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Glatard, T.

Publications and source records attributed to Glatard, T..

16 recordsLinked to original sources

Leveraging Segmentation Variability to Improve Brain Age Prediction

Analytical variability in neuroimaging pipelines contributes to concerns about reproducibility in the field. In structural MRI, different segmentation tools produce discrepant morphometric estimates that may influence downstream analyses, such as predictive modeling. We tested whether integrating several segmentation pipelines improves brain age prediction, and characterized the spatial and demographic structure of pipeline differences across several datasets. T1-weighted scans from five open-access datasets were processed with four widely-used structural segmentation pipelines. Brain age models were trained using single-pipeline features and compared with multi-pipeline aggregation strategies. Inter-pipeline variability was assessed across shared subcortical structures and examined in relation to age and sex. Integrating features across distinct segmentation frameworks improved predictive performance relative to individual pipelines, whereas aggregation within closely related software versions provided limited benefit. Variability was spatially structured and volumetric measures were often systematically associated with age and sex. These results suggest that segmentation differences reflect structured, demographically sensitive variation rather than random noise, and that multi-pipeline feature integration can enhance robustness in neuroimaging-based prediction.

neuroscience↗

Untrained Convolutional Neural Networks as Feature Extractors for Structural MRI

We demonstrate that features extracted from structural MRI using un-CNN, an untrained convolutional neural network, achieve predictive performance comparable to or exceeding that of state-of-the-art pretrained foundation models across three structural MRI datasets and three downstream tasks. Un-CNN extends a classical 3D CNN architecture with multi-channel inputs, a hierarchical encoder with multi-scale feature aggregation, and covariance pooling. Untrained CNNs circumvent several key limitations of trained models, including high computational cost and memory requirements, the need to distribute large model weights, risks of data leakage, and challenges in reproducibility.

neuroscience↗

From topography to connectome: Towards an integrated understanding of the resting brain

As the field expands from early research into the human connectome, there has been a fast expansion in the number of analytical approaches to study resting state functional MRI (rsfMRI) data. With increasing focus on individual differences, topographical brain maps of spatial organization have emerged in addition to traditional functional connectomes. Here, we developed a deep-learning model to embed maps of network topography and faithfully translate to individualized connectomes. Results confirmed the validity of the surface vision transformer based on reconstruction accuracy (0.73{+/-}0.09) and accurate topography-to-connectome translation (0.43{+/-}0.08). Importantly, translated connectomes retained identifiability and brain-cognition associations. These findings establish a direct mapping from spatial topography to connectomes that can be used to integrate scientific insights across rsfMRI sub-fields. This is an important step towards broadening our conceptualization of the connectome and supporting a broader integration of findings to inform a complete understanding of the human connectome. TeaserTranslating from spatial maps of brain organization to region-to-region connectomes retains shared individual differences.

bioinformatics↗

A Comparative Evaluation of Structural MRI Foundation Models for Brain Age Regression and Sex Classification

Foundation models pre-trained on large neuroimaging datasets offer a promising approach to overcome the limited sample sizes typical of clinical imaging studies, yet their generalization across diverse populations remains unclear. We present the first systematic benchmark of four publicly available structural MRI foundation models: AnatCL, BrainIAC, 3D-Neuro-SimCLR, and SwinBrain. Using T1-weighted MRIs from the Parkinson's Progression Markers Initiative (PPMI), Healthy Brain Network (HBN), and Nathan Kline Institute (NKI) datasets, we evaluate these models on sex classification, brain age prediction, and body mass index prediction, comparing against models trained from FreeSurfer-derived cortical thickness and cortical surface area features. Submitted models are evaluated using a standardized frozen feature probing framework. The evaluation methods are available in BrainFMBench, a living benchmark for structural brain MRI foundation models hosted on GitHub, where new models can be added through pull requests. Although some foundation models outperformed FreeSurfer on particular tasks and datasets, 3D-Neuro-SimCLR and AnatCL outperformed the baselines overall, with 3D-Neuro-SimCLR demonstrating the most consistent performance (with the notable exception of HBN sex classification). The remaining models did not consistently outperform the baselines, indicating that the advantage of learned representations over morphometric features was not consistent across datasets and tasks for these models. In addition, cross-model feature correlation analysis reveals that foundation model representations correlate differently with traditional cortical measurements. These findings position structural MRI foundation models, particularly 3D-Neuro-SimCLR and AnatCL, as promising avenues to boost the performance of predictive models in neuroimaging.

neuroscience↗

The practical impact of numerical variability on structural MRI measures of Parkinson's disease

Numerical variability is rarely quantified in neuroimaging despite many measures relying on subtle morphometric differences across individuals. We instrumented FreeSurfer 7.3.1, a widely used neuroimaging pipeline, to simulate numerical differences across computational environments, and used it to measure numerical variability in MRI analyses of Parkinsons disease patients and controls. In multiple cortical and subcortical regions, numerical variation reached nearly one-third of the population variability, altering statistical conclusions about group differences and clinical associations. To assess the impact of numerical noise in existing studies, we developed a practical tool that estimates the Numerical-Population Variability Ratio (NPVR) in a study, and propagates the resulting numerical variability to common statistics and associated p-values. By applying this framework to thirteen previously published studies reporting MRI measures in Parkinsons disease, we quantified the probability of numerically induced false positives and false negatives in the literature, highlighting a substantial impact of numerical variability on MRI measures of Parkinsons disease with an average significance-flip probability of 5% for cross-sectional studies and 10% for longitudinal studies. These results underscore the importance of systematically evaluating numerical stability in neuroimaging and provide a practical framework to do so.

bioinformatics↗

Numerical Variability of functional MRI Graph Measures

Network neuroscience provides a powerful framework for studying the mechanisms underlying brain-related diseases. As analyses become increasingly computational, ensuring their numerical reliability has become a critical challenge. Small perturbations introduced during processing can propagate through complex pipelines, leading to variability in outcomes and raising concerns about the reproducibility of reported findings. Addressing this issue requires systematic evaluation of pipeline stability to ensure results remain within acceptable numerical limits. While the numerical variability of structural imaging workflows has been investigated, with findings ranging from negligible to substantial, functional MRI (fMRI) pipelines and their derived graph measures remain underexplored. Without rigorous stability assessment, conclusions drawn from these measures may remain uncertain. We systematically evaluated the numerical variability of graph measures of functional connectivity derived from the widely-used fMRIPrep pipeline and compared it to population variability. The resulting Numerical-Population Variability Ratio (NPVR) values typically ranged from 0.1 to 0.2 for most graph metrics, indicating a measurable influence of numerical variability on network-derived outcomes. NPVR values varied across brain regions, thresholding choices, and confound regression strategies. These findings highlight numerical variability as an important factor in functional network studies, particularly when examining subtle effects or working with small sample sizes.

neuroscience↗

Styx: A multi-language API Generator for Command-Line Tools

In numerous scientific domains, established tools have often been developed with complex command-line interfaces. Such is the case for brain imaging and bioinformatics, making the use of powerful legacy tools in modern workflow paradigms challenging. We present (i) Styx, a compiler for generating language-native wrapper functions from static tool metadata, leading to seamless integration of command-line tools within the data science ecosystem. Alongside Styx, we have created (ii) NiWrap, a collection of more than 1900 neuroimaging command-line function descriptions as a proof-of-concept implementation. These interfaces, available in Python, R, and TypeScript (available at https://github.com/styx-api), significantly reduce the complexity of writing and interpreting software pipelines, particularly when composing workflows across packages with distinct API standards. The compiler architecture of Styx facilitates maintainability and portability across computing environments. As with all metadata-dependent infrastructure, creating sufficient metadata annotations remains a barrier to adoption. Accordingly, NiWrap demonstrates approaches that lower this barrier through direct source code extraction and LLM-assisted documentation parsing. Together, Styx and NiWrap offer a sustainable solution for interfacing diverse command-line tools with modern data science ecosystems. This modular approach enhances reproducibility and efficiency in pipeline development while ensuring portability across computing environments and programming languages.

bioinformatics↗

The impact of FreeSurfer versions on structural neuroimaging analyses of Parkinson's disease

Image processing software impacts the quantification of brain measures, playing an important role in the search for clinical biomarkers. We investigated the impact of the variability between FreeSurfer releases on the estimation of structural brain measures in Parkinsons disease (PD). Structural brain scans from 106 controls and 209 patients were analyzed with FreeSurfer versions 5.3, 6.0.1, and 7.3.2, including longitudinal data from 125 patients. First, we measured the differences in the estimation of volume, surface area, and cortical thickness between FreeSurfer versions. Second, we focused on the relationship between MRI-derived brain measures and group differences as well as disease severity clinical outcomes, which were evaluated both cross-sectionally and longitudinally. We found high software-induced variability in the estimation of all three structural measures, which impacted clinical outcomes. There were differences between software versions in group differences between patients and healthy controls in subcortical volume and vertex-wise cortical thickness. Software variability also impacted the estimated relationship between brain structure and disease severity in patients. Hence, software variability not only relates to the estimation of structural measures, but it also impacts clinically- relevant MRI measures. Our study provides insight into the reproducibility of structural neuroimaging studies in PD populations.

neuroscience↗

Registered report: Age-preserved semantic memory and the CRUNCH effect manifested as differential semantic control networks: an fMRI study

Semantic memory representations are generally well maintained in aging, whereas semantic control is thought to be more affected. To explain this phenomenon, this study tested the predictions of the Compensation-Related Utilization of Neural Circuits Hypothesis (CRUNCH), focusing on task demands in aging as a possible framework. The CRUNCH effect would manifest itself in semantic tasks through a compensatory increase in neural activation in semantic control network regions but only up to a certain threshold of task demands. This study compares 39 younger (20-35 years old) with 39 older participants (60-75 years old) in a triad-based semantic judgment task performed in an fMRI scanner while manipulating task demand levels (low versus high) through semantic distance. In line with the CRUNCH predictions, differences in neurofunctional activation and behavioral performance (accuracy and response times) were expected in younger versus older participants in the low-versus high-demand conditions, which should be manifested in semantic control Regions of Interest (ROIs). Our older participants had intact behavioral performance, as proposed in the literature for semantic memory tasks (maintained accuracy and slower response times (RTs)). Age-invariant behavioral performance in the older group compared to the younger one is necessary to test the CRUNCH predictions. The older adults were also characterized by high cognitive reserve, as our neuropsychological tests showed. Our behavioral results confirmed that our task successfully manipulated task demands: error rates, RTs and perceived difficulty increased with increasing task demands in both age groups. We did not find an interaction between age group and task demand, or a statistically significant difference in activation between the low- and high-demand conditions for either RTs or accuracy. As for brain activation, we did not find the expected age group by task demand interaction, or a significant main effect of task demand. Overall, our results are compatible with neural activation in the semantic network and the semantic control network, largely in frontotemporoparietal regions. ROI analyses demonstrated significant effects (but no interactions) of task demand in the left and right inferior frontal gyrus, the left posterior middle temporal gyrus, the posterior inferior temporal gyrus and the prefrontal gyrus. Overall, our test did not confirm the CRUNCH predictions.

neuroscience↗

Predicting Parkinson's disease progression using MRI-based white matter radiomic biomarker and machine learning: a reproducibility and replicability study

BackgroundThe availability of reliable biomarkers of Parkinsons disease (PD) progression is critical to the understanding of the disease and development of treatment options. Magnetic Resonance Imaging (MRI) provides a promising source of PD biomarkers, however, neuroimaging results have been shown to be markedly sensitive to analytical conditions and population sampling, which motivates investigations of their robustness. This study is part of a project to investigate the replicability of 11 structural MRI measures of PD identified in a recent review. ObjectiveThis paper attempts to reproduce (similar data, similar analysis) and replicate (variations in data and analysis) the design of the machine learning (ML) model described in [1] to predict PD progression from T1-weighted MRIs. MethodsWe used the Parkinsons Progression Markers Initiative dataset (PPMI, ppmi-info.org) used in [1] and we followed as closely as possible the original methods. We also investigated slight methodological variations in cohort selection, feature extraction, ML model design, and evaluation techniques. ResultsThe Area under the ROC Curve (AUC) achieved by our model closely reproducing the original study remained lower than 0.5. Across all tested models, we obtained a peak AUC of 0.685, which is better than chance performance but remained lower than the AUC value of 0.795 reported in [1]. ConclusionWe managed to train a model that predicts disease progression with a performance better than chance on a cohort extracted from the PPMI dataset, using methods adapted from [1]. However, the performance of this model remains substantially lower than the one reported in [1]. Our difficulties to reproduce or replicate the original work are likely explained by the relatively low sample size in the original study. We provide recommendations on how to improve the reproducibility of MRI-based ML models of PD in the future.

neuroscience↗

Longitudinal brain structure changes in Parkinson's disease: a replication study

ContextAn existing major challenge in Parkinsons disease (PD) research is the identification of biomarkers of disease progression. While Magnetic Resonance Imaging (MRI) is a potential source of PD biomarkers, none of the MRI measures of PD are robust enough to warrant their adoption in clinical research. This study is part of a project that aims to replicate 11 PD studies reviewed in a recent survey (JAMA neurology, 78(10) 2021) to investigate the robustness of PD neuroimaging findings to data and analytical variations. ObjectiveThis study attempts to replicate the results in Hanganu et al. (Brain, 137(4) 2014) using data from the Parkinsons Progression Markers Initiative (PPMI). MethodsUsing 25 PD subjects and 18 healthy controls, we analyzed the rate of change of cortical thickness and of the volume of subcortical structures, and we measured the relationship between MRI structural changes and cognitive decline. We compared our findings to the results in the original study. ResultsSimilarly to the original study, PD patients with mild cognitive impairment (MCI) exhibited increased cortical thinning over time compared to patients without MCI in the right middle temporal gyrus, insula, and precuneus. (2) The rate of cortical thinning in the left inferior temporal and precentral gyri in PD patients correlated with the change in cognitive performance. (3) There were no group differences in the change of subcortical volumes. (4) We did not find a relationship between the change in subcortical volumes and the change in cognitive performance. ConclusionDespite important differences in the dataset used in this replication study, and despite differences in sample size, we were able to partially replicate the original results. We produced a publicly available reproducible notebook allowing researchers to further investigate the reproducibility of the results in Hanganu et al. (2014) when more data becomes available in PPMI.

neuroscience↗

NeuroCI: Continuous Integration of Neuroimaging Results Across Software Pipelines and Datasets

--Neuroimaging study results can vary significantly depending on the datasets and processing pipelines utilized by researchers to run their analyses, contributing to reproducibility issues. These issues are compounded by the fact that there are a large variety of seemingly equivalent tools and methodologies available to researchers for processing neuroimaging data. Here we present NeuroCI, a novel software framework that allows users to evaluate the variability of their results across multiple pipelines and datasets. NeuroCI makes use of Continuous Integration (CI), a software engineering technique, to facilitate the reproducibility of computational experiments by launching a series of automated tests when code or data is added to a repository. However, unlike regular CI services, our CI-based framework uses distributed computation and storage to meet the large memory and storage requirements of neuroimaging pipelines and datasets. Moreover, the frameworks modular design enables it to continuously ingest pipelines and datasets provided by the user, and to compute and visualize results across the multiple different pipelines and datasets. This allows researchers and practitioners to quantify the variability and reliability of results in their domain across a large range of computational methods.

bioinformatics↗

BigBrainWarp: Toolbox for integration of BigBrain 3D histology with mutlimodal neuroimaging

AO_SCPLOWBSTRACTC_SCPLOWNeuroimaging stands to benefit from emerging ultrahigh-resolution histological atlases of the human brain; the first of which is "BigBrain". Ongoing research aims to characterise regional differentiation of cytoarchitecture with BigBrain and to optimise registration of BigBrain with standard neuroimaging templates. Together, this work paves the way for multi-scale investigations of brain organisation. However, working with BigBrain can present new challenges for neuroimagers, including dealing with cellular resolution neuroanatomy and complex transformation procedures. To simplify workflows and support adoption of best practices, we developed BigBrainWarp, a toolbox for integration of BigBrain with multimodal neuroimaging. The primary BigBrainWarp function wraps multiple state-of-the-art deformation matrices into one line of code, allowing users to easily map data between BigBrain and standard MRI spaces. Additionally, the toolbox contains ready-to-use cytoarchitectural features to improve accessibility of histological information. The present article discusses recent contributions to BigBrain-MRI integration and demonstrates the utility of BigBrainWarp for further investigations.

neuroscience↗

Data Augmentation Through Monte Carlo Arithmetic Leads to More Generalizable Classification in Connectomics

Machine learning models are commonly applied to human brain imaging datasets in an effort to associate function or structure with behaviour, health, or other individual phenotypes. Such models often rely on low-dimensional maps generated by complex processing pipelines. However, the numerical instabilities inherent to pipelines limit the fidelity of these maps and introduce computational bias. Monte Carlo Arithmetic, a technique for introducing controlled amounts of numerical noise, was used to perturb a structural connectome estimation pipeline, ultimately producing a range of plausible networks for each sample. The variability in the perturbed networks was captured in an augmented dataset, which was then used for an age classification task. We found that resampling brain networks across a series of such numerically perturbed outcomes led to improved performance in all tested classifiers, preprocessing strategies, and dimensionality reduction techniques. Importantly, we find that this benefit does not hinge on a large number of perturbations, suggesting that even minimally perturbing a dataset adds meaningful variance which can be captured in the subsequently designed models. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=65 SRC="FIGDIR/small/423084v2_ufig1.gif" ALT="Figure 1"> View larger version (17K): org.highwire.dtl.DTLVardef@bccd23org.highwire.dtl.DTLVardef@13fcfe1org.highwire.dtl.DTLVardef@68e987org.highwire.dtl.DTLVardef@1bbada9_HPS_FORMAT_FIGEXP M_FIG This paper demonstrates how Monte Carlo Arithmetic, a dataagnostic perturbation technique, can be used for dataset augmentation during the generation of structural connectomes and improve downstream phenotypic prediction. C_FIG

neuroscience↗

Numerical Instabilities in Analytical Pipelines Lead to Large and Meaningful Variability in Brain Networks

The analysis of brain-imaging data requires complex processing pipelines to support findings on brain function or pathologies. Recent work has shown that variability in analytical decisions, small amounts of noise, or computational environments can lead to substantial differences in the results, endangering the trust in conclusions1-7. We explored the instability of results by instrumenting a connectome estimation pipeline with Monte Carlo Arithmetic8,9 to introduce random noise throughout. We evaluated the reliability of the connectomes, their features10,11, and the impact on analysis12,13. The stability of results was found to range from perfectly stable to highly unstable. This paper highlights the potential of leveraging induced variance in estimates of brain connectivity to reduce the bias in networks alongside increasing the robustness of their applications in the classification of individual differences. We demonstrate that stability evaluations are necessary for understanding error inherent to brain imaging experiments, and how numerical analysis can be applied to typical analytical workflows both in brain imaging and other domains of computational science. Overall, while the extreme variability in results due to analytical instabilities could severely hamper our understanding of brain organization, it also leads to an increase in the reliability of datasets.

neuroscience↗

Objective Evaluation of Multiple Sclerosis Lesion Segmentation using a Data Management and Processing Infrastructure

We present a study of multiple sclerosis segmentation algorithms conducted at the international MICCAI 2016 challenge. This challenge was operated using a new open-science computing infrastructure. This allowed for the automatic and independent evaluation of a large range of algorithms in a fair and completely automatic manner. This computing infrastructure was used to evaluate thirteen methods of MS lesions segmentation, exploring a broad range of state-of-the-art algorithms, against a high-quality database of 53 MS cases coming from four centers following a common definition of the acquisition protocol. Each case was annotated manually by an unprecedented number of seven different experts. Results of the challenge highlighted that automatic algorithms, including the recent machine learning methods (random forests, deep learning, ...), are still trailing human expertise on both detection and delineation criteria. In addition, we demonstrate that computing a statistically robust consensus of the algorithms performs closer to human expertise on one score (segmentation) although still trailing on detection scores.

neuroscience↗