Metabolic syndrome severity score associates with structural brain features and functional connectivity of Default Mode Network subsystems in the HABS‐HD study
Background States of altered metabolic health such as metabolic syndrome (MetS), obesity, and insulin resistance increase Alzheimer’s Disease (AD) risk. Individuals with these conditions, like those with AD, have demonstrated changes in the structural and functional features of the Default Mode Netw...
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Veröffentlicht in: | Alzheimer's & dementia 2024-12, Vol.20 (S2), p.n/a |
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Sprache: | eng |
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Zusammenfassung: | Background
States of altered metabolic health such as metabolic syndrome (MetS), obesity, and insulin resistance increase Alzheimer’s Disease (AD) risk. Individuals with these conditions, like those with AD, have demonstrated changes in the structural and functional features of the Default Mode Network (DMN). Here, we characterize associations between systemic metabolic dysfunction, brain structure (Cortical Thickness and Hippocampal Volume) and functional connectivity of DMN subnetworks.
Method
We leveraged data from the Health and Aging Brain Study: Health Disparities (HABS‐HD) dataset, an ongoing longitudinal study that characterizes AD biomarkers across diverse populations. Specifically, we used data from the initial visits of the Hispanic and Non‐Hispanic White (NHW) cohorts. Individuals were categorized as cognitively healthy (n=1192; age=66.1 years, 65% female) or cognitively impaired (n=307; age=67.4 years, 50% female). We used a continuous measure of metabolic risk (Mets‐Z) that is more sensitive and ethnicity‐specific than categorical definitions of MetS. Mets‐Z a weighted composite of systolic blood pressure, triglycerides, HDL cholesterol, glucose, and waist circumference. Structural measures were acquired using FreeSurfer. Functional connectivity was measured via resting‐state fMRI, and pre‐processed using FSL. We utilized both summary metrics (ROI‐based connectivity estimations) and voxel‐wise approaches (FSL’s randomise).
Result
MetS‐Z differed between diagnostic groups (t=‐2.387, p=.017) and between Hispanics and NHWs (t=‐11.864, p |
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ISSN: | 1552-5260 1552-5279 |
DOI: | 10.1002/alz.091808 |