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Author

M. Bergamino

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Jul 2026

Assessing mTBI-related brain changes: insights from bi-exponential and tri-exponential intravoxel incoherent motion (IVIM) MRI models.

This pilot study investigated microstructural and perfusion changes in individuals with mTBI using both bi-exponential and tri-exponential intravoxel incoherent motion (IVIM) MRI models. Twenty patients with mTBI in the subacute phase and 20 healthy controls (HCs) underwent advanced diffusion MRI, with a subset of 11 controls participating in a test-retest reliability analysis. The tri-exponential IVIM model, which separates diffusion and perfusion into three distinct compartments, demonstrated superior sensitivity and reproducibility compared to the conventional bi-exponential model. Voxel-wise analysis revealed that mTBI subjects showed widespread alterations in IVIM parameters, including reduced apparent slow diffusion (Ds) and elevated perfusion-related fractions (Fp and Ff), particularly in frontal white matter, corpus callosum, and subcortical regions. These changes were robustly associated with lower cognitive performance, as measured by the Montreal Cognitive Assessment (MoCA), highlighting the link between microstructural integrity, perfusion, and cognitive outcomes. While IVIM parameters showed strong correlations with MoCA scores, their associations with the Glasgow Outcome Scale-Extended (GOS-E) were more modest, reflecting the complexity of brain injury recovery. This study represents the first direct comparison of bi-exponential and tri-exponential IVIM models in the context of mTBI, demonstrating their capacity to detect subtle brain alterations that remain undetected by conventional imaging and standard diffusion models. Additionally, these findings indicate that the tri-exponential IVIM approach might be a promising and reliable tool for non-invasively characterizing brain changes following mTBI, suggesting its potential utility as an imaging biomarker in brain injury research.

M. Bergamino, L. R. Ott, M. M. McElvogue et al. · 0 citations
Open access Jul 2026

Distinct nigral and brainstem pathology markers map onto separable subthalamic electrophysiological signatures in Parkinson’s disease

Subthalamic local field potentials (LFPs) are increasingly used as physiomarkers of the symptomatic state in Parkinson’s disease, but their relationship to the underlying neurodegenerative pathology remains unclear. Here, we combined OFF-medication subthalamic LFP recordings with quantitative MRI markers of nigral and brainstem pathology in 33 people with Parkinson’s disease. Distinct pathological markers mapped onto dissociable electrophysiological components. Substantia nigra pars compacta susceptibility was associated with increased occupancy, duration and rate of low-β bursts, whereas nigral free water was associated with greater low-frequency aperiodic offset and a steeper slope. Pedunculopontine nucleus free-water- corrected axial diffusivity was selectively associated with high-frequency aperiodic activity, and this relationship strengthened with increasing nigral susceptibility, consistent with dopaminergic-state- dependent influences of extranigral pathology on subthalamic physiology. Only low-frequency aperiodic offset was also associated with contralateral bradykinesia. These findings indicate that the subthalamic LFP is not a unitary readout of dopamine loss or motor state, but an integrated physiological signal in which pathology across interconnected systems is expressed through separable oscillatory and aperiodic components. Chronically implanted devices may therefore provide physiological readouts of underlying disease biology alongside control signals for adaptive therapy.

A. Delgado-Sanchez, L. Andrews, P. Hayton et al. · 0 citations

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