Portrait de Danilo Bzdok

Danilo Bzdok

Membre académique principal
Chaire en IA Canada-CIFAR
Professeur agrégé, McGill University, Département de génie biomédicale
Sujets de recherche
Apprentissage profond
Biologie computationnelle
Grands modèles de langage (LLM)
Traitement du langage naturel

Biographie

Danilo Bzdok est informaticien et médecin de formation. Il possède une double formation unique en neurosciences systémiques et en algorithmes d'apprentissage automatique. Après une formation à l'Université d'Aix-la-Chapelle (RWTH) (Allemagne), à l'Université de Lausanne (Suisse) et à la Harvard Medical School (États-Unis), il a obtenu un doctorat en neurosciences du Centre de recherche de Jülich (Allemagne) et un doctorat en informatique dans le domaine des statistiques d'apprentissage automatique à l'INRIA Saclay et à NeuroSpin (Paris, France). Il est actuellement professeur agrégé à la Faculté de médecine de l'Université McGill et titulaire d’une chaire en IA Canada-CIFAR à Mila – Institut québécois d'intelligence artificielle. Son activité de recherche interdisciplinaire est centrée sur la réduction des lacunes dans la connaissance des bases cérébrales des types de pensée qui définissent l'être humain, afin de découvrir les principes clés de conception computationnelle qui sous-tendent l'intelligence humaine.

Étudiants actuels

Publications

Dissociable influences of maternal vs paternal Alzheimer’s risk on neurocognitive and cardiovascular health in men and women
Frederic St‐Onge
Sylvia Villeneuve
AmanPreet Badhwar
Sarah A Gagliano Taliun
Sali Farhan
Maiya R. Geddes
Yasser Iturria Medina
Judes Poirier
R. Nathan Spreng
We uncovered IPs of AD susceptibility differently expressed in male and female probands and affected by the diagnosed parent’s sex. Matern… (voir plus)al inheritance highlighted memory performance in both sexes, whereas paternal inheritance was particularly linked to cardiovascular health in males. The inheritance of the IPs was reflected in the brain structure at both superficial and deeper layers of the cortex. As the first study of its kind, our cross‐generational analysis of matri‐ vs. patrilinear AD risk bridges the epidemiological and clinical literature by leveraging the power of ∼1,000 patient visits. Our completely data‐driven framework ultimately dissociated phenotypes of maternal and paternal AD risk single‐handedly expressed in male and female probands.
Simulation‐based effect size analysis in the absence of drug effects to inform the design of clinical trials in Alzheimer’s disease
Daniel Andrews
Douglas L Arnold
Simon Ducharme
Howard Chertkow
D Louis Collins
Our results suggest low false positive probabilities for the successful trials. Cohort composition, sampling, and other trial characteristic… (voir plus)s might influence treatment‐independent group difference in cognitive decline rate. With our method, future trials could target treatment effects outside the target population’s false positive range.
General anaesthesia reduces the uniqueness of brain connectivity across individuals and across species
Andrea I. Luppi
Daniel Golkowski
Andreas Ranft
Rudiger Ilg
Denis Jordan
Adrian M. Owen
Lorina Naci
Emmanuel A. Stamatakis
Enrico Amico
Bratislav Misic
The human brain is characterised by idiosyncratic patterns of spontaneous thought, rendering each brain uniquely identifiable from its neura… (voir plus)l activity. However, deep general anaesthesia suppresses subjective experience. Does it also suppress what makes each brain unique? Here we used functional MRI under the effects of the general anaesthetics sevoflurane and propofol to determine whether anaesthetic-induced unconsciousness diminishes the uniqueness of the human brain: both with respect to the brains of other individuals, and the brains of another species. We report that under anaesthesia individual brains become less self-similar and less distinguishable from each other. Loss of distinctiveness is highly organised: it co-localises with the archetypal sensory-association axis, correlating with genetic and morphometric markers of phylogenetic differences between humans and other primates. This effect is more evident at greater anaesthetic depths, reproducible across sevoflurane and propofol, and reversed upon recovery. Providing convergent evidence, we show that under anaesthesia the functional connectivity of the human brain becomes more similar to the macaque brain. Finally, anaesthesia diminishes the match between spontaneous brain activity and meta-analytic brain patterns aggregated from the NeuroSynth engine. Collectively, the present results reveal that anaesthetised human brains are not only less distinguishable from each other, but also less distinguishable from the brains of other primates, with specifically human-expanded regions being the most affected by anaesthesia.
Aberrant functional brain network organization is associated with relapse during 1-year follow-up in alcohol-dependent patients
Justin Böhmer
Pablo Reinhardt
Maria Garbusow
Michael Marxen
Michael N. Smolka
U. Zimmermann
Andreas Heinz
Eva Friedel
Johann Kruschwitz
Henrik Walter
Alcohol dependence (AD) is a debilitating disease associated with high relapse rates even after long periods of abstinence. Thus, elucidatin… (voir plus)g neurobiological substrates of relapse risk is fundamental for the development of novel targeted interventions that could promote long-lasting abstinence. In the present study, we analyzed resting-state functional magnetic resonance imaging (rsfMRI) data from a sample of recently detoxified AD patients (n = 93) who were followed-up for 12 months after rsfMRI assessment. Specifically, we employed graph theoretic analyses to compare functional brain network topology and functional connectivity between future relapsers (REL, n = 59), future abstainers (ABS, n = 28) and age and gender matched controls (CON, n = 83). Our results suggest increased whole-brain network segregation, decreased global network integration and overall blunted connectivity strength in REL compared to CON. Conversely, we found evidence for a comparable network architecture in ABS relative to CON. At the nodal level, REL exhibited decreased integration and decoupling between multiple brain systems compared to CON, encompassing regions associated with higher-order executive functions, sensory and reward processing. Among AD patients, increased coupling between nodes implicated in reward valuation and salience attribution constitutes a particular risk factor for future relapse. Importantly, aberrant network organization in REL was consistently associated with shorter abstinence duration during follow-up, portending to a putative neural signature of relapse risk in AD. Future research should further evaluate the potential diagnostic value of the identified changes in network topology and functional connectivity for relapse prediction at the individual subject level.
Distinctive Whole-brain Cell-Types Predict Tissue Damage Patterns in Thirteen Neurodegenerative Conditions
Veronika Pak
Quadri Adewale
Mahsa Dadar
Yashar Zeighami
Yasser Iturria-Medina
Abstract For over a century, brain research narrative has mainly centered on neuron cells. Accordingly, most whole-brain neu… (voir plus)rodegenerative studies focus on neuronal dysfunction and their selective vulnerability, while we lack comprehensive analyses of other major cell-types’ contribution. By unifying spatial gene expression, structural MRI, and cell deconvolution, here we describe how the human brain distribution of canonical cell-types extensively predicts tissue damage in eleven neurodegenerative disorders, including early- and late-onset Alzheimer’s disease, Parkinson’s disease, dementia with Lewy bodies, amyotrophic lateral sclerosis, frontotemporal dementia, and tauopathies. We reconstructed comprehensive whole-brain reference maps of cellular abundance for six major cell-types and identified characteristic axes of spatial overlapping with atrophy. Our results support the strong mediating role of non-neuronal cells, primarily microglia and astrocytes, on spatial vulnerability to tissue loss in neurodegeneration, with distinct and shared across-disorders pathomechanisms. These observations provide critical insights into the multicellular pathophysiology underlying spatiotemporal advance in neurodegeneration. Notably, they also emphasize the need to exceed the current neuro-centric view of brain diseases, supporting the imperative for cell-specific therapeutic targets in neurodegeneration.
Global fMRI signal topography differs systematically across the lifespan
Jason S. Nomi
Jingwei Li
Taylor Bolt
Catie Chang
Salome Kornfeld
Zachary T. Goodman
B.T. Thomas Yeo
R. Nathan Spreng
Lucina Q. Uddin
The global signal (GS) in resting-state fMRI, known to contain artifacts and non-neuronal physiological signals, also contains important neu… (voir plus)ral information related to individual state and trait characteristics. Here we show distinct linear and curvilinear lifespan patterns of GS topography in a cross-sectional lifespan sample, demonstrating its importance for consideration in studies of development and aging. Subcortical brain regions such as the thalamus and putamen show linear associations with the GS across the lifespan. The thalamus has stronger coupling in older-age individuals compared with younger-aged individuals, while the putamen has stronger coupling in younger individuals compared with older individuals. The subcortical nucleus basalis shows a u-shaped pattern similar to cortical regions within the lateral frontoparietal network and dorsal attention network, where coupling with the GS is stronger at early and old age, with weaker coupling in middle age. This differentiation in coupling strength between subcortical and cortical brain activity across the lifespan supports a dual-layer model of GS composition, where subcortical aspects of the GS are differentiated from cortical aspects of the GS. We find that these subcortical-cortical contributions to the GS depend strongly on the lifespan stage of individuals. Our findings demonstrate how neurobiological information within the GS differs across development and highlight the need to carefully consider whether or not to remove this signal when investigating age-related functional differences in the brain.
Multivariate analytical approaches for investigating brain-behavior relationships
E. Leighton Durham
Andrew J. Stier
Carlos Cardenas-Iniguez
Gabrielle E. Reimann
Hee Jung Jeong
Randolph M. Dupont
Xiaoyu Dong
Tyler M. Moore
Marc G. Berman
Benjamin B. Lahey
Antonia N. Kaczkurkin
The default network dominates neural responses to evolving movie stories
Filip Milisav
Avram J. Holmes
Georgios D. Mitsis
Bratislav Misic
Emily S. Finn
Neuroscientific studies exploring real-world dynamic perception often overlook the influence of continuous changes in narrative content. In … (voir plus)our research, we utilize machine learning tools for natural language processing to examine the relationship between movie narratives and neural responses. By analyzing over 50,000 brain images of participants watching Forrest Gump from the studyforrest dataset, we find distinct brain states that capture unique semantic aspects of the unfolding story. The default network, associated with semantic information integration, is the most engaged during movie watching. Furthermore, we identify two mechanisms that underlie how the default network liaises with the amygdala and hippocampus. Our findings demonstrate effective approaches to understanding neural processes in everyday situations and their relation to conscious awareness.
Genesis, modelling and methodological remedies to autism heterogeneity
Juliette Rabot
Eya‐mist Rødgaard
Ridha Joober
Boris C Bernhardt
Sébastien Jacquemont
Laurent Mottron
156. Modeling Eye Gaze to Videos Using Dynamic Trajectory Variability Analysis
Qianying Wu
Na Yeon Kim
Jasmin Turner
Umit Keles
Lynn Paul
Ralph Adolphs
Bayesian stroke modeling details sex biases in the white matter substrates of aphasia
Julius M. Kernbach
Gesa Hartwigsen
Jae-Sung Lim
Hee-Joon Bae
Kyung-Ho Yu
Gottfried Schlaug
Anna Bonkhoff
Natalia S. Rost
Ischemic cerebrovascular events often lead to aphasia. Previous work provided hints that such strokes may affect women and men in distinct w… (voir plus)ays. Women tend to suffer strokes with more disabling language impairment, even if the lesion size is comparable to men. In 1401 patients, we isolate data-led representations of anatomical lesion patterns and hand-tailor a Bayesian analytical solution to carefully model the degree of sex divergence in predicting language outcomes ~3 months after stroke. We locate lesion-outcome effects in the left-dominant language network that highlight the ventral pathway as a core lesion focus across different tests of language performance. We provide detailed evidence for sex-specific brain-behavior associations in the domain-general networks associated with cortico-subcortical pathways, with unique contributions of the fornix in women and cingular fiber bundles in men. Our collective findings suggest diverging white matter substrates in how stroke causes language deficits in women and men. Clinically acknowledging such sex disparities has the potential to improve personalized treatment for stroke patients worldwide.
Fasting alters the gut microbiome reducing blood pressure and body weight in metabolic syndrome patients
András Maifeld
Hendrik Bartolomaeus
Ulrike Löber
Ellen G. Avery
Nico Steckhan
Lajos Markó
Nicola Wilck
Ibrahim Hamad
Urša Šušnjar
Anja Mähler
Christoph Hohmann
Chia-Yu Chen
Holger Cramer
Gustav Dobos
Till Robin Lesker
Till Strowig
Ralf Dechend
Markus Kleinewietfeld
Andreas Michalsen … (voir 2 de plus)
Dominik N. Müller
Sofia K. Forslund
Abstract Periods of fasting and refeeding may reduce cardiometabolic risk elevated by Western diet. We show that in hypertensive metabolic s… (voir plus)yndrome (MetS) patients (n=35), a 5-day fast followed by a modified DASH diet (Dietary Approach to Stop Hypertension) reduced systolic blood pressure (SBP), antihypertensive medication need, and body-mass index (BMI) at three months post intervention compared to a modified DASH diet alone (n=36). Fasting altered the gut microbiome, impacting bacterial taxa and gene modules associated with short-chain fatty acid production. Cross-system analyses revealed a positive correlation of circulating mucosa-associated invariant T (MAIT) cells, non-classical monocytes and CD4+ effector T cells with SBP. Furthermore, regulatory T cells (Tregs) positively correlated with BMI and weight. Machine learning could predict sustained SBP-responsiveness within the fasting group from baseline immunome data, identifying CD8+ effector T cells, Th17 cells and Tregs as important contributors to the model. The high-resolution multi-omics data highlights fasting as a promising non-pharmacological intervention in MetS.