Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: applied to GENFI study

Author:

Cury ClaireORCID,Durrleman Stanley,Cash David,Lorenzi MarcoORCID,Nicholas Jennifer M,Bocchetta Martina,van Swieten John C.,Borroni Barbara,Galimberti Daniela,Masellis Mario,Carmela Tartaglia Maria,Rowe James B,Graff Caroline,Tagliavini Fabrizio,Frisoni Giovanni B.,Laforce Robert,Finger Elizabeth,de Mendonca Alexandre,Sorbi Sandro,Ourselin Sebastien,Rohrer Jonathan D.,Modat Marc,

Abstract

AbstractBrain 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 Alzheimer’s 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.In 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.We 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.

Publisher

Cold Spring Harbor Laboratory

Reference32 articles.

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