Title | Metabolic syndrome and its components in relation to in vivo brain amyloid and neurodegeneration in late middle age. |
Publication Type | Journal Article |
Year of Publication | 2021 |
Authors | Palta P, Rippon B, Tahmi M, Sherwood G, Soto L, Ceballos F, Laing K, He H, Reitz C, Razlighi Q, Teresi JA, Moreno H, Brickman AM, Luchsinger JA |
Journal | Neurobiol Aging |
Volume | 97 |
Pagination | 89-96 |
Date Published | 2021 01 |
ISSN | 1558-1497 |
Keywords | Age Factors, Alzheimer Disease, Amyloid beta-Peptides, Aniline Compounds, Blood Glucose, Brain, Diffusion Tensor Imaging, Female, Hispanic or Latino, Humans, Male, Metabolic Syndrome, Middle Aged, Nerve Degeneration, New York, Risk, Stilbenes, Triglycerides |
Abstract | Metabolic syndrome (MetS) is associated with dementia, but it is unclear whether MetS is related to Alzheimer's disease (AD). We investigated the association of MetS with brain amyloid, a key AD feature, and neurodegeneration. A community-based sample of 350 middle-aged Hispanics in New York City had cerebral amyloid β (Aβ) burden ascertained with F-Florbetaben positron emission tomography. Neurodegeneration was ascertained as cortical thickness in AD signature regions from 3T brain MRI. MetS and its components (glucose, blood pressure, triglycerides, high-density lipoprotein, adiposity) were defined using the National Institutes of Health criteria. Neither the presence of MetS nor the MetS score was associated with Aβ or neurodegeneration. Among the MetS components, elevated glucose was associated with lower Aβ burden, and this association was not explained by diabetes treatment. Glucose and triglycerides were related to smaller cortical thickness. Our findings suggest that MetS as an arbitrary measure of aggregate metabolic and vascular risk does not capture the risk of AD neuropathology in late middle age and that other approaches to measure the aggregate risk should be examined. |
DOI | 10.1016/j.neurobiolaging.2020.09.023 |
Alternate Journal | Neurobiol Aging |
PubMed ID | 33166929 |
PubMed Central ID | PMC7810168 |
Grant List | R01 AG050440 / AG / NIA NIH HHS / United States K24 AG045334 / AG / NIA NIH HHS / United States P30 AG059303 / AG / NIA NIH HHS / United States P30 AG066462 / AG / NIA NIH HHS / United States UL1 TR001873 / TR / NCATS NIH HHS / United States K99 AG052830 / AG / NIA NIH HHS / United States R00 AG052830 / AG / NIA NIH HHS / United States RF1 AG051556 / AG / NIA NIH HHS / United States |
Related Institute:
Brain Health Imaging Institute (BHII)