Publications by authors named "Jin Kyu Gahm"

Current deep learning methods for diagnosing Alzheimer's disease (AD) typically rely on analyzing all or parts of high-resolution 3D volumetric features, which demand expensive computational resources and powerful GPUs, particularly when using multimodal data. In contrast, lightweight cortical surface representations offer a more efficient approach for quantifying AD-related changes across different cortical regions, such as alterations in cortical structures, impaired glucose metabolism, and the deposition of pathological biomarkers like amyloid-β and tau. Despite these advantages, few studies have focused on diagnosing AD using multimodal surface-based data.

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Article Synopsis
  • Differences in iron accumulation patterns in atypical parkinsonian syndromes can be identified using susceptibility-weighted images, and deep learning methods are effective for this task.
  • Traditional deep learning models need large labeled datasets, which are expensive and can compromise patient privacy.
  • A new few-shot learning framework is proposed to distinguish between multiple system atrophy parkinsonian (MSA-P) and progressive supranuclear palsy (PSP) using fewer data samples, achieving better performance through enhanced feature identification and a novel hyperbolic space technique.
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Surface mapping is used in various brain imaging studies, such as for mapping gray matter atrophy patterns in Alzheimer's disease. Riemannian metrics on surface (RMOS) is a state-of-the-art surface mapping algorithm that optimizes Riemannian metrics to establish one-to-one correspondences between surfaces in the Laplace-Beltrami embedding space. However, owing to the complex calculation with accurate one-to-one correspondences, RMOS registration takes a long time.

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In recent studies, iron overload has been reported in atypical parkinsonian syndromes. The topographic patterns of iron distribution in deep brain nuclei vary by each subtype of parkinsonian syndrome, which is affected by underlying disease pathologies. In this study, we developed a novel framework that automatically analyzes the disease-specific patterns of iron accumulation using susceptibility weighted imaging (SWI).

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Optical Coherence Tomography Angiography (OCTA) is a novel, non-invasive imaging modality of retinal capillaries at micron resolution. Recent studies have correlated macular OCTA vascular measures with retinal disease severity and supported their use as a diagnostic tool. However, these measurements mostly rely on a few summary statistics in retinal layers or regions of interest in the two-dimensional (2D) en face projection images.

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Diabetic retinopathy (DR) is a significant microvascular complication of diabetes mellitus and a leading cause of vision impairment in working age adults. Optical coherence tomography (OCT) is a routinely used clinical tool to observe retinal structural and thickness alterations in DR. Pathological changes that alter the normal anatomy of the retina, such as intraretinal edema, pose great challenges for conventional layer-based analysis of OCT images.

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The significance of the transentorhinal (TE) cortex has been well known for the early diagnosis of Alzheimer's disease (AD). However, precise mapping of the TE cortex for the detection of local changes in the region was not well established mostly due to significant geometric variations around TE. In this paper, we propose a novel framework for automated patch generation of the TE cortex, patch-based mapping, and construction of an atlas with a distributed network.

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The superficial white matter (SWM) lies directly underneath the cortical ribbon and contains the short association fibers, or U-fibers, that connect neighboring gyri. Connectivity of these U-fibers is important for various neuroscientific research from the development to the aging of the brain. Nonetheless, conventional tractography methods can only provide a partial representation of these connections.

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Surface mapping methods play an important role in various brain imaging studies from tracking the maturation of adolescent brains to mapping gray matter atrophy patterns in Alzheimer's disease. Popular surface mapping approaches based on spherical registration, however, have inherent numerical limitations when severe metric distortions are present during the spherical parameterization step. In this paper, we propose a novel computational framework for intrinsic surface mapping in the Laplace-Beltrami (LB) embedding space based on Riemannian metric optimization on surfaces (RMOS).

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In brain shape analysis, the striatum is typically divided into three parts: the caudate, putamen, and accumbens nuclei for its analysis. Recent connectivity and animal studies, however, indicate striatum-cortical inter-connections do not always follow such subdivisions. For the holistic mapping of striatum surfaces, conventional spherical registration techniques are not suitable due to the large metric distortions in spherical parameterization of striatal surfaces.

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With the advance of human connectome research, there are great interests in computing diffeomorphic maps of brain surfaces with rich connectivity features. In this paper, we propose a novel framework for connectivity-driven surface mapping based on Riemannian metric optimization on surfaces (RMOS) in the Laplace-Beltrami (LB) embedding space. The mathematical foundation of our method is that we can use the pullback metric to define an isometry between surfaces for an arbitrary diffeomorphism, which in turn results in identical LB embeddings from the two surfaces.

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Correcting the effect of multiple testing is important in statistical parametric mapping. If the threshold is too liberal, then spurious claims may flood in; if it is too conservative, then true hints may be overlooked. It is highly desirable to combine random field theory and the false discovery rate (FDR) to achieve more powerful detection under gauged topological errors.

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Diffusion tensor magnetic resonance imaging (DT-MRI) is a technique used to quantify the microstructural organization of biological tissues. Multiple images are necessary to reconstruct the tensor data and each acquisition is subject to complex thermal noise. As such, measures of tensor invariants, which characterize components of tensor shape, derived from the tensor data will be biased from their true values.

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Purpose: Various methods exist for interpolating diffusion tensor fields, but none of them linearly interpolate tensor shape attributes. Linear interpolation is expected not to introduce spurious changes in tensor shape.

Methods: Herein we define a new linear invariant (LI) tensor interpolation method that linearly interpolates components of tensor shape (tensor invariants) and recapitulates the interpolated tensor from the linearly interpolated tensor invariants and the eigenvectors of a linearly interpolated tensor.

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