Blood-brain barrier leakage hotspots collocating with brain lesions due to sporadic and monogenic small vessel disease

Author:

Rudilosso Salvatore1ORCID,Stringer Michael S2ORCID,Thrippleton Michael2,Chappell Francesca2,Blair Gordon W2,Jaime Garcia Daniela2,Doubal Fergus2,Hamilton Iona2,Janssen Esther3,Kopczak Anna4ORCID,Ingrisch Michael5,Kerkhofs Danielle6,Backes Walter H7,Staals Julie6,Duering Marco48ORCID,Dichgans Martin4910,Wardlaw Joanna M2ORCID,

Affiliation:

1. Comprehensive Stroke Center, Department of Neuroscience, Hospital Clinic and August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain

2. Centre for Clinical Brain Sciences, UK Dementia Research Institute, University of Edinburgh, Edinburgh, UK

3. Department of Neurology, Radboud University Medical Centre (Radboudumc), Nijmegen, The Netherlands

4. Institute for Stroke and Dementia Research, University Hospital, LMU Munich, Munich, Germany

5. Department of Radiology, University Hospital, LMU Munich, Munich, Germany

6. Department of Neurology and School for Cardiovascular Diseases (CARIM), Maastricht University Medical Center+, Maastricht, The Netherlands

7. Department of Radiology & Nuclear Medicine, Schools for Mental Health & Neuroscience and School for Cardiovascular Diseases, Maastricht University Medical Centre, Maastricht, Netherlands

8. Medical Image Analysis Center (MIAC AG) and Department of Biomedical Engineering, University of Basel, Basel, Switzerland

9. Munich Cluster for Systems Neurology, Munich, Germany

10. German Center for Neurodegenerative Diseases, Munich, Germany

Abstract

Blood-brain barrier (BBB) is known to be impaired in cerebral small vessel disease (SVD), and is measurable by dynamic-contrast enhancement (DCE)-MRI. In a cohort of 69 patients (42 sporadic, 27 monogenic SVD), who underwent 3T MRI, including DCE and cerebrovascular reactivity (CVR) sequences, we assessed the relationship of BBB-leakage hotspots to SVD lesions (lacunes, white matter hyperintensities (WMH), and microbleeds). We defined as hotspots the regions with permeability surface area product highest decile on DCE-derived maps within the white matter. We assessed factors associated with the presence and number of hotspots corresponding to SVD lesions in multivariable regression models adjusted for age, WMH volume, number of lacunes, and SVD type. We identified hotspots at lacune edges in 29/46 (63%) patients with lacunes, within WMH in 26/60 (43%) and at the WMH edges in 34/60 (57%) patients with WMH, and microbleed edges in 4/11 (36%) patients with microbleeds. In adjusted analysis, lower WMH-CVR was associated with presence and number of hotspots at lacune edges, and higher WMH volume with hotspots within WMH and at WMH edges, independently of the SVD type. In conclusion, SVD lesions frequently collocate with high BBB-leakage in patients with sporadic and monogenic forms of SVD.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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