Language and spatial dysfunction in Alzheimer disease with white matter thorn-shaped astrocytes

OBJECTIVESAlzheimer disease (AD) shows a broad array of clinical presentations, but the mechanisms underlying these phenotypic variants remain elusive. Aging-related astrogliopathy (ARTAG) is a relatively recent term encompassing a broad array of tau deposition in astroglia outside the range of trad...

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Veröffentlicht in:Neurology 2020-03, Vol.94 (13), p.e1353-e1364
Hauptverfasser: Resende, Elisa de Paula França, Nolan, Amber L., Petersen, Cathrine, Ehrenberg, Alexander J., Spina, Salvatore, Allen, Isabel E., Rosen, Howard J., Kramer, Joel, Miller, Bruce L., Seeley, William W., Gorno-Tempini, Maria Luiza, Miller, Zachary, Grinberg, Lea T.
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Sprache:eng
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Zusammenfassung:OBJECTIVESAlzheimer disease (AD) shows a broad array of clinical presentations, but the mechanisms underlying these phenotypic variants remain elusive. Aging-related astrogliopathy (ARTAG) is a relatively recent term encompassing a broad array of tau deposition in astroglia outside the range of traditional tauopathies. White matter thorn-shaped astrocyte (WM-TSA) clusters, a specific ARTAG subtype, has been associated with atypical language presentation of AD in a small study lacking replication. To interrogate the impact of WM-TSA in modifying clinical phenotype in AD, we investigated a clinicopathologic sample of 83 persons with pure cortical AD pathology and heterogeneous clinical presentations. METHODSWe mapped WM-TSA presence and density throughout cortical areas and interrogated whether WM-TSA correlated with atypical AD presentation or worse performance in neuropsychological testing. RESULTSWM-TSA was present in nearly half of the cases and equally distributed in typical and atypical AD presentations. Worsening language and visuospatial functions were correlated with higher WM-TSA density in language-related and visuospatial-related regions, respectively. These findings were unrelated to regional neurofibrillary tangle burden. Next, unsupervised clustering divided the participants into 2 groupsa high–WM-TSA (n = 9) and low–WM-TSA (n = 74) pathology signature. The high–WM-TSA group scored significantly worse in language but not in other cognitive domains. CONCLUSIONSThe negative impact of WM-TSA pathology to language and possibly visuospatial networks suggests that WM-TSA is not as benign as other ARTAG types and may be explored as a framework to understand the mechanisms and impact of astrocytic tau deposition in AD in humans.
ISSN:0028-3878
1526-632X
DOI:10.1212/WNL.0000000000008937