| Literature DB >> 31500909 |
Nick A Weaver1, Thomas Doeven2, Frederik Barkhof3, J Matthijs Biesbroek2, Onno N Groeneveld2, Hugo J Kuijf4, Niels D Prins5, Philip Scheltens6, Charlotte E Teunissen7, Wiesje M van der Flier8, Geert Jan Biessels2.
Abstract
White matter hyperintensities (WMHs) are a common manifestation of cerebral small vessel disease. WMHs are also frequently observed in patients with familial and sporadic Alzheimer's disease, often with a particular posterior predominance. Whether amyloid and tau pathologies are linked to WMH occurrence is still debated. We examined whether cerebral amyloid and tau burden, reflected in cerebrospinal fluid amyloid-beta 1-42 (Aβ-42) and phosphorylated tau (p-tau), are related to WMH location in a cohort of 517 memory clinic patients. Two lesion mapping techniques were performed: voxel-based analyses and region of interest-based linear regression. Voxelwise associations were found between lower Aβ-42 and parieto-occipital periventricular WMHs. Regression analyses demonstrated that lower Aβ-42 correlated with larger WMH volumes in the splenium of the corpus callosum and posterior thalamic radiation, also after controlling for markers of vascular disease. P-tau was not consistently related to WMH occurrence. Our findings indicate that cerebral amyloid burden is associated with WMHs located in specific posterior white matter regions, possibly reflecting region-specific effects of amyloid pathology on the white matter.Entities:
Keywords: Alzheimer's disease; Amyloid-beta; Cerebrospinal fluid; Lesion mapping; Magnetic resonance imaging; Tau; White matter hyperintensities
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Year: 2019 PMID: 31500909 DOI: 10.1016/j.neurobiolaging.2019.08.001
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673