Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: applied to GENFI study
Claire CuryiD, Stanley DurrlemaniD, David M. CashiD, Marco LorenziiD, Jennifer M. NicholasiD, Martina BocchettaiD, John Cornelis Van SwieteniD, Barbara BorroniiD, Daniela GalimbertiiD, Mario MasellisiD, Maria Carmela TartagliaiD, James Benedict RoweiD, Caroline GraffiD, Fabrizio TagliaviniiD, Giovanni Battista FrisoniiD, Robert Jr LaforceiD, Elizabeth C. FingeriD, Alexandre de MendonçaiD, Sandro SorbiiD, Sebastien Ourselin AiD, Jonathan Daniel RohreriD, Marc Modat AiD, on behalf of the Genetic FTD Initiative, GENFI
Abstract
Brain atrophy as measured from structural MR images, is one of the primary imaging biomarkers used to track neurodegenerative disease progression. In diseases such as frontotemporal dementia or Alzheimers disease, atrophy can be observed in key brain structures years before any clinical symptoms are present. Atrophy is most commonly captured as volume change of key structures and the shape changes of these structures are typically not analysed despite being potentially more sensitive than summary volume statistics over the entire structure.\n\nIn this paper we propose a spatiotemporal analysis pipeline based Large Diffeomorphic Deformation Metric Mapping (LDDMM) to detect shape changes from volumetric MRI scans. We applied our framework to a cohort of individuals with genetic variants of frontotemporal dementia and healthy controls from the Genetic FTD Initiative (GENFI) study. Our method, take full advantage of the LDDMM framework, and relies on the creation of a population specific average spatiotemporal trajectory of a relevant brain structure of interest, the thalamus in our case. The residuals from each patient data to the average spatiotemporal trajectory are then clustered and studied to assess when presymptomatic mutation carriers differ from healthy control subjects.\n\nWe found statistical differences in shape in the anterior region of the thalamus at least five years before the mutation carrier subjects develop any clinical symptoms. This region of the thalamus has been shown to be predominantly connected to the frontal lobe, consistent with the pattern of cortical atrophy seen in the disease.
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