Search bioRxiv⌕ Search
Home/Archive/bioRxiv

bioRxiv · 10.1101/2025.10.08.680888

Across-speaker articulatory reconstruction from sensorimotor cortex for generalizable brain-computer interfaces

Wu, R.·Berezutskaya, J.·Freudenburg, Z. V.·Ramsey, N. F.
View original source ↗Export metadata ↓

Abstract

ObjectiveSpeech brain-computer interfaces (BCIs) can restore speech features like articulatory movements from brain activity. However, for individuals with vocal tract paralysis, lack of articulatory movements can pose a challenge for speech BCI development. To address this challenge, our study aims at extracting generalizable articulatory features from a group of native Dutch speakers and reconstructing these features from brain data of a separate group of able-bodied individuals. ApproachWe applied a tensor component analysis (TCA) model to extract generalisable articulatory features from a publicly available articulatory movement dataset. To reconstruct articulatory features from the brain, we analyzed data of three able-bodied participants P1, P2 and P3 with high-density electrocorticography (HD-ECoG) electrode arrays implanted over the sensorimotor cortex. For each participant, a separate TCA model was applied to extract neural features. A gradient boosting regression model was used to reconstruct articulatory features from neural features. Reconstruction performance was measured as Pearsons correlation coefficient (PCC) between the reconstructed and the generalizable articulatory features. ResultsThe extracted articulatory features showed even contributions across participants, indicating that these features captured generalizable articulatory kinematic patterns. By using these features, we were able to reconstruct articulatory features from brain data. PCC between the reconstructed and original articulatory features were significantly above chance for all three participants, with mean PCCs of 0.80, 0.75 and 0.76 for P1, P2 and P3 respectively. SignificanceWith the rapid development of speech BCI, our research demonstrates that speech-related articulatory features can be restored from HD-ECoG signal using generalizable articulatory features derived from able-bodied individuals. With the potential to reconstruct audio or speech-related facial movements from the reconstructed articulatory features, our framework may provide a new way for developing speech BCIs for people unable to produce mouth movements.

Source connections

Explore related subjects

neurosciencePreprint

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Wu, R., Berezutskaya, J., Freudenburg, Z. V., Ramsey, N. F.. 2025-10-08. Across-speaker articulatory reconstruction from sensorimotor cortex for generalizable brain-computer interfaces. https://doi.org/10.1101/2025.10.08.680888

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

bioRxiv2026

The Unreasonable Effectiveness of Cell Types in Describing Neuronal Physiological Features

Single-cell RNA sequencing (scRNA-seq) captures detailed gene expression profiles at scale, while patch-clamp recordings measure intrinsic neuronal electrophysiological properties. Modeling the relations between these two modalities remains a challenge. Here, we compare how well electrophysiological features can be predicted by traditional transcriptomic cell type classification, representations derived from a foundational model (scGPT) pretrained on large-scale scRNA-seq datasets, ion channel-coding genes, and highly variable genes. Using paired transcriptomic and electrophysiological patch-sequencing data from 495 human neurons from neurosurgical tissue, we find that cluster-level cell type representations consistently outperform highly variable gene selection, ion channel gene selection, and context-enriched scGPT embeddings. Notably, performance varies across model architectures and initializations, and the best results are obtained by combining the outputs of separate cell type and scGPT-based models. Together, these findings suggest that traditional discrete cellular classification is highly effective in predicting physiological features. For maximum performance it can be complemented by pretrained transformer models.

neuroscience↗
bioRxiv2026

A nonlinear inhibition pathway underlying cortical responses to tuned holographic optogenetic perturbations

Optogenetics enables causal manipulation of cortical activity. Perturbation responses can be counterintuitive due to network interactions, making theory essential for predicting them. Existing approaches often rely on linear approximations, which fail for many biologically relevant perturbations. Here we develop a nonlinear theory of responses to holographic perturbations in cell-type-specific recurrent networks with structured connectivity. We fit a nonlinear model to mouse V1 data, which shows cotuned-ensemble suppression: perturbing spatially clustered neurons with similar preferred orientations yields markedly stronger short-range suppression than perturbing untuned ensembles. We show that cotuned-ensemble suppression arises from a feature-tuned, nonlinear inhibition pathway implicating somatostatin-positive (SST) interneurons. The theory predicts that cotuned ensembles suppress parvalbumin-positive (PV) neurons but facilitate SST neurons, and links the degree of cotuned-ensemble suppression or facilitation to the variance of the SST response. This framework identifies mechanisms by which nonlinear inhibition sculpts cortical dynamics and establishes a predictive basis for targeted optogenetic interventions.

neuroscience↗
bioRxiv2026

Proteomic signatures of APOE ε4 across human tissues and cell types in Alzheimers disease

The apolipoprotein E {varepsilon}4 (APOE {varepsilon}4) allele is the strongest genetic risk factor for late-onset Alzheimers disease (AD). However, the underlying molecular mechanisms remain unclear. This study included 1691 participants from the Religious Orders Study and Rush Memory and Aging Project (ROSMAP), 1226 participants from the Accelerating Medicines Partnership - Alzheimers Disease (AMP-AD) Diverse Cohorts Study, and 735 participants from the Alzheimers Disease Neuroimaging Initiative (ADNI). To characterise APOE {varepsilon}4 molecular effects, we analysed proteomic data from plasma, cerebrospinal fluid (CSF), and induced pluripotent stem cell (iPSC)-derived astrocytes and neurons, as well as transcriptomic and proteomic data from multiple brain regions. The association of APOE {varepsilon}4 with AD neuropathology was also examined. APOE {varepsilon}4 carriers shared a plasma proteomic signature enriched for immune processes, irrespective of AD diagnosis. A machine learning classifier trained on this signature discriminated APOE {varepsilon}4 carriers from non-carriers in an independent cohort using CSF proteomics. APOE {varepsilon}4 carriage was associated with higher Braak stages and Consortium to Establish a Registry for Alzheimers Disease (CERAD) score. However, only limited APOE {varepsilon}4-associated transcriptomic and proteomic changes were observed in bulk brain tissue, with poor cross-layer concordance. Proteomic analyses of iPSC-derived astrocytes and neurons further revealed cell-type-specific APOE {varepsilon}4-associated changes. APOE {varepsilon}4 is associated with a consistent proteomic signature across plasma and CSF. Its molecular effects in the brain differ across cell types, brain regions and molecular layers. These findings support the need for cell-type-resolved multi-omic studies to elucidate how APOE {varepsilon}4 confers AD risk.

neuroscience↗