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Kebiri, H.

Publications and source records attributed to Kebiri, H..

6 recordsLinked to original sources

Domain shifts in infant brain diffusion MRI: Quantification and mitigation for fODF estimation

The accurate estimation of fiber orientation distributions (fODFs) in diffusion magnetic resonance imaging (MRI) is crucial for understanding early brain development and its potential disruptions. While deep learning (DL) models have shown promise in fODF estimation from neonatal diffusion MRI (dMRI) data, the out-of-domain (OOD) performance of these models remains largely unexplored, especially under diverse domain shift scenarios. This study evaluated the robustness of three state-of-the-art DL architectures--MLP-based, Transformer-based, and U-Net/CNN-based--on fODF predictions derived from diffusion MRI data. Using 488 subjects from the developing Human Connectome Project (dHCP) and the Baby Connectome Project (BCP) datasets, we reconstructed reference fODFs from the full dMRI series using single-shell three-tissue constrained spherical deconvolution (SS3T-CSD) and multi-shell multi-tissue CSD (MSMT-CSD) to generate reference fODF reconstructions for model training, and systematically assessed the impact of age, scanner/protocol differences, and input dimensionality on model performance. Our findings reveal that U-Net consistently outperformed other models when fewer diffusion gradient directions were used, particularly with the SS3T-CSD-derived ground truth, which showed superior performance in capturing crossing fibers. However, as the number of input diffusion gradient directions increased, MLP and the transformer-based model exhibited steady gains in accuracy. Nevertheless, performance nearly plateaued from 28 to 45 input directions in all models. Age-related domain shifts were found to be less pronounced in late developmental stages (late neonates, and babies), with SS3T-CSD demonstrating greater robustness to variability compared to MSMT-CSD. To address inter-site domain shifts, we implemented two adaptation strategies: the Method of Moments (MoM) and fine-tuning. Fine-tuning consistently yielded superior results, with U-Net benefiting the most from increased target subjects. This study represents the first systematic evaluation of OOD settings in deep learning applications to fODF estimation, providing critical insights into model robustness and adaptation strategies for diverse clinical and research applications.

bioinformatics↗

Functional organization of the neonatal thalamus across development depicted by functional MRI

The thalamus is a central component of the brain that is involved in a variety of functions, from sensory processing to high-order cognition. Its structure and function in the first weeks of extrauterine life, including its connections to different cortical and subcortical areas, have not yet been widely explored. Here, we used resting state functional magnetic resonance imaging data of 730 newborns from the developing Human Connectome Project to study the functional organization of the thalamus from 37 to 44 post-conceptual weeks. We introduce KNIT: K-means for Nuclei in Infant Thalamus. The framework employs a highly granular vector space of 40 features, each corresponding to functional connectivity to a brain region, using k-means clustering and uncertainty quantification through bootstrapping to delineate thalamic units. Although the different clusters showed common patterns of increased connectivity to the superior temporal gyrus, the parietal, and the frontal cortex, implying an expected decrease in specialization at that age, they also show some specificity. That is, a pulvinar unit was identified, similar to the adult thalamus. Ventrolateral motor and medial salience units were also highlighted. The latter appeared around 41 weeks of age, while the former showed at least from 37 weeks, but had a decrease in volume through age, replaced mostly by a dominant dorsal thalamic unit. We also observed an increase in clustering robustness and in hemispheric bilateral symmetry with age, suggesting more specialized functional units. We also found a burst in global thalamic connectivity around 41 weeks. Finally, we demonstrate the benefits of this method in terms of granularity compared to the more conventional winner-takes-all approach.

neuroscience↗

Eye-Opening Advances: Automated 3D Segmentation, Key Biomarkers Extraction, and the First Large-Scale MRI Eye Atlas.

In this study we introduce an automated 3D segmentation of the healthy human adult eye and orbit from Magnetic Resonance Images, to improve ophthalmic diagnostics and treatments. Past efforts primarily focused on small sample sizes and varied imaging modalities. Here, we leverage a large-scale dataset of T1-weighted MRI of 1245 subjects and the use of the deep learning-based nnU-Net for MR-Eye segmentation tasks. The results showcase robust and accurate 3D segmentations of lens, globe, optic nerve, rectus muscles, and orbital fat. We also present the automated estimation of key ophthalmic morphometry biomarkers such as axial length and volumetry, while benchmarking correlations between body mass index and eye structure volumes. Quality control protocols are introduced through the pipeline to ensure the reliability of the segmented large-scale data, further enhancing the applicability of our algorithm in clinical research. As major outcome we provide the first large-scale unbiased eye atlases (female, male and combined) towards standardization of spatial normalization tools for MR-Eye.

bioengineering↗

TBSS++: A novel computational method for Tract-Based Spatial Statistics

Diffusion-weighted magnetic resonance imaging (dMRI) is widely used to assess the brain white matter. One of the most common computations in dMRI involves cross-subject tract-specific analysis, whereby dMRI-derived biomarkers are compared between cohorts of subjects. The accuracy and reliability of these studies hinges on the ability to compare precisely the same white matter tracts across subjects. This is an intricate and error-prone computation. Existing computational methods such as Tract-Based Spatial Statistics (TBSS) suffer from a host of shortcomings and limitations that can seriously undermine the validity of the results. We present a new computational framework that overcomes the limitations of existing methods via (i) accurate segmentation of the tracts, and (ii) precise registration of data from different subjects/scans. The registration is based on fiber orientation distributions. To further improve the alignment of cross-subject data, we create detailed atlases of white matter tracts. These atlases serve as an unbiased reference space where the data from all subjects is registered for comparison. Extensive evaluations show that, compared with TBSS, our proposed framework offers significantly higher reproducibility and robustness to data pertur-bations. Our method promises a drastic improvement in accuracy and reproducibility of cross-subject dMRI studies that are routinely used in neuroscience and medical research.

bioengineering↗

Deep learning microstructure estimation of developing brains from diffusion MRI: a newborn and fetal study

Diffusion-weighted magnetic resonance imaging (dMRI) is widely used to assess the brain white matter. Fiber orientation distribution functions (FODs) are a common way of representing the orientation and density of white matter fibers. However, with standard FOD computation methods, accurate estimation of FODs requires a large number of measurements that usually cannot be acquired for newborns and fetuses. We propose to overcome this limitation by using a deep learning method to map as few as six diffusion-weighted measurements to the target FOD. To train the model, we use the FODs computed using multi-shell high angular resolution measurements as target. Extensive quantitative evaluations show that the new deep learning method, using significantly fewer measurements, achieves comparable or superior results to standard methods such as Constrained Spherical Deconvolution. We demonstrate the generalizability of the new deep learning method across scanners, acquisition protocols, and anatomy on two clinical datasets of newborns and fetuses. Additionally, we compute agreement metrics within the HARDI newborn dataset, and validate fetal FODs with post-mortem histological data. The results of this study show the advantage of deep learning in inferring the microstructure of the developing brain from in-vivo dMRI measurements that are often very limited due to subject motion and limited acquisition times, but also highlight the intrinsic limitations of dMRI in the analysis of the developing brain microstructure. These findings, therefore, advocate for the need for improved methods that are tailored to studying the early development of human brain.

bioinformatics↗

Through-plane super-resolution with autoencoders in diffusion magnetic resonance imaging of the developing human brain

Fetal brain diffusion magnetic resonance images are often acquired with a lower through-plane than in-plane resolution. This anisotropy is often overcome by classical upsampling methods such as linear or cubic interpolation. In this work, we employ an unsupervised learning algorithm using an autoencoder neural network to enhance the through-plane resolution by leveraging a large amount of data. Our framework, which can also be used for slice outliers replacement, overperformed conventional interpolations quantitatively and qualitatively on pre-term newborns of the developing Human Connectome Project. The evaluation was performed on both the original diffusion-weighted signal and on the estimated diffusion tensor maps. A byproduct of our autoencoder was its ability to act as a denoiser. The network was able to generalize to fetal data with different levels of motion and we qualitatively showed its consistency, hence supporting the relevance of pre-term datasets to improve the processing of fetal brain images.

bioinformatics↗