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Microvascular Dysfunction and Whole-Brain White Matter Connectivity: The Maastricht Study
Magdalena Beran1,2,3, April C E van Gennip1,2, Coen D A Stehouwer1,2
1Department of Internal Medicine Maastricht University Medical Centre+ (MUMC+) Maastricht The Netherlands.
Microvascular dysfunction, indicated by indirect markers, does not appear to impact overall white matter connectivity in the brain. This study found no significant associations between various microvascular measures and brain connectivity metrics.
Area of Science:
- Neuroscience
- Vascular Biology
- Medical Imaging
Background:
- Microvascular dysfunction is implicated in cerebral disorders.
- Its role in disrupting white matter tracts and brain connectivity requires further investigation.
- This study explores the link between microvascular function biomarkers and brain connectivity.
Purpose of the Study:
- To investigate the association between multiple microvascular function biomarkers and whole-brain white matter connectivity.
- To determine if markers of endothelial dysfunction correlate with white matter network organization.
Main Methods:
- Utilized cross-sectional data from The Maastricht Study (n=4326).
- Assessed microvascular function via urinary albumin excretion, retinal vessel calibers, dilation responses, and plasma endothelial dysfunction biomarkers.
- Quantified white matter connectivity using 3T diffusion MRI, analyzing measures like characteristic path length and global efficiency.
Main Results:
- A composite score of endothelial dysfunction biomarkers showed a nonsignificant association with longer characteristic path length after multiple comparison correction.
- No significant associations were found between other microvascular function measures and any white matter connectivity metrics.
- The study adjusted for sociodemographic, lifestyle, and cardiovascular factors.
Conclusions:
- Indirect markers of microvascular dysfunction are not associated with whole-brain white matter connectivity.
- These findings suggest a lack of a direct link between the measured microvascular health and the structural organization of white matter networks.
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