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Sacchi, L.

Publications and source records attributed to Sacchi, L..

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Benchmarking Clustering Strategies for High-Dimensional Spike Time-Windows Data from Multi-Electrode Arrays

From a statistical point of view, clustering spike time-windows from multi-electrode arrays (MEAs) recordings is a challenging high-dimensional, unsupervised clustering task where stationarity, commonly assumed in standard time-series analysis, is often violated and for which a gold standard is currently unavailable. Here we aim at providing practical guidance on how to cluster this type of data by systematically comparing 108 clustering pipelines differing along three main dimensions: (i) the data feature space; (ii) the metrics used to quantify distance between data points; and (iii) the clustering algorithm. For our benchmark we used both labeled synthetic data, mimicking four physiologically-inspired classes of spike time-windows, and a set of real MEAs recordings from a two-dimensional in-vitro neural culture. The performance of the competing pipelines was evaluated in terms of balanced accuracy and computational time when analyzing the synthetic datasets, while the Silhouette score was used for the real dataset, where no ground-truth is available. Overall, our analysis shows that the best combination is formed by k-means with Euclidean distance applied after Principal Component Analysis (PCA) of the spike time-windows. Conversely, hierarchical clustering showed the highest computational burden, while Independent Component Analysis and kernel PCA provided less effective noise suppression.

neuroscience↗

DTI-ALPS PRIMARILY REFLECTS WHITE MATTER DIFFUSION DISPERSION AND MICROSTRUCTURAL HETEROGENEITY IN NEURODEGENERATION: INSIGHTS FROM MULTI-MODAL MRI

1.1.1 BackgroundThe glymphatic system facilitates clearance of metabolic waste and pathological proteins from the brain, and its dysfunction has been implicated in neurodegenerative disease. The diffusion tensor imaging-analysis along the perivascular space (DTI-ALPS) has been proposed as a non-invasive MRI marker of glymphatic flow, although its biological specificity remains uncertain. This study aimed to identify the determinants of DTI-ALPS and evaluate whether it primarily reflects white-matter (WM) microstructure rather than glymphatic flow in the context of neurodegeneration. 1.2 MethodsWe examined 100 individuals referred to the Memory Clinic of the Policlinico Hospital in Milan for suspected dementia. All participants underwent a 3T-MRI protocol including 3D-T1-weighted and 3D-FLAIR imaging, double-shell diffusion-weighted imaging (b=1000/2000 s/mm{superscript 2}), and multi-echo gradient-echo sequences for quantitative susceptibility mapping. Within standard DTI-ALPS ROIs, we extracted DTI-ALPS values together with fractional anisotropy (FA), mean diffusivity (MD), and mode of anisotropy (MA) at both b-values, as well as neurite orientation and density imaging (NODDI) metrics, particularly the orientation dispersion index (ODI). WM microstructure was further characterized using the T1/FLAIR ratio and diamagnetic component of susceptibility (DCS). 1.3 Results and conclusionsDTI-ALPS correlated inversely with MA (r = -0.84 at b = 1000; r = -0.86 at b = 2000) and positively with ODI (r = 0.73). Moderate correlations with the T1/FLAIR ratio and DCS supported sensitivity to WM alterations. Factor analysis indicated that DTI-ALPS clustered with MA and ODI rather than forming a distinct factor, suggesting that DTI-ALPS primarily reflects WM diffusion dispersion and heterogeneity rather than glymphatic flow in the context of neurodegeneration. KeypointsO_LIDTI-ALPS links strongly with mode of anisotropy at high b-values and orientation dispersion, indicating crossing-fibers loss C_LIO_LIDTI-ALPS is moderately associated to T1/FLAIR ratio and diamagnetic susceptibility values, reflecting microstructural WM changes C_LIO_LIDTI-ALPS reflects primarily WM features and may lack specificity for glymphatic flow in the context of neurodegeneration. C_LI

neuroscience↗