4.7 Article

Colocalization of cerebral iron with Amyloid beta in Mild Cognitive Impairment

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SCIENTIFIC REPORTS
卷 6, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/srep35514

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  1. Swiss National Science Foundation (Schweizerischer Nationalfonds, SNF)
  2. Clinical Research Priority Program (CRPP) of the University of Zurich on Molecular Imaging (MINZ)
  3. National Institutes of Health (NIBIB) [P41 EB015909]
  4. ETH Zurich, Switzerland

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Quantitative Susceptibility Mapping (QSM) MRI at 7 Tesla and 11-Carbon Pittsburgh-Compound-B PET were used for investigating the relationship between brain iron and Amyloid beta (A beta) plaqueload in a context of increased risk for Alzheimer's disease (AD), as reflected by the Apolipoprotein E epsilon 4 (APOE-e4) allele and mild cognitive impairment (MCI) in elderly subjects. Carriers of APOE-e4 with normal cognition had higher cortical A beta-plaque-load than non-carriers. In MCI an association between APOE-e4 and higher A beta-plaque-load was observable both for cortical and subcortical brain-regions. APOE-e4 and MCI was also associated with higher cortical iron. Moreover, cerebral iron significantly affected functional coupling, and was furthermore associated with increased A beta-plaque-load (R-2-adjusted = 0.80, p < 0.001) and APOE-e4 carrier status (p < 0.001) in MCI. This study confirms earlier reports on an association between increased brain iron-burden and risk for neurocognitive dysfunction due to AD, and indicates that disease-progression is conferred by spatial colocalization of brain iron deposits with A beta-plaques.

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