Like neocortical structures, the archicortical hippocampus differs in its folding patterns across individuals. Here, we present an automated and robust BIDS-App, HippUnfold, for defining and indexing individual-specific hippocampal folding in MRI, analogous to popular tools used in neocortical reconstruction. Such tailoring is critical for inter-individual alignment, with topology serving as the basis for homology. This topological framework enables qualitatively new analyses of morphological and laminar structure in the hippocampus or its subfields. It is critical for refining current neuroimaging analyses at a meso- as well as micro-scale. HippUnfold uses state-of-the-art deep learning combined with previously developed topological constraints to generate uniquely folded surfaces to fit a given subject's hippocampal conformation. It is designed to work with commonly employed sub-millimetric MRI acquisitions, with possible extension to microscopic resolution. In this paper we describe the power of HippUnfold in feature extraction, and highlight its unique value compared to several extant hippocampal subfield analysis methods.
The archicortical hippocampus differs, like the neocortex, in its folding patterns between individuals. Here, we present an automated and robust BIDS-App, HippUnfold, for defining and indexing subject-specific hippocampal folding in MRI, analogous to popular tools used in neocortical reconstruction. This is critical for inter-individual alignment, with topology as the basis for homology. This topological framework enables qualitatively new analyses of morphological and laminar structure in the hippocampus or hippocampal subfields, and is critical for the advancement of neuroimaging analyses at a meso- or micro-scale. HippUnfold uses state-of-the-art deep learning combined with previously developed topological constraints on hippocampal tissue. It is designed to work with commonly employed sub-millimetric MRI acquisitions, with extensibility to microscopic resolutions as well. In this paper we illustrate the power of HippUnfold in feature extraction, and its construct validity compared to several extant hippocampal subfield analysis methods.
Tools available for reproducible, quantitative assessment of brain correspondence have been limited. We previously validated the anatomical fiducial (AFID) placement protocol for point-based assessment of image registration with millimetric (mm) accuracy. In this data descriptor, we release curated AFID placements for some of the most commonly used structural magnetic resonance imaging datasets and templates. The release of our accurate placements allows for rapid quality control of image registration, teaching neuroanatomy, and clinical applications such as disease diagnosis and surgical targeting. We release placements on individual subjects from four datasets (N = 132 subjects for a total of 15,232 fiducials) and 14 brain templates (4,288 fiducials), totalling more than 300 human rater hours of annotation. We also validate human rater accuracy of released placements to be within 1 – 2 mm (using more than 45,000 Euclidean distances), consistent with prior studies. Our data is compliant with the Brain Imaging Data Structure allowing for facile incorporation into neuroimaging analysis pipelines.
The hippocampus is classically divided into mesoscopic subfields which contain varying microstructure that contribute to their unique functional roles. It has been challenging to characterize this microstructure with current MR based neuroimaging techniques. In this work, we used a novel surface-based approach in the hippocampus to show distinct microstructural distributions of myelin, neurite density and dispersion, fractional anisotropy, and mean diffusivity using diffusion MRI. To get at this issue we used the Neurite Orientation Dispersion and Density Imaging (NODDI) model optimized for gray matter diffusivity and diffusion tensor imaging (DTI). We found that neurite dispersion was highest in the Cornu Ammonis (CA) 1 and subiculum subfields which likely captures the large heterogeneity of tangential and radial fibers, such as the Schaffer collaterals, perforant path, and pyramidal neurites. Neurite density and myelin content were highest in the subiculum and lowest in CA1, which may reflect known myeloarchitecture differences between these subfields. We show macrostructural measures of gyrification, thickness, and curvature which were in line with ex vivo descriptions of hippocampal anatomy. We employed a multivariate orthogonal projective non-negative matrix factorization (OPNNMF) approach to capture co-varying regions of macro- and microstructure across the hippocampus. The clusters were highly variable along the medial-lateral (proximal-distal) direction, which is expected as there are known differences in morphology, cytoarchitectonic profiles, and connectivity. Long-axis (anterior-posterior) differences can also be seen in the OPNNMF components, where the body of the hippocampus has more parcellations than the head and tail. Finally, we show that by examining the main direction of diffusion relative to canonical hippocampal axes, we could identify microstructure that may map onto specific tangential fiber pathways, such as the Schaffer collaterals and perforant path. These results highlight the value of combining in vivo diffusion MRI with computational approaches for capturing hippocampal microstructure, which may provide useful features for understanding cognition and for diagnosis of disease states.
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