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Jun Young Park

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3 papers

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YNIMG Journal 2022 Journal Article

CLEAN: Leveraging spatial autocorrelation in neuroimaging data in clusterwise inference

Jun Young Park
Mark Fiecas

While clusterwise inference is a popular approach in neuroimaging that improves sensitivity, current methods do not account for explicit spatial autocorrelations because most use univariate test statistics to construct cluster-extent statistics. Failure to account for such dependencies could result in decreased reproducibility. To address methodological and computational challenges, we propose a new powerful and fast statistical method called CLEAN (Clusterwise inference Leveraging spatial Autocorrelations in Neuroimaging). CLEAN computes multivariate test statistics by modelling brain-wise spatial autocorrelations, constructs cluster-extent test statistics, and applies a refitting-free resampling approach to control false positives. We validate CLEAN using simulations and applications to the Human Connectome Project. This novel method provides a new direction in neuroimaging that paces with advances in high-resolution MRI data which contains a substantial amount of spatial autocorrelation.

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YNIMG Journal 2022 Journal Article

Spatially-enhanced clusterwise inference for testing and localizing intermodal correspondence

Sarah M. Weinstein
Simon N. Vandekar
Erica B. Baller
Danni Tu
Azeez Adebimpe
Tinashe M. Tapera
Ruben C. Gur
Raquel E. Gur

With the increasing availability of neuroimaging data from multiple modalities-each providing a different lens through which to study brain structure or function-new techniques for comparing, integrating, and interpreting information within and across modalities have emerged. Recent developments include hypothesis tests of associations between neuroimaging modalities, which can be used to determine the statistical significance of intermodal associations either throughout the entire brain or within anatomical subregions or functional networks. While these methods provide a crucial foundation for inference on intermodal relationships, they cannot be used to answer questions about where in the brain these associations are most pronounced. In this paper, we introduce a new method, called CLEAN-R, that can be used both to test intermodal correspondence throughout the brain and also to localize this correspondence. Our method involves first adjusting for the underlying spatial autocorrelation structure within each modality before aggregating information within small clusters to construct a map of enhanced test statistics. Using structural and functional magnetic resonance imaging data from a subsample of children and adolescents from the Philadelphia Neurodevelopmental Cohort, we conduct simulations and data analyses where we illustrate the high statistical power and nominal type I error levels of our method. By constructing an interpretable map of group-level correspondence using spatially-enhanced test statistics, our method offers insights beyond those provided by earlier methods.

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YNIMG Journal 2021 Journal Article

Permutation-based inference for spatially localized signals in longitudinal MRI data

Jun Young Park
Mark Fiecas

Alzheimer's disease is a neurodegenerative disease in which the degree of cortical atrophy in specific structures of the brain serves as a useful imaging biomarker. Recent approaches using linear mixed effects (LME) models in longitudinal neuroimaging have been powerful and flexible in investigating the temporal trajectories of cortical thickness. However, massive-univariate analysis, a simplified approach that obtains a summary statistic (e.g., a p-value) for every vertex along the cortex, is insufficient to model cortical atrophy because it does not account for spatial similarities of the signals in neighboring locations. In this article, we develop a permutation-based inference procedure to detect spatial clusters of vertices showing statistically significant differences in the rates of cortical atrophy. The proposed method, called SpLoc, uses spatial information to combine the signals adaptively across neighboring vertices, yielding high statistical power while controlling family-wise error rate (FWER) accurately. When we reject the global null hypothesis, we use a cluster selection algorithm to detect the spatial clusters of significant vertices. We validate our method using simulation studies and apply it to the Alzheimer's Disease Neuroimaging Initiative (ADNI) data to show its superior performance over existing methods. An R package for implementing SpLoc is publicly available.

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