other methods. We identified 4 functional brain networks enriched in connections for predicting brain age, sex, and intelligence. Conclusion: We find that most information for a predictive task comes from only a few (1-5) connections. Additionally, we find that the default mode network is over-represented in the top connections of all predictive tasks. Significance: We propose a novel algorithm for small sample, high feature dimension datasets and use it to identify connections in task fMRI data. Our work should lead to new insights in both algorithm design and neuroscience research. Code and demo are available at https://github.com/aorliche/LatentSimilarity/.

q-bio.QM↗

arXiv2022

New Interpretable Patterns and Discriminative Features from Brain Functional Network Connectivity Using Dictionary Learning

Independent component analysis (ICA) of multi-subject functional magnetic resonance imaging (fMRI) data has proven useful in providing a fully multivariate summary that can be used for multiple purposes. ICA can identify patterns that can discriminate between healthy controls (HC) and patients with various mental disorders such as schizophrenia (Sz). Temporal functional network connectivity (tFNC) obtained from ICA can effectively explain the interactions between brain networks. On the other hand, dictionary learning (DL) enables the discovery of hidden information in data using learnable basis signals through the use of sparsity. In this paper, we present a new method that leverages ICA and DL for the identification of directly interpretable patterns to discriminate between the HC and Sz groups. We use multi-subject resting-state fMRI data from $358$ subjects and form subject-specific tFNC feature vectors from ICA results. Then, we learn sparse representations of the tFNCs and introduce a new set of sparse features as well as new interpretable patterns from the learned atoms. Our experimental results show that the new representation not only leads to effective classification between HC and Sz groups using sparse features, but can also identify new interpretable patterns from the learned atoms that can help understand the complexities of mental diseases such as schizophrenia.

q-bio.NC↗

arXiv2022

Self-supervised multimodal neuroimaging yields predictive representations for a spectrum of Alzheimer's phenotypes

Recent neuroimaging studies that focus on predicting brain disorders via modern machine learning approaches commonly include a single modality and rely on supervised over-parameterized models.However, a single modality provides only a limited view of the highly complex brain. Critically, supervised models in clinical settings lack accurate diagnostic labels for training. Coarse labels do not capture the long-tailed spectrum of brain disorder phenotypes, which leads to a loss of generalizability of the model that makes them less useful in diagnostic settings. This work presents a novel multi-scale coordinated framework for learning multiple representations from multimodal neuroimaging data. We propose a general taxonomy of informative inductive biases to capture unique and joint information in multimodal self-supervised fusion. The taxonomy forms a family of decoder-free models with reduced computational complexity and a propensity to capture multi-scale relationships between local and global representations of the multimodal inputs. We conduct a comprehensive evaluation of the taxonomy using functional and structural magnetic resonance imaging (MRI) data across a spectrum of Alzheimer's disease phenotypes and show that self-supervised models reveal disorder-relevant brain regions and multimodal links without access to the labels during pre-training. The proposed multimodal self-supervised learning yields representations with improved classification performance for both modalities. The concomitant rich and flexible unsupervised deep learning framework captures complex multimodal relationships and provides predictive performance that meets or exceeds that of a more narrow supervised classification analysis. We present elaborate quantitative evidence of how this framework can significantly advance our search for missing links in complex brain disorders.

cs.LG↗