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Updated: Aug 27, 2026

An In Vivo Blood-brain Barrier Permeability Assay in Mice Using Fluorescently Labeled Tracers
Published on: February 26, 2018
EXPRESS: Disentangling MRI-derived blood-brain barrier leakage into vascular permeability and surface area
Damon Verstappen1,2, Joost J A de Jong1,2, Paulien H Voorter1,2
1Department of Radiology & Nuclear Medicine, Maastricht University Medical Centre+, Maastricht, Netherlands.
Background:
In neurovascular and neurodegenerative diseases, blood-brain barrier (BBB) disruption can be subtle, diffuse, and MRI-derived measures are confounded by microvascular architecture. Therefore, we aimed to disentangle MRI-derived blood-brain barrier leakage rate (Ki) into intrinsic vascular permeability (P) and surface area (S).
Methods:
In this cross-sectional study, 45 patients with cSVD and 26 elderly controls underwent dynamic contrast-enhanced (DCE) MRI to determine Ki and vessel architecture imaging (VAI) to estimate S. These measures were used to calculate P.
Results:
Compared to normal-appearing white matter (NAWM), Ki was higher in WMH (β=0.297, p<0.001) and deep gray matter (DGM) (β=0.210, p=0.007). P was higher in WMH (β=0.410, p<0.001) and similar between NAWM and DGM. S was smaller in WMH (β=-0.467, p<0.001) and larger in DGM (β=0.540, p<0.001). Ki (β=0.289, p=0.007) and P (β=0.249, p=0.021) were only higher in patients than controls in concentric shells surrounding WMH. S was smaller in WMH of patients than controls (β=-0.085, p=0.049). With age, Ki (β=0.260, p=0.008) and P increased (β=0.273, p<0.001), while S decreased (β=-0.079, p=0.025).
Conclusion:
Disentangling P and S from the BBB leakage rate provides two biologically more specific and interpretable measures, which have counteracting effects on the BBB leakage in aging and disease.
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