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Cerebral amyloid burden is associated with white matter hyperintensity location in specific posterior white matter regions.
Weaver, Nick A; Doeven, Thomas; Barkhof, Frederik; Biesbroek, J Matthijs; Groeneveld, Onno N; Kuijf, Hugo J; Prins, Niels D; Scheltens, Philip; Teunissen, Charlotte E; van der Flier, Wiesje M; Biessels, Geert Jan.
Afiliação
  • Weaver NA; Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, the Netherlands. Electronic address: n.a.weaver@umcutrecht.nl.
  • Doeven T; Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, the Netherlands.
  • Barkhof F; Institutes of Neurology and Healthcare Engineering, UCL, London, UK; Department of Radiology and Nuclear Medicine, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands.
  • Biesbroek JM; Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, the Netherlands.
  • Groeneveld ON; Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, the Netherlands.
  • Kuijf HJ; Image Sciences Institute, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Prins ND; Brain Research Center, Amsterdam, the Netherlands; Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands.
  • Scheltens P; Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands.
  • Teunissen CE; Neurochemistry Lab and Biobank, Department of Clinical Chemistry, Amsterdam Neuroscience, VU University Medical Center Amsterdam, Amsterdam, the Netherlands.
  • van der Flier WM; Alzheimer Center Amsterdam, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands; Department of Epidemiology and Biostatistics, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, the Netherlands.
  • Biessels GJ; Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, the Netherlands.
Neurobiol Aging ; 84: 225-234, 2019 12.
Article em En | MEDLINE | ID: mdl-31500909
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 (Aß-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 Aß-42 and parieto-occipital periventricular WMHs. Regression analyses demonstrated that lower Aß-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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Peptídeos beta-Amiloides / Doença de Alzheimer / Substância Branca Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fragmentos de Peptídeos / Peptídeos beta-Amiloides / Doença de Alzheimer / Substância Branca Idioma: En Ano de publicação: 2019 Tipo de documento: Article