Fig. 5From: Frontotemporal lobar degeneration proteinopathies have disparate microscopic patterns of white and grey matter pathologyRegional distribution of WM and adjacent GM pathology burden in clinicopathological groups. Plots portray the regional distribution of WM and GM pathology burden in clinicopathological groups, i.e. a PPA with FTLD-Tau (nonfluent/agrammatic variant, naPPA) and PPA with FTLD-TDP (semantic variant, svPPA), and b bvFTD with FTLD-Tau and bvFTD with FTLD-TDP. The color scale represents least-square means of ln-transformed WM and GM %AO in each region derived from linear-mixed effects (LME) models adjusting for demographics. Asterisks denote areas of peak pathology burden. Legend: %AO = percentage area occupied by pathology; ACG = anterior cingulate gyrus; ANG = angular gyrus; bvFTD = behavioral variant of frontotemporal dementia; FTLD-Tau = frontotemporal lobar degeneration with inclusions of the tau protein; FTLD-TDP = frontotemporal lobar degeneration with inclusions of the TDP-43 protein; GM = grey matter; MFC = middle frontal cortex; naPPA = nonfluent/agrammatic variant of primary progressive aphasia; OFC = orbitofrontal cortex; STG = superior temporal gyrus; svPPA; semantic variant of primary progressive aphasia; WM = white matterBack to article page