bioRxiv Science⌕ Search

Biology subjects

Uccella, S.

Publications and source records attributed to Uccella, S..

2 recordsLinked to original sources

Vessel Spatial Analysis (VeSpA): a tool for whole slide image segmentation, morphometry, and QuPath extension.

Quantifying vascular architecture in histological whole slide images is needed to study tissue organisation, tumour microenvironment biology, and diseaseassociated vascular remodelling. However, vessel analysis in routine immunohistochemistry remains challenging. Available workflows are often manual, require programming expertise, or lack direct integration with digital pathology platforms. We developed VeSpA (Vessel Spatial Analysis), an open-source pipeline and QuPath extension for automated vessel segmentation and morphometric quantification in CD31-stained whole slide images. VeSpA combines configurable signal extraction, using CMYK Yellow channel extraction by default and optional DAB stain deconvolution for H-DAB images, with automatic or percentile-based thresholding, morphological refinement, contour filtering, and lumen filling to generate vessel masks from standard DAB-stained sections. The QuPath extension includes a graphical interface for selecting annotations, TMA cores, or whole images, configuring segmentation parameters, running the Python backend, and importing vessel objects directly into the QuPath hierarchy. For each detected vessel, VeSpA extracts area, major axis length, minor axis length, eccentricity, centroid, and orientation, while also appending summary measurements to parent annotations and TMA cores. Validation against independent pathologist annotations showed that VeSpA achieved segmentation performance close to inter-rater agreement and outperformed yellow channel prompt-based SAM and zero-shot YOLOv8-seg on overlap-based metrics in the tested dataset. VeSpA integrates vessel segmentation, morphometric feature extraction, and QuPath-based visualisation into a single reproducible workflow for vascular quantification in computational pathology and spatial analysis of histological tissue architecture.

pathology↗

Quantifying cortical maturational aspects during different vigilance states in preterm infants by advanced EEG analysis

Preterm birth is associated with numerous neurodevelopmental adverse outcomes, even in the absence of acquired lesions, as it occurs during a critical period of brain development. Clear organization of vigilance states can be recognized from 30-32 weeks postmenstrual age (PMA). In this study, we investigated whether spatial and temporal properties of neuronal oscillatory dynamics (i.e., phase synchronization, bistability, and cross-frequency coupling) during different vigilance states provide insights into cortical maturation in preterm infants born very low birth weight (VLBW) at low neurological risk and devoid of detectable brain lesions. We analyzed artifact-free video-polysomnographic data from 11 VLBW preterm infants (PMA at recording: 33.0 {+/-} 1.6 weeks) who underwent brain MRI at term-equivalent age. For each vigilance state, we computed the weighted Phase Lag Index (wPLI), Bistability Index (BiS), and Phase-Amplitude Coupling (PAC), both globally and across anterior and posterior regions, and examined their correlation with PMA at recording. wPLI, BiS, and PAC showed specific trends across vigilance states. BiS and PAC exhibited posterior-to-anterior differences and correlated with PMA. Our study suggests that these electrophysiological markers, particularly BiS and PAC, may serve as indices to monitor aspects of cortical maturation in VLBW at low neurological risk.

neuroscience↗