Cerebral amyloid burden is associated with white matter hyperintensity location in specific posterior white matter regions
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2019-12
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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.
Keywords
Alzheimer's disease, Amyloid-beta, Cerebrospinal fluid, Lesion mapping, Magnetic resonance imaging, Tau, White matter hyperintensities, Clinical Neurology, Geriatrics and Gerontology, Ageing, General Neuroscience, Developmental Biology, Journal Article
Citation
Weaver, N A, Doeven, T, Barkhof, F, Biesbroek, J M, Groeneveld, O N, Kuijf, H J, Daniël Prins, N, Scheltens, P, Teunissen, C E, van der Flier, W M, Biessels, G J & TRACE-VCI study group 2019, 'Cerebral amyloid burden is associated with white matter hyperintensity location in specific posterior white matter regions', Neurobiology of Aging, vol. 84, pp. 225-234. https://doi.org/10.1016/j.neurobiolaging.2019.08.001