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Boccard, J.

Publications and source records attributed to Boccard, J..

2 recordsLinked to original sources

A benchmarking workflow for assessing the reliability of batch correction methods

One of the most pervasive challenges in large-scale untargeted metabolomics is short and long-term analytical variability introducing the necessity of batch effect correction. In this context, several strategies and methods have been developed to limit those effects, either by monitoring the data generation process to maximize reproducibility or by applying post-analysis data correction. Different evaluation frameworks, either assessing the degree of bias in the data through visual tools or quantitative indicators, or evaluating the prediction performance of known biomarkers, were also proposed. However, there is currently no clear consensus on how to evaluate batch correction methods. This work offers a strategy to assess multiple dimensions of batch correction efficiency within a comprehensive and reliable framework, designed to assess the effectiveness and reliability of batch correction methods. Based on Mahalanobis Conformity Index (MCI), it provides a multivariate and covariance-aware metric to quantify within- and between-batch variability. Additionally, it combines visualization techniques (Principal Component Analysis (PCA) and Multivariate INTegrative (MINT) PCA) with numerical indicators (batch dispersion, Coefficient of Variation), supporting both multidimensional and metabolite-specific evaluations. Lastly, this novel approach integrates statistical tools alongside chemistry-based metrics for method overfitting and overcorrection assessment. Applied within a use case for comparing LOESS-based and ComBat correction methods, the present workflow provided a structured approach to systematically assess the reliability of batch corrections, ensuring both data intercomparability and biological relevance in metabolomics studies. Author summaryThe assessment of batch correction is a challenge in metabolomics, where there is no consensus for a define strategy, making it a complex task. However, knowing the impact of batch correction on the datasets and consecutive possible impact on downstream statistical analyses, providing a reliable framework for its assessment is a cornerstone for reproducible results. The objective of the present work was to provide a framework and a set of interpretation tools combining numerical indicators, as well as diagnostic plots, for assessing the reliability of batch correction methods. We introduced a robust evaluation framework centered on the Mahalanobis Conformity Index, providing a multivariate and covariance-aware metric to quantify within- and between-batch variability. By coupling this index with visual tools (based on Principal Component Analysis (PCA) and Multivariate INTegrative (MINT) PCA), as well as compound-level diagnostics, we enabled a fine-grained and interpretable comparison of correction strategies, highlighting their strengths and potential pitfalls.

bioinformatics↗

Neurotoxicity of Propylene Glycol Butyl Ether: Multiomic Evidence from Human BrainSpheres

Exposure to solvents may contribute to the development of neurodevelopmental and neurodegenerative diseases. Glycol ethers consist in a widely used class of organic solvents leading to workers and consumers exposure via many different applications. Ethylene glycol ethers are gradually being replaced by propylene glycol ethers thought to be less toxic. However, their neurotoxicity is not systematically assessed prior to placing them on the market. Therefore, this study investigated the potential neurotoxicity of propylene glycol butyl ether (PGBE) for which no official occupational limit has been established. To this aim, new approach methodologies have been used. Human induced pluripotent stem cells-derived BrainSpheres model was exposed to PGBE and to its main metabolite, 2-butoxypropanoic acid (2BPA). An integrative multiomic approach (transcriptomics, proteomics, metabolomics and lipidomics) was adopted to assess molecular alterations, derive benchmark concentrations and define potential mechanisms of action. PGBE was neurotoxic at occupationally relevant exposure concentrations. This was shown for the first time in human cells. And, although PGBE was more cytotoxic than 2BPA, both compounds showed very similar neurotoxicity. PGBE and 2BPA strongly affected the cell cycle, induced oxidative stress and perturbed energy and lipid metabolism. They also targeted specific nervous system processes, such as axon guidance and synapse organization. Finally, 2BPA may trigger ferroptosis by increased iron uptake. Our results show an urgent need for public health authorities to carefully assess the risk glycol ethers pose to humans, to properly protect the workers as well as individuals in the general population unknowingly exposed from indoor air contaminations.

pharmacology and toxicology↗