arXiv subjects

Giorgio Dolci

Publications and source records attributed to Giorgio Dolci.

4 recordsLinked to original sources

arXiv2026

Algebraic Connectivity Reveals Modulated High-Order Functional Networks in Alzheimer's Disease

Functional MRI is a neuroimaging technique that analyzes the functional activity of the brain by measuring blood-oxygen-level-dependent signals throughout the brain. The derived functional features can be used for investigating brain alterations in neurological and psychiatric disorders. In this work, we employed a hypergraph to model high-order functional relations across brain regions, introducing algebraic connectivity (a(G)) for estimating the hyperedge weights. The hypergraph structure was derived from healthy controls to build a common topology across individuals. The considered cohort for subsequent analyses included subjects covering the Alzheimer's disease (AD) continuum, encompassing both mild cognitive impairment and AD patients. Statistical analysis and three classification tasks: HC vs AD, MCI vs AD, and HC vs MCI, were performed to assess differences across the three groups and the potential of the hyperedge weights as functional features. Furthermore, a mediation analysis was performed to evaluate the reliability of the a(G) values, representing functional information as the mediator between tau-PET levels, a key biomarker of AD, and cognitive scores. The proposed approach identified a larger number of hyperedges statistically different across groups compared to state-of-the-art methods. The a(G) hyperedge weights also demonstrated a higher discriminative power in all three binary classifications. Finally, two hyperedges belonging to salience/ventral attention and somatomotor networks showed a partial mediation effect between the tau biomarker and cognitive decline. These results suggested that a(G) can be an effective approach for extracting the hyperedge weights, including important functional information that resides in the brain areas forming the hyperedges.

q-bio.NC↗

arXiv2025

Guidelines For The Choice Of The Baseline in XAI Attribution Methods

Given the broad adoption of artificial intelligence, it is essential to provide evidence that AI models are reliable, trustable, and fair. To this end, the emerging field of eXplainable AI develops techniques to probe such requirements, counterbalancing the hype pushing the pervasiveness of this technology. Among the many facets of this issue, this paper focuses on baseline attribution methods, aiming at deriving a feature attribution map at the network input relying on a "neutral" stimulus usually called "baseline". The choice of the baseline is crucial as it determines the explanation of the network behavior. In this framework, this paper has the twofold goal of shedding light on the implications of the choice of the baseline and providing a simple yet effective method for identifying the best baseline for the task. To achieve this, we propose a decision boundary sampling method, since the baseline, by definition, lies on the decision boundary, which naturally becomes the search domain. Experiments are performed on synthetic examples and validated relying on state-of-the-art methods. Despite being limited to the experimental scope, this contribution is relevant as it offers clear guidelines and a simple proxy for baseline selection, reducing ambiguity and enhancing deep models' reliability and trust.

cs.AI↗

arXiv2025

An interpretable generative multimodal neuroimaging-genomics framework for decoding Alzheimer's disease

\textbf{Objective:} Alzheimer's disease (AD) is the most prevalent form of dementia worldwide, encompassing a prodromal stage known as Mild Cognitive Impairment (MCI), where patients may either progress to AD or remain stable. The objective of the work was to capture structural and functional modulations of brain structure and function relying on multimodal MRI data and Single Nucleotide Polymorphisms, also in case of missing views, with the twofold goal of classifying AD patients versus healthy controls and detecting MCI converters. % in two distinct tasks, dealing with also missing data.\\ \textbf{Approach:} We propose a multimodal DL-based classification framework where a generative module employing Cycle Generative Adversarial Networks was introduced in the latent space for imputing missing data (a common issue of multimodal approaches). Explainable AI method was then used to extract input features' relevance allowing for post-hoc validation and enhancing the interpretability of the learned representations. \textbf{Main results:} Experimental results on two tasks, AD detection and MCI conversion, showed that our framework reached competitive performance in the state-of-the-art with an accuracy of $0.926\pm0.02$ and $0.711\pm0.01$ in the two tasks, respectively. The interpretability analysis revealed gray matter modulations in cortical and subcortical brain areas typically associated with AD. Moreover, impairments in sensory-motor and visual resting state networks along the disease continuum, as well as genetic mutations defining biological processes linked to endocytosis, amyloid-beta, and cholesterol, were identified. \textbf{Significance:} Our integrative and interpretable DL approach shows promising performance for AD detection and MCI prediction while shedding light on important biological insights.

q-bio.QM↗

arXiv2024

Multimodal MRI Accurately Identifies Amyloid Status in Unbalanced Cohorts in Alzheimer's Disease Continuum

Amyloid-$β$ (A$β$) plaques in conjunction with hyperphosphorylated tau proteins in the form of neurofibrillary tangles are the two neuropathological hallmarks of Alzheimer's disease. It is well-known that the identification of individuals with A$β$ positivity could enable early diagnosis. In this work, we aim at capturing the A$β$ positivity status in an unbalanced cohort enclosing subjects at different disease stages, exploiting the underlying structural and connectivity disease-induced modulations as revealed by structural, functional, and diffusion MRI. Of note, due to the unbalanced cohort, the outcomes may be guided by those factors rather than amyloid accumulation. The partial views provided by each modality are integrated in the model allowing to take full advantage of their complementarity in encoding the effects of the A$β$ accumulation, leading to an accuracy of $0.762\pm0.04$. The specificity of the information brought by each modality is assessed by \textit{post-hoc} explainability analysis (guided backpropagation), highlighting the underlying structural and functional changes. Noteworthy, well-established biomarker key regions related to A$β$ deposition could be identified by all modalities, including the hippocampus, thalamus, precuneus, and cingulate gyrus, witnessing in favor of the reliability of the method as well as its potential in shading light on modality-specific possibly unknown A$β$ deposition signatures.

cs.AI↗