SearcharxivSearch

arXiv subjects

Peter Kochunov

Publications and source records attributed to Peter Kochunov.

10 recordsLinked to original sources

Normative Cerebral Perfusion Across the Lifespan

Cerebral perfusion plays a crucial role in maintaining brain function and is tightly coupled with neuronal activity. While previous studies have examined cerebral perfusion trajectories across development and aging, precise characterization of its lifespan dynamics has been limited by small sample sizes and methodological inconsistencies. In this study, we construct the first comprehensive normative model of cerebral perfusion across the human lifespan (birth to 85 years) using a large multi-site dataset of over 12,000 high-quality arterial spin labeling (ASL) MRI scans. Leveraging generalized additive models for location, scale, and shape (GAMLSS), we mapped nonlinear growth trajectories of cerebral perfusion at global, network, and regional levels. We observed a rapid postnatal increase in cerebral perfusion, peaking at approximately 7.1 years, followed by a gradual decline into adulthood. Sex differences were evident, with distinct regional maturation patterns rather than uniform differences across all brain regions. Beyond normative modeling, we quantified individual deviations from expected CBF patterns in neurodegenerative and psychiatric conditions, identifying disease-specific perfusion abnormalities across four brain disorders. Using longitudinal data, we established typical and atypical cerebral perfusion trajectories, highlighting the prognostic value of perfusion-based biomarkers for detecting disease progression. Our findings provide a robust normative framework for cerebral perfusion, facilitating precise characterization of brain health across the lifespan and enhancing the early identification of neurovascular dysfunction in clinical populations.

q-bio.NC

Integrative data analysis where partial covariates have complex non-linear effects by using summary information from an external data

A full parametric and linear specification may be insufficient to capture complicated patterns in studies exploring complex features, such as those investigating age-related changes in brain functional abilities. Alternatively, a partially linear model (PLM) consisting of both parametric and non-parametric elements may have a better fit. This model has been widely applied in economics, environmental science, and biomedical studies. In this paper, we introduce a novel statistical inference framework that equips PLM with high estimation efficiency by effectively synthesizing summary information from external data into the main analysis. Such an integrative scheme is versatile in assimilating various types of reduced models from the external study. The proposed method is shown to be theoretically valid and numerically convenient, and it ensures a high-efficiency gain compared to classic methods in PLM. Our method is further validated using two data applications by evaluating the risk factors of brain imaging measures and blood pressure.

stat.ME

Multiple Imputation Method for High-Dimensional Neuroimaging Data

Missingness is a common issue for neuroimaging data, and neglecting it in downstream statistical analysis can introduce bias and lead to misguided inferential conclusions. It is therefore crucial to conduct appropriate statistical methods to address this issue. While multiple imputation is a popular technique for handling missing data, its application to neuroimaging data is hindered by high dimensionality and complex dependence structures of multivariate neuroimaging variables. To tackle this challenge, we propose a novel approach, named High Dimensional Multiple Imputation (HIMA), based on Bayesian models. HIMA develops a new computational strategy for sampling large covariance matrices based on a robustly estimated posterior mode, which drastically enhances computational efficiency and numerical stability. To assess the effectiveness of HIMA, we conducted extensive simulation studies and real-data analysis using neuroimaging data from a Schizophrenia study. HIMA showcases a computational efficiency improvement of over 2000 times when compared to traditional approaches, while also producing imputed datasets with improved precision and stability.

stat.ME

Evaluating the effects of high-throughput structural neuroimaging predictors on whole-brain functional connectome outcomes via network-based vector-on-matrix regression

The joint analysis of multimodal neuroimaging data is critical in the field of brain research because it reveals complex interactive relationships between neurobiological structures and functions. In this study, we focus on investigating the effects of structural imaging (SI) features, including white matter micro-structure integrity (WMMI) and cortical thickness, on the whole brain functional connectome (FC) network. To achieve this goal, we propose a network-based vector-on-matrix regression model to characterize the FC-SI association patterns. We have developed a novel multi-level dense bipartite and clique subgraph extraction method to identify which subsets of spatially specific SI features intensively influence organized FC sub-networks. The proposed method can simultaneously identify highly correlated structural-connectomic association patterns and suppress false positive findings while handling millions of potential interactions. We apply our method to a multimodal neuroimaging dataset of 4,242 participants from the UK Biobank to evaluate the effects of whole-brain WMMI and cortical thickness on the resting-state FC. The results reveal that the WMMI on corticospinal tracts and inferior cerebellar peduncle significantly affect functional connections of sensorimotor, salience, and executive sub-networks with an average correlation of 0.81 (p<0.001).

stat.ME

Network method for voxel-pair-level brain connectivity analysis under spatial-contiguity constraints

Brain connectome analysis commonly compresses high-resolution brain scans (typically composed of millions of voxels) down to only hundreds of regions of interest (ROIs) by averaging within-ROI signals. This huge dimension reduction improves computational speed and the morphological properties of anatomical structures; however, it also comes at the cost of substantial losses in spatial specificity and sensitivity, especially when the signals exhibit high within-ROI heterogeneity. Oftentimes, abnormally expressed functional connectivity (FC) between a pair of ROIs caused by a brain disease is primarily driven by only small subsets of voxel pairs within the ROI pair. This article proposes a new network method for detection of voxel-pair-level neural dysconnectivity with spatial constraints. Specifically, focusing on an ROI pair, our model aims to extract dense sub-areas that contain aberrant voxel-pair connections while ensuring that the involved voxels are spatially contiguous. In addition, we develop sub-community-detection algorithms to realize the model, and the consistency of these algorithms is justified. Comprehensive simulation studies demonstrate our method's effectiveness in reducing the false-positive rate while increasing statistical power, detection replicability, and spatial specificity. We apply our approach to reveal: (i) voxel-wise schizophrenia-altered FC patterns within the salience and temporal-thalamic network from 330 participants in a schizophrenia study; (ii) disrupted voxel-wise FC patterns related to nicotine addiction between the basal ganglia, hippocampus, and insular gyrus from 3269 participants using UK Biobank data. The detected results align with previous medical findings but include improved localized information.

stat.ME

Deep Learning for Quality Control of Subcortical Brain 3D Shape Models

We present several deep learning models for assessing the morphometric fidelity of deep grey matter region models extracted from brain MRI. We test three different convolutional neural net architectures (VGGNet, ResNet and Inception) over 2D maps of geometric features. Further, we present a novel geometry feature augmentation technique based on a parametric spherical mapping. Finally, we present an approach for model decision visualization, allowing human raters to see the areas of subcortical shapes most likely to be deemed of failing quality by the machine. Our training data is comprised of 5200 subjects from the ENIGMA Schizophrenia MRI cohorts, and our test dataset contains 1500 subjects from the ENIGMA Major Depressive Disorder cohorts. Our final models reduce human rater time by 46-70%. ResNet outperforms VGGNet and Inception for all of our predictive tasks.

q-bio.NC

Overlaying Quantitative Measurement on Networks: An Evaluation of Three Positioning and Nine Visual Marker Techniques

We report results from an experiment on ranking visual markers and node positioning techniques for network visualizations. Inspired by prior ranking studies, we rethink the ranking when the dataset size increases and when the markers are distributed in space. Centrality indices are visualized as node attributes. Our experiment studies nine visual markers and three positioning methods. Our results suggest that direct encoding of quantities improves accuracy by about 20% compared to previous results. Of the three positioning techniques, circular was always in the top group, and matrix and projection switch orders depending on two factors: whether or not the tasks demand symmetry, or the nodes are within closely proximity. Among the most interesting results of ranking the visual markers for comparison tasks are that hue and area fall into the top groups for nearly all multi-scale comparison tasks; Shape (ordered by curvature) is perhaps not as scalable as we have thought and can support more accurate answers only when two quantities are compared; Lightness and slope are least accurate for quantitative comparisons regardless of scale of the comparison tasks. Our experiment is among the first to acquire a complete picture of ranking visual markers in different scales for comparison tasks.

cs.GR

Heritability estimates on resting state fMRI data using the ENIGMA analysis pipeline

Big data initiatives such as the Enhancing NeuroImaging Genetics through Meta-Analysis consortium (ENIGMA), combine data collected by independent studies worldwide to achieve more accurate estimates of effect sizes and more reliable and reproducible outcomes. Such efforts require harmonized analyses protocols to consistently extract phenotypes. Even so, challenges include wide variability of fMRI protocols and scanner platforms; this leads to site-to-site variance in quality, resolution and temporal signal-to-noise ratio (tSNR). An effective harmonization should provide optimal measures for data of different qualities. We developed a multi-site rsfMRI analysis pipeline to allow research groups around the world to process rsfMRI scans in a harmonized way, to extract consistent and quantitative measurements of connectivity and to perform coordinated statistical tests. We used the single-modality ENIGMA rsfMRI pipeline based on model-free Marchenko-Pastor PCA based denoising to verify and replicate findings of significant heritability of measures from resting state networks. We analyzed two independent cohorts, GOBS (Genetics of Brain Structure) and HCP (the Human Connectome Project), which collected data using conventional and connectomics oriented fMRI protocols. We used seed-based connectivity and dual-regression approaches to show that rsfMRI signal is consistently heritable across twenty major functional network measures. Heritability values of 20-40% were observed across both cohorts.

q-bio.NC

Machine Learning for Large-Scale Quality Control of 3D Shape Models in Neuroimaging

As very large studies of complex neuroimaging phenotypes become more common, human quality assessment of MRI-derived data remains one of the last major bottlenecks. Few attempts have so far been made to address this issue with machine learning. In this work, we optimize predictive models of quality for meshes representing deep brain structure shapes. We use standard vertex-wise and global shape features computed homologously across 19 cohorts and over 7500 human-rated subjects, training kernelized Support Vector Machine and Gradient Boosted Decision Trees classifiers to detect meshes of failing quality. Our models generalize across datasets and diseases, reducing human workload by 30-70\%, or equivalently hundreds of human rater hours for datasets of comparable size, with recall rates approaching inter-rater reliability.

q-bio.QM

A Network Object Method to Uncover Hidden Disorder-Related Brain Connectome

Neuropsychiatric disorders impact functional connectivity of the brain at the network level. The identification and statistical testing of disorder-related networks remains challenging. We propose novel methods to streamline the detection and testing of the hidden, disorder-related connectivity patterns as network-objects. We define an abnormal connectome subnetwork as a network-object that includes three classes: nodes of brain areas, edges representing brain connectomic features, and an organized graph topology formed by these nodes and edges. Comparing to the conventional statistical methods, the proposed approach simultaneously reduces false positive and negative discovery rates by letting edges borrow strengths precisely with the guidance of graph topological information, which effectively improves the reproducibility of findings across brain connectome studies. The network-object analyses may provide insights into how brain connectome is systematically impaired by brain illnesses.

stat.AP