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Poline, J.-B.

Publications and source records attributed to Poline, J.-B..

At least 19 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↗

Who Funds Open Data Sharing? Analysis of data availability statements in biomedical publications

Open data sharing is increasingly mandated by research funders, journals, and institutions, yet large-scale compliance measurement remains challenging. We analyzed 951,949 open access biomedical research articles published between January 2024 and June 2025 using a dual-source pipeline: PDF-based text extraction (MinerU) where PDFs were available and PMC XML otherwise, followed by algorithmic detection of data sharing statements (oddpub v7.2.3), enriched with funder, journal, and institutional metadata from OpenAlex. The corpus included 294,172 PDF-covered articles (30.9%) and 657,777 XML-only articles (69.1%). We found an over-all open data rate of 8.7%, rising to 11.7% among funder-linked articles (those with at least one funder identified in the metadata). Rates varied more than tenfold across the research ecosystem: leading major funders reached observed open data rates of 20-24%, while top journals reached observed rates of 70-86%, with corrected estimates as high as 92.9% (Nature Genetics) after adjusting for XML-only coverage limitations. PDF-based detection identified approximately 52% more data sharing statements than XML-based methods on the same articles. These observed rates differ markedly across funders and journals, and current overall sharing remains far below universal compliance. These patterns provide an empirical baseline against which future policy changes can be measured. An interactive dashboard at https://www.opensciencemetrics.org enables stakeholders to explore and benchmark these results.

scientific communication and education↗

When Can Brain Connectivity Track the Working Mind? A Large-Scale Benchmark of Dynamic Functional Connectivity Across Cognitive Paradigms

Dynamic functional connectivity (dFC) -- the time-varying re-configuration of brain network interactions -- has become a widely adopted method for studying how neural dynamics reflect ongoing cognition. Yet a fundamental question remains unresolved: can dFC reliably track when a person is cognitively engaged, and if not, why does it fail? Here, we address this question through a large-scale benchmark of seven widely used dFC methods, evaluating how well each predicts task presence across 16 fMRI datasets encompassing over 1,500 participants and 28 distinct experimental settings, complemented by realistic simulated data. Across experimental data, dFC-based tracking of cognitive engagement was unreliable in many cases: most method-experiment combinations performed near chance, and no single method succeeded across all contexts. This failure, however, was not uniform. Both experimental and simulated data showed that decoding performance varied systematically with three interacting factors -- experimental design, data quality, and the choice of dFC method -- rather than depending on dFC features alone. Critically, we identify specific experimental design conditions associated with more reliable tracking: paradigms with longer, more regular task blocks and fewer task-rest transitions were substantially more decodable, while data quality independently influenced performance across methods. These findings offer actionable principles for when dFC can -- and cannot -- be expected to serve as a reliable marker of underlying cognitive states.

neuroscience↗

Nipoppy: A framework for standardizing neuroimaging studies to facilitate international derived-data sharing

Neuroimaging data management and processing are tedious and error-prone, prompting reproducibility concerns. Globally, studies with heterogeneous infrastructure and governance policies lead to eclectic data processing and sharing, necessitating standardization of data workflows to ensure reusability and comparability of multi-centric datasets. The Nipoppy neuroinformatics framework facilitates such standardization by combining specification, protocol, and software to manage study-level data workflows. With its adoption, researchers can share standardized, derived datasets enabling efficient, reproducible, and inclusive research.

bioinformatics↗

Open neuroinformatics infrastructure ecosystem for federated multisite studies

Despite growing understanding of the benefits of having Findable, Accessible, Interoperable, and Reusable (FAIR) data, many datasets still cannot be shared. Federated analysis methods can enable multisite studies that do not require the sharing of participant-level information. However, there are many practical hurdles that prevent the large-scale adoption of federated methods. We discuss challenges related to cross-site data preparation for federated learning, present solutions offered by recent neuroinformatics projects, and showcase an example of tool integration applied to neurodegenerative disease data.

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↗

Deep Learning for Cognitive Task Presence Prediction from Dynamic Functional Connectivity

Dynamic functional connectivity (dFC) studies the time-varying coordination between brain regions measured with fMRI and is a potential biomarker for understanding cognitive dynamics and tracking the development of neurological disorders. However, a critical methodological challenge lies in the variability of dFC estimates across different dFC assessment methods, raising concerns about the reliability and interpretation of downstream findings. While deep learning (DL) models have demonstrated the ability to capture traditionally inaccessible data patterns in many disciplines, they encounter challenges when applied to neuroimaging data. For instance, the high dimensionality, noise, and temporal complexity inherent in dFC makes it challenging for DL models to extract meaningful and interpretable insights. In this study, we investigated how DL architectures can be developed and adapted to predict task presence over time from task-based dFC data, and additionally, how the choice of dFC assessment method influences the predictive performance of DL models. We developed and compared a convolutional neural network (CNN), a node-level classification graph convolutional network (GCN), and a graph-level classification GCN based on their ability to predict time points at which subjects were performing a cognitive task or at rest. In our study, the results indicate that both DL model architecture and dFC estimation methodology significantly impact task presence prediction capacity, while the specific task paradigm had minimal influence out of the limited types that were explored. This work offers a powerful benchmark for understanding the dynamics of underlying task-driven cognitive state transitions and the analytical flexibility limitations of dFC estimation methods and DL architectures.

neuroscience↗

Clinical profile impacts the replicability of multivariate brain-behavioural associations

Recent work suggests that thousands of individuals are required in multivariate brain-behaviour analyses to obtain consistently replicable results. Some believe, however, that smaller sample sizes may be sufficient if specific subpopulations are targeted. We investigate how sample size and cohort composition influence the replicability of Canonical Correlation Analysis (CCA) results using the UK Biobank (N=40,514). We apply CCA to diffusion-weighted magnetic resonance imaging (dMRI) phenotypes and cognitive assessment test scores. We define four participant cohorts based on clinical profile and find that, across all cohorts, sample sizes of {approx}500 are needed to obtain replicable canonical correlations and variable loadings. The most targeted cohort (comprising individuals with a history of psychoactive substance use) requires much fewer samples to achieve similar or greater correlations than the other cohorts. Our findings support the idea that moderate sample sizes from targeted cohorts can be sufficient for obtaining replicable brain-behaviour associations.

neuroscience↗

NiCLIP: Neuroimaging contrastive language-image pretraining model for predicting text from brain activation images

Predicting cognitive processes from brain activation maps has remained an open question within the neuroscience community for many years. Meta-analytic functional decoding methods aim to tackle this issue by providing a quantitative estimation of behavioral profiles associated with specific brain regions. Existing methods face intrinsic challenges in neuroimaging meta-analysis, particularly in consolidating textual information from publications, as they rely on limited metrics that do not capture the semantic context of the text. The combination of large language models (LLMs) with advanced deep contrastive learning models (e.g., CLIP) for aligning text with images has revolutionized neuroimaging meta-analysis, potentially offering solutions to functional decoding challenges. In this work, we present NiCLIP, a contrastive language-image pretrained model that predicts cognitive tasks, concepts, and domains from brain activation patterns. We leveraged over 23,000 neuroscientific articles to train a CLIP model for text-to-brain association. Evaluation of NiCLIP predictions revealed that performance is optimized when using full-text articles instead of abstracts, as well as a curated cognitive ontology with precise task-concept-domain mappings. Furthermore, domain-specific fine-tuned LLMs (e.g., BrainGPT models) show numerically similar performance to their base LLM counterparts. Our results indicated that NiCLIP accurately predicts cognitive tasks from group-level activation maps provided by the Human Connectome Project across multiple domains (e.g., emotion, language, motor) and precisely characterizes the functional roles of specific brain regions, including the amygdala, hippocampus, and temporoparietal junction. However, NiCLIP showed limitations with noisy subject-level activation maps. NiCLIP represents a significant advancement in quantitative functional decoding for neuroimaging, offering researchers a powerful tool for hypothesis generation and scientific discovery.

neuroscience↗

Advancing image-based meta-analysis for fMRI: A framework for leveraging NeuroVault data

Image-based meta-analysis (IBMA) is a powerful method for synthesizing results from various fMRI studies. However, challenges related to data accessibility and the lack of available tools and methods have limited its widespread use. This study examined the current state of the NeuroVault repository and developed a comprehensive framework for selecting and analyzing neuroimaging statistical maps within it. By systematically assessing the quality of NeuroVault's data and implementing novel selection and meta-analysis techniques, we demonstrated the repository's potential for IBMA. We created a multi-stage selection framework that includes preliminary, heuristic, and manual image selection methods. We conducted meta-analyses for three distinct domains: working memory, motor, and emotion processing. The results from the three manual IBMA approaches closely resembled reference maps from the Human Connectome Project. Importantly, we found that while manual selection provides the most precise results, heuristic methods can serve as robust alternatives, especially for domains that include a heterogeneous set of fMRI tasks and contrasts, such as emotion processing. Additionally, we evaluated five different meta-analytic estimator methods to assess their effectiveness in handling spurious images. For domains characterized by heterogeneous tasks, employing a robust estimator (e.g., median) is essential. This study is the first to present a systematic approach for implementing IBMA using the NeuroVault repository. We introduce an accessible and reproducible methodology that allows researchers to make the most of NeuroVault's extensive neuroimaging resources, potentially fostering greater interest in data sharing and future meta-analyses utilizing NeuroVault data.

neuroscience↗

Meta all the way down: An overview of neuroimaging meta-analyses

Meta-analyses are invaluable tools for navigating the rapidly expanding scientific literature. Given their high value, ensuring the quality of meta-analyses is paramount. We conducted a multifaceted overview, examining each step in a manual neuroimaging meta-analysis on a large scale. We used four novel datasets comprising over 14,000 papers, including fMRI meta-analyses, fMRI studies, studies included in meta-analyses, and studies associated with image data on NeuroVault. Regarding successes, two-thirds of meta-analyses stated that they followed PRISMA guidelines, and 65% included a flowchart describing their inclusion process. We point out several areas for improvement. Pre-registration was fairly rare (20%), and only half listed their exact search strategy. There could be a location bias in which papers are included, and many did not include enough studies to be robust against publication bias (68% of meta analyses have less than 30 studies included). We also offer ideas for future directions. As image based meta-analysis is the gold standard, we have indicated which topics have the most image data available. The potential redundancy of topics can be visualized in our paper, and we recommend future meta-analyses be in conversation with past ones by citing and discussing previous similar work. By addressing these findings, the neuroimaging community can collectively improve the field of neuroimaging meta-analyses.

neuroscience↗

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↗

Investigation of the effect of physiological factors on resting-state and task-based functional connectivity

Understanding the brains functional network through functional connectivity (FC) is crucial for gaining deeper insights into brain functional mechanism and identifying a potential biomarker for diagnosing neurological disorders. Despite the development of various FC measures, their reliability under different conditions remains under-explored. Moreover, physiological noise can obscure true neural activity, and accordingly, introduce errors into FC patterns. This issue necessitates further investigation. In this study, we evaluate and compare the performance of various methods using Local Field Potential and Blood-Oxygen-Level-Dependent signals across different conditions. We also examine the impact of physiological artifacts on BOLD-FC results. Our comprehensive assessment covers multiple modalities of brain signals, diverse task paradigms, and varying noise levels. Our findings reveal that while Granger Causality-based methods exhibit significant limitations, particularly with BOLD data, multivariate techniques (e.g. partial correlation) demonstrate greater robustness in distinguishing between different types of connections within the network. Notably, our results indicate that physiological artifacts substantially affect FC values, leading to erroneous connectivity estimates, especially with bivariate methods. This research offers a foundational analysis of the effects of physiological artifacts on FC results and provides valuable insights for future studies.

neuroscience↗

Three Subtypes Of Autism Spectrum Disorder With Transcriptomic Signatures Derived From Morphometric Similarity Networks

Autism spectrum disorder (ASD) is a prevalent and highly heterogeneous neurodevelopmental disorder. Previous studies have attempted to identify ASD subgroups by analyzing isolated cortical structural features. However, these studies have not considered the relationship between multiple structural features, which provide information on the structural organization of the brain. Morphometric similarity network (MSN), a structural brain network contributed by multiple anatomical features (gray matter volume, mean cortical thickness, surface area, mean curvature, Gaussian curvature, curvature index, and fold index), strongly relates to cytoarchitectonic and genomic measures of histological similarity between cortical areas. We applied K-means clustering on MSN from 236 individuals with ASD and identified three subtypes. Subtype-1 showed relatively similar MSN values with typically developmental individuals (TD). Subtype-2 showed higher morphometric similarities in the lateral frontal and temporal cortical regions and lower in anterior prefrontal and occipital regions compared to TD. These patterns were the opposite in subtype-3. Behaviorally, subtype-3 had more severe verbal and social deficits compared to subtype-2. The weaker resting-state functional connectivity (rs-FC) between the language and salience networks was observed between subtype-2 and TD. Subtype-3 had stronger rs-FC between salience and default mode networks (DMN), between frontoparietal and visual networks, and between language and dorsal attention networks, while weaker rs-FC within DMN, within sensorimotor, and within salience networks. In addition, genes with expression patterns associated with regional MS changes in ASD subtypes were functionally enriched in neuron-specific biological processes related to nervous system development, synaptic signaling and chromatin organization. These genes were particularly enriched in GABAergic neurons, glutamatergic neurons, astrocytes and microglia. Taken together, our findings suggest the existence of different neuroanatomical subtypes based on multiple anatomical features in ASD with distinct transcriptomic signatures and functional connectome patterns.

neuroscience↗

Mining the neuroimaging literature

Automated analysis of the biomedical literature (literature-mining) offers a rich source of insights. However, such analysis requires collecting a large number of articles and extracting and processing their content. This task is often prohibitively difficult and time-consuming. Here, we provide tools to easily collect, process and annotate the biomedical literature. In particular, pubget is an efficient and reliable command-line tool for downloading articles in bulk from PubMed Central, extracting their contents and meta-data into convenient formats, and extracting and analyzing information such as stereotactic brain coordinates. Labelbuddy is a lightweight local application for annotating text, which facilitates the extraction of complex information or the creation of ground-truth labels to validate automated information extraction methods. Further, we describe repositories where researchers can share their analysis code and their manual annotations in a format that facilitates re-use. These resources can help streamline text-mining and meta-science projects and make text-mining of the biomedical literature more accessible, effective, and reproducible. We describe a typical workflow based on these tools and illustrate it with several example projects.

neuroscience↗

Meta-analytic decoding of the cortical gradient of functional connectivity

Macroscale gradients have emerged as a central principle for understanding functional brain organization. Previous studies have demonstrated that a principal gradient of connectivity in the human brain exists, with unimodal primary sensorimotor regions situated at one end and transmodal regions associated with the default mode network and representative of abstract functioning at the other. The functional significance and interpretation of macroscale gradients remains a central topic of discussion in the neuroimaging community, with some studies demonstrating that gradients may be described using meta-analytic functional decoding techniques. However, additional methodological development is necessary to fully leverage available meta-analytic methods and resources and quantitatively evaluate their relative performance. Here, we conducted a comprehensive series of analyses to investigate and improve the framework of data-driven, meta-analytic methods, thereby establishing a principled approach for gradient segmentation and functional decoding. We found that a two-segment solution determined by a k-means segmentation approach and an LDA-based meta-analysis combined with the NeuroQuery database was the optimal combination of methods for decoding functional connectivity gradients. Finally, we proposed a method for decoding additional components of the gradient decomposition. The current work aims to provide recommendations on best practices and flexible methods for gradient-based functional decoding of fMRI data.

neuroscience↗

On the variability of dynamic functional connectivity assessment methods

Dynamic functional connectivity (dFC) has become an important measure for understanding brain function and as a potential biomarker. However, various methodologies have been developed for assessing dFC, and it is unclear how the choice of method affects the results. In this work, we aimed to study the results variability of commonly-used dFC methods. We implemented seven dFC assessment methods in Python and used them to analyze fMRI data of 395 subjects from the Human Connectome Project. We measured the pairwise similarity of dFC results using several similarity metrics in terms of overall, temporal, spatial, and inter-subject similarity. Our results showed a range of weak to strong similarity between the results of different methods, indicating considerable overall variability. Surprisingly, the observed variability in dFC estimates was comparable to the expected natural variation over time, emphasizing the impact of methodological choices on the results. Our findings revealed three distinct groups of methods with significant inter-group variability, each exhibiting distinct assumptions and advantages. These findings highlight the need for multi-analysis approaches to capture the full range of dFC variation. They also emphasize the importance of distinguishing neural-driven dFC variations from physiological confounds, and developing validation frameworks under a known ground truth. To facilitate such investigations, we provide an open-source Python toolbox that enables multi-analysis dFC assessment. This study sheds light on the impact of dFC assessment analytical flexibility, emphasizing the need for careful method selection and validation, and promoting the use of multi-analysis approaches to enhance reliability and interpretability of dFC studies.

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↗