<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ying Y</submitter><funding>US National Institutes of Health</funding><funding>Science and Technology Commission of Shanghai Municipality</funding><funding>Shanghai Municipal Health Commission</funding><funding>National Natural Science Foundation of China</funding><funding>NINDS NIH HHS</funding><pagination>4527-4539</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11247670</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(7)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>We explored how blood-brain barrier (BBB) leakage rate of gadolinium chelates (K&lt;sup>trans&lt;/sup>) and BBB water exchange rate (k&lt;sub>w&lt;/sub>) varied in cerebral small vessel disease (cSVD) subtypes.&lt;h4>Methods&lt;/h4>Thirty sporadic cSVD, 40 cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), and 13 high-temperature requirement factor A serine peptidase 1 (HTRA) -related cSVD subjects were investigated parallel to 40 healthy individuals. Subjects underwent clinical, cognitive, and MRI assessment.&lt;h4>Results&lt;/h4>In CADASIL, no difference in K&lt;sup>trans&lt;/sup>, but lower k&lt;sub>w&lt;/sub> was observed in multiple brain regions. In sporadic cSVD, no difference in k&lt;sub>w&lt;/sub>, but higher K&lt;sup>trans&lt;/sup> was found in the whole b</pubmed_abstract><journal>Alzheimer's &amp; dementia : the journal of the Alzheimer's Association</journal><pubmed_title>Heterogeneous blood-brain barrier dysfunction in cerebral small vessel diseases.</pubmed_title><pmcid>PMC11247670</pmcid><funding_grant_id>2022XD022</funding_grant_id><funding_grant_id>92249301</funding_grant_id><funding_grant_id>20Z11900802</funding_grant_id><funding_grant_id>82025018</funding_grant_id><funding_grant_id>R01 NS114382</funding_grant_id><funding_grant_id>82271352</funding_grant_id><funding_grant_id>R01NS114382</funding_grant_id><funding_grant_id>81961128030</funding_grant_id><funding_grant_id>81971123</funding_grant_id><pubmed_authors>Chabriat H</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Shao X</pubmed_authors><pubmed_authors>Wang DJJ</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Ying Y</pubmed_authors><pubmed_authors>Yao T</pubmed_authors><pubmed_authors>Montagne A</pubmed_authors><pubmed_authors>Yang Q</pubmed_authors><pubmed_authors>Tang W</pubmed_authors><pubmed_authors>Cheng X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Heterogeneous blood-brain barrier dysfunction in cerebral small vessel diseases.</name><description>&lt;h4>Introduction&lt;/h4>We explored how blood-brain barrier (BBB) leakage rate of gadolinium chelates (K&lt;sup>trans&lt;/sup>) and BBB water exchange rate (k&lt;sub>w&lt;/sub>) varied in cerebral small vessel disease (cSVD) subtypes.&lt;h4>Methods&lt;/h4>Thirty sporadic cSVD, 40 cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), and 13 high-temperature requirement factor A serine peptidase 1 (HTRA) -related cSVD subjects were investigated parallel to 40 healthy individuals. Subjects underwent clinical, cognitive, and MRI assessment.&lt;h4>Results&lt;/h4>In CADASIL, no difference in K&lt;sup>trans&lt;/sup>, but lower k&lt;sub>w&lt;/sub> was observed in multiple brain regions. In sporadic cSVD, no difference in k&lt;sub>w&lt;/sub>, but higher K&lt;sup>trans&lt;/sup> was found in the whole b</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2025-04-25T19:12:19.618Z</modification><creation>2025-04-06T07:54:36.617Z</creation></dates><accession>S-EPMC11247670</accession><cross_references><pubmed>38787758</pubmed><doi>10.1002/alz.13874</doi></cross_references></HashMap>