Metabolic and Vascular Imaging Biomarkers in Down Syndrome Provide Unique Insights Into Brain Aging and Alzheimer Disease Pathogenesis
People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD). Neuropathology consistent with AD is present by 40 years of age and dementia may develop up to a decade later. In this review, we describe metabolic and vascular neuroimaging studies in DS that suggest these funct...
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doaj-8a8b996e30044926b6fcfc8b981bceb52020-11-25T00:48:37ZengFrontiers Media S.A.Frontiers in Aging Neuroscience1663-43652018-06-011010.3389/fnagi.2018.00191382293Metabolic and Vascular Imaging Biomarkers in Down Syndrome Provide Unique Insights Into Brain Aging and Alzheimer Disease PathogenesisElizabeth Head0David K. Powell1Frederick A. Schmitt2Department of Pharmacology & Nutritional Sciences, Sanders Brown Center on Aging, University of Kentucky, Lexington, KY, United StatesMagnetic Resonance Imaging and Spectroscopy Center, Sanders Brown Center on Aging, University of Kentucky, Lexington, KY, United StatesDepartment of Neurology, Sanders Brown Center on Aging, University of Kentucky, Lexington, KY, United StatesPeople with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD). Neuropathology consistent with AD is present by 40 years of age and dementia may develop up to a decade later. In this review, we describe metabolic and vascular neuroimaging studies in DS that suggest these functional changes are a key feature of aging, linked to cognitive decline and AD in this vulnerable cohort. FDG-PET imaging in DS suggests systematic reductions in glucose metabolism in posterior cingulate and parietotemporal cortex. Magentic resonance spectroscopy studies show consistent decreases in neuronal health and increased myoinositol, suggesting inflammation. There are few vascular imaging studies in DS suggesting a gap in our knowledge. Future studies would benefit from longitudinal measures and combining various imaging approaches to identify early signs of dementia in DS that may be amenable to intervention.https://www.frontiersin.org/article/10.3389/fnagi.2018.00191/fulldementiaFDG-PEThypometabolismhypermetabolismmyoinositolMR spectroscopy |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Elizabeth Head David K. Powell Frederick A. Schmitt |
spellingShingle |
Elizabeth Head David K. Powell Frederick A. Schmitt Metabolic and Vascular Imaging Biomarkers in Down Syndrome Provide Unique Insights Into Brain Aging and Alzheimer Disease Pathogenesis Frontiers in Aging Neuroscience dementia FDG-PET hypometabolism hypermetabolism myoinositol MR spectroscopy |
author_facet |
Elizabeth Head David K. Powell Frederick A. Schmitt |
author_sort |
Elizabeth Head |
title |
Metabolic and Vascular Imaging Biomarkers in Down Syndrome Provide Unique Insights Into Brain Aging and Alzheimer Disease Pathogenesis |
title_short |
Metabolic and Vascular Imaging Biomarkers in Down Syndrome Provide Unique Insights Into Brain Aging and Alzheimer Disease Pathogenesis |
title_full |
Metabolic and Vascular Imaging Biomarkers in Down Syndrome Provide Unique Insights Into Brain Aging and Alzheimer Disease Pathogenesis |
title_fullStr |
Metabolic and Vascular Imaging Biomarkers in Down Syndrome Provide Unique Insights Into Brain Aging and Alzheimer Disease Pathogenesis |
title_full_unstemmed |
Metabolic and Vascular Imaging Biomarkers in Down Syndrome Provide Unique Insights Into Brain Aging and Alzheimer Disease Pathogenesis |
title_sort |
metabolic and vascular imaging biomarkers in down syndrome provide unique insights into brain aging and alzheimer disease pathogenesis |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Aging Neuroscience |
issn |
1663-4365 |
publishDate |
2018-06-01 |
description |
People with Down syndrome (DS) are at high risk for developing Alzheimer disease (AD). Neuropathology consistent with AD is present by 40 years of age and dementia may develop up to a decade later. In this review, we describe metabolic and vascular neuroimaging studies in DS that suggest these functional changes are a key feature of aging, linked to cognitive decline and AD in this vulnerable cohort. FDG-PET imaging in DS suggests systematic reductions in glucose metabolism in posterior cingulate and parietotemporal cortex. Magentic resonance spectroscopy studies show consistent decreases in neuronal health and increased myoinositol, suggesting inflammation. There are few vascular imaging studies in DS suggesting a gap in our knowledge. Future studies would benefit from longitudinal measures and combining various imaging approaches to identify early signs of dementia in DS that may be amenable to intervention. |
topic |
dementia FDG-PET hypometabolism hypermetabolism myoinositol MR spectroscopy |
url |
https://www.frontiersin.org/article/10.3389/fnagi.2018.00191/full |
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