%0 Journal Article %A Andre Altmann %A David M Cash %A Martina Bocchetta %A Carolin Heller %A Regina Reynolds %A Katrina Moore %A Rhian S Convery %A David L Thomas %A John van Swieten %A Fermin Moreno %A Raquel Sanchez-Valle %A Barbara Borroni %A Robert Laforce, Jr %A Mario Masellis %A Maria Carmela Tartaglia %A Caroline Graff %A Daniela Galimberti %A James B. Rowe %A Elizabeth Finger %A Matthis Synofzik %A Rik Vandenberghe %A Alexandre de Mendonça %A Fabrizio Tagliavini %A Isabel Santana %A Simon Ducharme %A Chris Butler %A Alex Gerhard %A Johannes Levin %A Adrian Danek %A Giovanni Frisoni %A Roberta Ghidoni %A Sandro Sorbi %A Markus Otto %A Mina Ryten %A Jonathan D Rohrer %A on behalf of the Genetic FTD Initiative, GENFI. %T Analysis of brain atrophy and local gene expression implicates astrocytes in Frontotemporal dementia %D 2019 %R 10.1101/2019.12.11.872143 %J bioRxiv %P 2019.12.11.872143 %X Frontotemporal dementia (FTD) is a heterogeneous neurodegenerative disorder characterized by neuronal loss in the frontal and temporal lobes. Despite progress in understanding which genes are associated with the aetiology of FTD (C9orf72, GRN and MAPT), the biological basis of how mutations in these genes lead to cell loss in specific cortical regions remains unclear. In this work we combined gene expression data for 16,912 genes from the Allen Institute for Brain Science atlas with brain maps of gray matter atrophy in symptomatic C9orf72, GRN and MAPT carriers obtained from the Genetic FTD Initiative study. A set of 405 and 250 genes showed significant positive and negative correlation, respectively, with atrophy patterns in all three maps. The gene set with increased expression in spared cortical regions, i.e., signaling regional resilience to atrophy, is enriched for neuronal genes, while the gene set with increased expression in atrophied regions, i.e., signaling regional vulnerability, is enriched for astrocyte genes. Notably, these results extend earlier findings from proteomic analyses in the same cortical regions of interest comparing healthy controls and patients with FTD. Thus, our analysis indicates that cortical regions showing the most severe atrophy in genetic FTD are those with the highest astrocyte density in healthy subjects. Therefore, astrocytes may play a more active role in the onset of neurodegeneration in FTD than previously assumed, e.g., through emergence of neurotoxic (A1) astrocytes.Abbreviated summary Altmann et al. investigated the concordance between spatial cortical gene expression in healthy subjects and atrophy patterns in genetic frontotemporal dementia. They found that gene expression of astrocyte-related genes was higher in regions with atrophy. Thus, suggesting a more active role of astrocytes in the onset of neurodegeneration.AIBSAllen Institute for Brain ScienceC9orf72Chromosome 9 open reading frame 72 geneEWCEExpression Weighted Cell-type EnrichmentFTDFrontotemporal dementiaGENFIGenetic FTD InitiativeGFAPglial fibrillary acidic proteinGOGene OntologyGRNProgrenulin geneLMELinear Mixed EffectsLSDLysosomal Storage DisorderMAPTtau geneMNIMontreal Neurological Institute and HospitalNCLneuronal ceroid lipofuscinosisOROdds RatioVBMVoxel Based Morphometry %U https://www.biorxiv.org/content/biorxiv/early/2019/12/12/2019.12.11.872143.full.pdf