Publications by authors named "Alessandra Bertoldo"

Functional magnetic resonance imaging (fMRI) studies in cognitive and clinical neuroscience rely on blood oxygenation level-dependent (BOLD) contrast, measured with single-shot gradient-echo-planar imaging. However, conventional schemes encompass the acquisition of single-echo fMRI, which samples a single echo at a single-echo time (TE), facing limitations in disentangling neural signals from artifacts. Multi-echo (ME) fMRI captures images at multiple echo times within a single repetition time (TR) period and enables the separation of BOLD and non-BOLD signal components.

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Positron emission tomography (PET) and single photon emission computed tomography (SPECT) are essential molecular imaging tools for the in vivo investigation of neurotransmission. Traditionally, PET and SPECT images are analysed in a univariate manner, testing for changes in radiotracer binding in regions or voxels of interest independently of each other. Over the past decade, there has been an increasing interest in the so-calledapproach that captures relationships of molecular imaging measures in different brain regions.

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Intrinsic brain activity is characterized by pervasive long-range temporal correlations. While these scale-invariant dynamics are a fundamental hallmark of brain function, their implications for individual-level metabolic regulation remain poorly understood. Here, we address this gap by integrating resting-state functional Magnetic Resonance Imaging (fMRI) and dynamic [F]FDG Positron Emission Tomography (PET) data acquired from the same cohort of participants.

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Deep learning is significantly advancing the analysis of electroencephalography (EEG) data by effectively discovering highly nonlinear patterns within the signals. Data partitioning and cross-validation are crucial for assessing model performance and ensuring study comparability, as they can produce varied results and data leakage due to specific signal properties (e.g.

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Introduction: Despite accounting for only 2% of body weight, the human brain requires significant amounts of glucose, even at rest, underscoring the importance of functional-metabolic relationships. Previous studies revealed moderate associations between resting-state fMRI functional connectivity (FC) and local metabolism via [F]FDG-PET, yet much remains to be understood, particularly regarding their coupling between functional and metabolic networks.

Methods: To this end, we employed multivariate Partial Least Squares Correlation (PLSC) to investigate the functional-metabolic relationship at both nodal and network level.

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Gliomas alter brain function and integrity, but these disruptions are often studied separately. This study utilised a novel approach that integrated functional, structural and microstructural connectivity information to investigate glioma-induced brain network changes and their clinical implications. It focused on the impact of gliomas on key brain networks, with a particular emphasis on the relationship between tumour topology and its effect on homotopic areal-level parcellation.

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Positron emission tomography (PET)-based connectivity analysis provides a molecular perspective that complements fMRI-derived functional connectivity. However, lack of standardized terminology and diverse methodologies in PET connectivity studies has resulted in inconsistencies, complicating the interpretation and comparison of results across studies. A standardized nomenclature is thus needed to reduce ambiguity, enhance reproducibility, and facilitate interpretability across radiotracers, imaging modalities and studies.

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The brain's resting-state energy consumption is expected to be driven by spontaneous activity. We previously used 50 resting-state fMRI (rs-fMRI) features to predict [F]FDG SUVR as a proxy of glucose metabolism. Here, we expanded on our effort by estimating [F]FDG kinetic parameters (irreversible uptake), (delivery), (phosphorylation) in a large healthy control group (n = 47).

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Brain Tumor Segmentation (BraTS) challenges have significantly advanced research in brain tumor segmentation and related medical imaging tasks. This paper provides a comprehensive review of the BraTS datasets from 2012 to 2024, examining their evolution, challenges, and contributions to MRI-based brain tumor segmentation. Over the years, the datasets have grown in size, complexity, and scope, incorporating refined pre-processing and annotation protocols.

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Background: Fatigue in Parkinson's disease (PD) is a prevalent and debilitating non-motor symptom. Despite its significant impact on quality of life, the underlying neurochemical and network-based mechanisms remain poorly understood.

Objectives: This observational study applied a multimodal imaging approach to explore potential links between the functional connectivity of neurotransmitter-specific circuits and fatigue in a sample of patients with PD.

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Objectives: The present study aims to investigate the role that cognitive cerebellar lobules, compared to the motor ones, could have on performance abilities control in older individuals with Mild Cognitive Impairment (MCI).

Methods: Thirty-six participants with MCI were retrospectively recruited from the outpatient clinic for Cognitive Decline and Dementia at Geriatric Clinic and Regional Center for Brain Aging. Cognition was assessed through a reaction time (RT) task in which a mere cognitive (COG) component (RT/S1 COG, RT/S3 COG) has been isolated from a motor (MOT) component (RT/S1 MOT, RT/S3 MOT).

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The last decade has witnessed a notable surge in deep learning applications for electroencephalography (EEG) data analysis, showing promising improvements over conventional statistical techniques. However, deep learning models can underperform if trained with bad processed data. Preprocessing is crucial for EEG data analysis, yet there is no consensus on the optimal strategies in deep learning scenarios, leading to uncertainty about the extent of preprocessing required for optimal results.

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Purpose: PET imaging is a pivotal tool for biomarker research aimed at personalized medicine. Leveraging the quantitative nature of PET requires knowledge of plasma radiotracer concentration. Typically, the arterial input function (AIF) is obtained through arterial cannulation, an invasive and technically demanding procedure.

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Article Synopsis
  • * Various shape analysis methods, including scalar curvature signatures and advanced computational techniques, were used to evaluate the cortical structures, aiming to enhance predictions of fetal gestational age.
  • * The GSHOT method proved to be the most effective in predicting gestational age, with higher accuracy in neurotypical fetuses compared to pathological ones, thereby offering a sophisticated tool for studying fetal brain development.
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Transient or persistent hypo-anosmia is common in SARS‑CoV‑2 infection but olfactory pathway late-term morphometric changes are still under investigation. We evaluated late olfactory bulb (OB) imaging changes and their correlates with the olfactory function in otherwise neurologically asymptomatic COVID-19 patients. Eighty-three subjects (mean-age 43 ± 14 yr; 54 females; time-interval infection/MRI: 129±68 d) were affected by asymptomatic to mild COVID-19 in 2020 and 25 healthy controls (mean-age 40 ± 13 yr; 9 females) underwent 3T-MRI and olfactory function evaluation through anamnestic questionnaire and Sniffin' Sticks.

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The relationship between the brain's structural wiring and its dynamic activity is thought to vary regionally, implying that the mechanisms underlying structure-function coupling may differ depending on a region's position within the brain's hierarchy. To better bridge the gap between structure and function, it is crucial to identify the factors shaping this regionality, not only in terms of how static functional connectivity aligns with structure, but also regarding the time-domain variability of this interplay. Here we map structure - function coupling and its time-domain variability and relate them to the heterogeneity of the cortex.

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Purpose: This study evaluates the potential of within-individual Metabolic Connectivity (wi-MC), from dynamic [F]FDG PET data, based on the Euclidean Similarity method. This approach leverages the biological information of the tracer's full temporal dynamics, enabling the direct extraction of individual metabolic connectomes. Specifically, the proposed framework, applied to glioma pathology, seeks to assess sensitivity to metabolic dysfunctions in the whole brain, while simultaneously providing further insights into the pathophysiological mechanisms regulating glioma progression.

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Age-related changes in the BOLD response could reflect neurovascular coupling modifications rather than simply impairments in neural functioning. In this study, we propose the use of a sparse dynamic causal model (sDCM) to decouple neuronal and vascular factors in the BOLD signal, with the aim of characterizing the whole-brain spatial pattern of hemodynamic sensitivity to healthy aging, as well as to test the role of hemodynamic features as independent predictors in an age-classification model. sDCM was applied to the resting-state functional magnetic resonance imaging data of a cohort of 126 healthy individuals in a wide age range (31 females), providing reliable estimates of the hemodynamic response function (HRF) for each subject and each region of interest.

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The brain's resting-state energy consumption is expected to be mainly driven by spontaneous activity. In our previous work, we extracted a wide range of features from resting-state fMRI (rs-fMRI), and used them to predict [F]FDG PET SUVR as a proxy of glucose metabolism. Here, we expanded upon our previous effort by estimating [F]FDG kinetic parameters according to Sokoloff's model, i.

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This study challenges the traditional focus on zero-lag statistics in resting-state functional magnetic resonance imaging (rsfMRI) research. Instead, it advocates for considering time-lag interactions to unveil the directionality and asymmetries of the brain hierarchy. Effective connectivity (EC), the state matrix in dynamical causal modeling (DCM), is a commonly used metric for studying dynamical properties and causal interactions within a linear state-space system description.

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Background: In multiple sclerosis (MS), imaging biomarkers play a crucial role in characterizing the disease at the time of diagnosis. MRI and optical coherence tomography (OCT) provide readily available biomarkers that may help to define the patient's clinical profile. However, the evaluation of cortical and paramagnetic rim lesions (CL, PRL), as well as retinal atrophy, is not routinely performed in clinic.

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Introduction: Recent evidence suggests the blood-to-brain influx rate ( ) in imaging as a promising biomarker of blood-brain barrier () permeability alterations commonly associated with peripheral inflammation and heightened immune activity in the brain. However, standard compartmental modeling quantification is limited by the requirement of invasive and laborious procedures for extracting an arterial blood input function. In this study, we validate a simplified blood-free methodologic framework for estimation by fitting the early phase tracer dynamics using a single irreversible compartment model and an image-derived input function ().

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In high-grade gliomas, pseudoprogression after radiation treatment might dramatically impact patient's management. We searched for perioperative imaging predictors of pseudoprogression in high-grade gliomas according to PRISMA guidelines, using MEDLINE/Pubmed and Embase (until January 2024). Study design, sample size, setting, diagnostic gold standard, imaging modalities and contrasts, and differences among variables or measures of diagnostic accuracy were recorded.

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Despite substantial advances in cancer treatment, for patients with glioblastoma prognosis remains bleak. The emerging field of cancer neuroscience reveals intricate functional interplays between glioblastoma and the cellular architecture of the brain, encompassing neurons, glia, and vessels. New findings underscore the role of structural and functional connections within hierarchical networks, known as the connectome.

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The present study aims to investigate the relationship between cerebellar volumes and cognitive reserve in individuals with Mild Cognitive Impairment (MCI). A description of proxies of cerebellar cognitive reserve in terms of different volumes across lobules is also provided. 36 individuals with MCI underwent neuropsychological (MoCA, MMSE, Clock test, CRIq) assessment and neuroimaging acquisition with magnetic resonance imaging at 3 T.

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