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Section: Partnerships and Cooperations

International Initiatives

Inria Associate Teams Not Involved in an Inria International Labs

LargeBrainNets
  • Title: Characterizing Large-scale Brain Networks Using Novel Computational Methods for dMRI and fMRI-based Connectivity

  • International Partner (Institution - Laboratory - Researcher):

    • Stanford (United States) - Stanford Cognitive and Systems Neuroscience Laboratory - Vinod Menon

  • Start year: Jan. 2016

  • Partners: Athena project-team,

  • See also: http://www-sop.inria.fr/members/Demian.Wassermann/large-brain-nets.html

  • In the past two decades, brain imaging of neurotypical individuals and clinical populations has primarily focused on localization of function and structures in the brain, revealing activation in specific brain regions during performance of cognitive tasks through modalities such as functional MRI. In parallel, technologies to identify white matter structures have been developed using diffusion MRI. More recently, interest has shifted towards developing a deeper understanding of the brain's intrinsic architecture and its influence on cognitive and affective information processing. Using for this resting state fMRI and diffusion MRI to build the functional and structural networks of the human brain.

    The human brain is a complex patchwork of interconnected regions, and graph-theoretical approaches have become increasingly useful for understanding how functionally connected systems engender, and constrain, cognitive functions. The functional nodes of the human brain and their structural inter-connectivity, collectively the "connectome", are, however, poorly understood. Critically, there is a dearth of computational methods for reliably identifying functional nodes of the brain and their structural inter-connectivity in vivo, despite an abundance of high-quality data from the Human Connectome Project (HCP). Devising and validating methods for investigating the human connectome has therefore taken added significance.

    The first major goal of this project is to develop and validate appropriate sophisticated computational and mathematical tools for identifying functional nodes at the whole-brain level and measuring structural and functional connectivity between them, using state-of-the-art human brain imaging techniques and open-source HCP data. To this end, we will first develop and validate novel computational tools for (1) identifying stable functional nodes of the human brain using resting-state functional MRI and (2) measuring structural connectivity between functional nodes of the brain using multi-shell high-angular diffusion MRI. Due to the complementarity of the two imaging techniques fMRI and dMRI, our novel computational methods methods, the synergy between the two laboratories of this associate team will allow us to reveal in unprecedented detail the structural and functional connectivity of the human brain.

    The second major goal of this project is to use our newly developed computational tools to characterize normal structural and functional brain networks in neurotypical adults.

Inria International Partners

Informal International Partners
  • SCIL Laboratory, Sherbrooke University, CA (Maxime Descoteaux)

  • CMRR, University of Minnesota, USA (Christophe Lenglet)

  • Verona University, It (Gloria Menegaz)

  • Department of CISE, the University of Florida, Gainesville, USA (Baba C. Vemuri)

  • Centre for Medical Image Computing (CMIC), Dept. Computer Science, UCL, UK (D. Alexander)

  • SBIA, University of Pennsylvania Medical School, USA (R. Verma).

  • University Houari Boumedienne (USTHB, Algiers) (L. Boumghar) and University of Boumerdes, (D. Cherifi), Algeria.

  • BESA company on EEG/MEG modeling.

  • CRM, Centre de Recherche Mathématiques, Montréal, Canada.

Participation in Other International Programs

Program: Collaborative Research in Computational Neuroscience (NSF – ANR)
  • Project acronym: NeuroRef

  • Project title: Building MRI Reference Atlases to Analyze Brain Trauma and Post‐ Traumatic Stress

  • Start date: 2016-10-01, End date: 2019-12-31

  • P.I : D. Wassermann (Athena) – S. Bouix (Harvard Medcical School)

  • Partners: Athena project-team,

  • International Partner (Institution - Laboratory - Researcher):

    • Harvard Medical School (United States) - Psychiatry and Neuroimaging Lab - Sylvain Bouix

  • Abstract:

    While mild traumatic brain injury (mTBI) has become the focus of many neuroimaging studies, the understanding of mTBI, particularly in patients who evince no radiological evidence of injury and yet experience clinical and cognitive symptoms, has remained a complex challenge. Sophisticated imaging tools are needed to delineate the kind of subtle brain injury that is extant in these patients, as existing tools are often ill-suited for the diagnosis of mTBI. For example, conventional magnetic resonance imaging (MRI) studies have focused on seeking a spatially consistent pattern of abnormal signal using statistical analyses that compare average differences between groups, i.e., separating mTBI from healthy controls. While these methods are successful in many diseases, they are not as useful in mTBI, where brain injuries are spatially heterogeneous. The goal of this proposal is to develop a robust framework to perform subject-specific neuroimaging analyses of Diffusion MRI (dMRI), as this modality has shown excellent sensitivity to brain injuries and can locate subtle brain abnormalities that are not detected using routine clinical neuroradiological readings. New algorithms will be developed to create Individualized Brain Abnormality (IBA) maps that will have a number of clinical and research applications. In this proposal, this technology will be used to analyze a previously acquired dataset from the INTRuST Clinical Consortium, a multi-center effort to study subjects with Post- Traumatic Stress Disorder (PTSD) and mTBI. Neuroimaging abnormality measures will be linked to clinical and neuropsychological assessments. This technique will allow us to tease apart neuroimaging differences between PTSD and mTBI and to establish baseline relationships between neuroimaging markers, and clinical and cognitive measures. Upon completion of this project, a set of tools, which have the potential to establish radiological evidence of brain injury in mTBI, will have been designed and evaluated, thereby enhancing both the diagnosis and monitoring of progression/recovery of injury, as well assessing the efficacy of therapies on the injured brain.