bioRxiv Science⌕ Search
Home/Archive/bioRxiv

bioRxiv · 10.1101/2023.12.14.571767

Corticopostural functional and effective connectivity reveal cortical control of postural sway velocity during quiet standing

Fauvet, M.·Ziane, C.·Arsenault-Levesque, L.·Fornerone, T.·Dal Maso, F.
View original source ↗Export metadata ↓

Abstract

BackgroundDespite a large body of evidence showing the involvement of the sensorimotor cortex in postural control, its exact role remains unclear. Models of postural control outcomes suggested that the velocity of the center of pressure is a crucial parameter to maintain balance. Inspired by corticokinematic coherence, we hypothesized that cortical oscillations and the velocity of the center of pressure (CoP) would synchronize and that this synchronization would increase with postural task difficulty during quiet standing. MethodsWe compared the magnitude of coherence and Granger causality computed between brain oscillations recorded with electroencephalography and the center of pressure velocity in the Delta and Theta frequency bands obtained from 23 participants performing four quiet standing tasks with various levels of difficulty. The effect of postural task difficulty and information flow direction were tested with a linear mixed model while non-parametric correlations were computed between coherence magnitude and postural performance measured by 95% confidence ellipse area and mean center of pressure velocity. ResultsWe found significant coherence between the Cz EEG electrode and CoP velocity in the Delta and Theta frequency bands. This EEG-CoP velocity coherence significantly increased with task difficulty in the Delta (F = 18.8, p < 0.001) and Theta (F = 7.83, p < 0.001) bands. Granger causality significantly increased with task difficulty (F = 12.5, p < 0.001) and was higher in the efferent than afferent direction (F = 78, p < 0.001). The 95% confidence ellipse area was correlated to coherence magnitude in the most difficult condition. Participants showing significant Granger causality in the afferent direction showed more stable postural outcomes. ConclusionOur results confirm that the CoP velocity has a crucial role in postural control through its synchronization with sensorimotor cortex oscillations. The efferent information predominance suggests that posture is partly controlled by the sensorimotor cortex by a mechanism named corticopostural coherence. Our results show that this corticopostural coherence could represent a mechanism for controlling balance during quiet standing.

Explore related subjects

neurosciencePreprint

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Fauvet, M., Ziane, C., Arsenault-Levesque, L., Fornerone, T., Dal Maso, F.. 2023-12-15. Corticopostural functional and effective connectivity reveal cortical control of postural sway velocity during quiet standing. https://doi.org/10.1101/2023.12.14.571767

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↗