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Mueller-Axt, C.

Publications and source records attributed to Mueller-Axt, C..

2 recordsLinked to original sources

A critical assessment of LGN segmentation quality based on volume, contour, and location

Reliable segmentation of the lateral geniculate nucleus (LGN), a small thalamic relay nucleus essential for visual processing, is necessary for characterizing its anatomy in healthy populations and structural alterations in neurological disorders. However, accurate delineation remains challenging on routinely acquired T1-weighted images because the LGN is small, deeply located, and has limited contrast relative to surrounding thalamic tissue. Although manual segmentation remains the reference standard, it is time consuming and susceptible to rater variability, limiting its use in large datasets. Automated approaches may therefore provide a more scalable alternative. In this study, we performed a systematic benchmarking of seven automated approaches: FreeSurfer, NextBrain, DeepThalamus, HIPS-THOMAS, MASSP 2.0, BigBrain alignment, and manual novice segmentation against expert-defined ground truth. We applied a multi-metric evaluation incorporating the Dice similarity coefficient, Hausdorff distance and balanced average Hausdorff distance, volumetric similarity, and Euclidean distance. Together, these measures evaluate overlap, contour, volume, and location against expert manual segmentations. Our results indicate that HIPS-THOMAS and DeepThalamus outperformed the other automated methods in all metrics. However, manual segmentation retained high precision despite exhibiting greater inter-subject variance than the top-performing automated segmentation tools. The different metrics do not necessarily report the same order of quality, highlighting the need of using multiple metrics for evaluation segmentation quality.

neuroscience↗

Mapping the Human Visual Thalamus and its Cytoarchitectonic Subdivisions Using Quantitative MRI

The human lateral geniculate nucleus (LGN) of the visual thalamus is a key subcortical processing site for visual information analysis. A non-invasive assessment of the LGN and its functionally and microstructurally distinct magnocellular (M) and parvocellular (P) subdivisions in-vivo in humans is challenging, because of its small size and location deep inside the brain. Here we tested whether recent advances in high-field structural quantitative MRI (qMRI) can enable MR-based mapping of human LGN subdivisions. We employed ultra-high resolution 7 Tesla qMRI of a post-mortem human LGN specimen and high-resolution 7 Tesla in-vivo qMRI in a large participant sample. We found that a quantitative assessment of the LGN and a differentiation of its subdivisions was possible based on microstructure-informed MR-contrast alone. In both the post-mortem and in-vivo qMRI data, we identified two components of shorter and longer longitudinal relaxation time (T1) within the LGN that coincided with the known anatomical locations of a dorsal P and a ventral M subdivision, respectively. Through a subsequent ground truth histological examination of the same post-mortem LGN specimen, we showed that the observed T1 contrast pertains to cyto- and myeloarchitectonic differences between LGN subdivisions. These differences were based on cell and myelin density, but not on iron content. Our qMRI-based mapping strategy overcomes shortcomings of previous fMRI-based mapping approaches. It paves the way for an in-depth understanding of the function and microstructure of the LGN in humans. It also enables investigations into the selective contributions of LGN subdivisions to human behavior in health and disease. Significance StatementThe lateral geniculate nucleus (LGN) is a key processing site for the analysis of visual information. Due to its small size and deep location within the brain, non-invasive mapping of the LGN and its microstructurally distinct subdivisions in humans is challenging. Using quantitative MRI methods that are sensitive to underlying microstructural tissue features, we show that a differentiation of the LGN and its microstructurally distinct subdivisions is feasible in humans non-invasively. These findings are important because they open up novel opportunities to assess the hitherto poorly understood complex role of the LGN in human perception and cognition, as well as the contribution of selective LGN subdivision impairments to various clinical conditions including developmental dyslexia, glaucoma and multiple sclerosis.

neuroscience↗