<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Walsh J</submitter><funding>NHS Trust NIHR Biomedical Research centre</funding><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><funding>National Institute for Health Research Clinical Research Network</funding><pagination>1361-1371</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8874873</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>144(5)</volume><pubmed_abstract>Cerebral small vessel disease (SVD) is a major cause of stroke and dementia. The underlying pathogenesis is poorly understood, but both neuroinflammation and increased blood-brain barrier permeability have been hypothesized to play a role, and preclinical studies suggest the two processes may be linked. We used PET magnetic resonance to simultaneously measure microglial activation using the translocator protein radioligand 11C-PK11195, and blood-brain barrier permeability using dynamic contrast enhanced MRI. A case control design was used with two disease groups with sporadic SVD (n = 20), monogenic SVD (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, CADASIL), and normal controls (n = 20) were studied. Hotspots of increased glial activation and </pubmed_abstract><journal>Brain : a journal of neurology</journal><pubmed_title>Microglial activation and blood-brain barrier permeability in cerebral small vessel disease.</pubmed_title><pmcid>PMC8874873</pmcid><funding_grant_id>NF-SI-0617-10006</funding_grant_id><funding_grant_id>MR/M024873/1</funding_grant_id><funding_grant_id>MR/N026896/1</funding_grant_id><funding_grant_id>MR/M009041/1</funding_grant_id><funding_grant_id>MR/K02308X/1</funding_grant_id><pubmed_authors>Fryer TD</pubmed_authors><pubmed_authors>Tozer DJ</pubmed_authors><pubmed_authors>Sari H</pubmed_authors><pubmed_authors>Hong YT</pubmed_authors><pubmed_authors>Shah NJ</pubmed_authors><pubmed_authors>Rosenberg G</pubmed_authors><pubmed_authors>Drazyk A</pubmed_authors><pubmed_authors>O'Brien JT</pubmed_authors><pubmed_authors>Markus HS</pubmed_authors><pubmed_authors>Walsh J</pubmed_authors><pubmed_authors>Williams G</pubmed_authors><pubmed_authors>Aigbirhio FI</pubmed_authors></additional><is_claimable>false</is_claimable><name>Microglial activation and blood-brain barrier permeability in cerebral small vessel disease.</name><description>Cerebral small vessel disease (SVD) is a major cause of stroke and dementia. The underlying pathogenesis is poorly understood, but both neuroinflammation and increased blood-brain barrier permeability have been hypothesized to play a role, and preclinical studies suggest the two processes may be linked. We used PET magnetic resonance to simultaneously measure microglial activation using the translocator protein radioligand 11C-PK11195, and blood-brain barrier permeability using dynamic contrast enhanced MRI. A case control design was used with two disease groups with sporadic SVD (n = 20), monogenic SVD (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, CADASIL), and normal controls (n = 20) were studied. Hotspots of increased glial activation and </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jun</publication><modification>2025-04-21T23:16:11.858Z</modification><creation>2025-04-05T19:05:19.457Z</creation></dates><accession>S-EPMC8874873</accession><cross_references><pubmed>34000009</pubmed><doi>10.1093/brain/awab003</doi></cross_references></HashMap>