Blood–Brain Barrier Leakage Is Increased in Parkinson’s Disease

Blood-brain barrier (BBB) disruption has been noted in animal models of Parkinson's disease (PD) and forms the basis of the vascular hypothesis of neurodegeneration, yet clinical studies are lacking. To determine alterations in BBB integrity in PD, with comparison to cerebrovascular disease. Dy...

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Published inFrontiers in physiology Vol. 11; p. 593026
Main Authors Al-Bachari, Sarah, Naish, Josephine H., Parker, Geoff J. M., Emsley, Hedley C. A., Parkes, Laura M.
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 22.12.2020
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Summary:Blood-brain barrier (BBB) disruption has been noted in animal models of Parkinson's disease (PD) and forms the basis of the vascular hypothesis of neurodegeneration, yet clinical studies are lacking. To determine alterations in BBB integrity in PD, with comparison to cerebrovascular disease. Dynamic contrast enhanced magnetic resonance images were collected from 49 PD patients, 15 control subjects with cerebrovascular disease [control positive (CP)] and 31 healthy control subjects [control negative (CN)], with all groups matched for age. Quantitative maps of the contrast agent transfer coefficient across the BBB ( ) and plasma volume (v ) were produced using Patlak analysis. Differences in and v were assessed with voxel-based analysis as well as in regions associated with PD pathophysiology. In addition, the volume of white matter lesions (WMLs) was obtained from T -weighted fluid attenuation inversion recovery (FLAIR) images. Higher , reflecting higher BBB leakage, was found in the PD group than in the CN group using voxel-based analysis; differences were most prominent in the posterior white matter regions. Region of interest analysis confirmed to be significantly higher in PD than in CN, predominantly driven by differences in the substantia nigra, normal-appearing white matter, WML and the posterior cortex. WML volume was significantly higher in PD compared to CN. values and WML volume were similar in PD and CP, suggesting a similar burden of cerebrovascular disease despite lower cardiovascular risk factors. These results show BBB disruption in PD.
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This article was submitted to Vascular Physiology, a section of the journal Frontiers in Physiology
Reviewed by: Axel Montagne, University of Southern California, Los Angeles, United States; Walter Backes, Maastricht University Medical Centre, Netherlands
Edited by: Fabrice Dabertrand, University of Colorado, United States
ISSN:1664-042X
1664-042X
DOI:10.3389/fphys.2020.593026