<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhao M</submitter><funding>Vetenskapsrådet</funding><funding>UK Dementia Research Institute</funding><funding>Karolinska Institutet</funding><funding>National Natural Science Foundation of China</funding><funding>Swedish Foundation for International Cooperation in Research and Higher Education</funding><funding>Alzheimer&amp;apos;s Society</funding><funding>National Institutes of Health</funding><funding>Intramural Research Program</funding><funding>Alzheimer&amp;apos;s Association</funding><funding>Forskningsrådet om Hälsa, Arbetsliv och Välfärd</funding><funding>National Institute on Aging</funding><pagination>e12618</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11264110</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(3)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>We sought to characterize cognitive profiles associated with enlarged perivascular spaces (EPVS) among Chinese older adults.&lt;h4>Methods&lt;/h4>This population-based study included 1191 dementia-free participants (age ≥60 years) in the MIND-China MRI Substudy (2018-2020). We visually evaluated EPVS in basal ganglia (BG) and centrum semiovale (CSO), white matter hyperintensities (WMHs), lacunes, cerebral microbleeds (CMBs), and cortical superficial siderosis. We used a neuropsychological test battery to assess cognitive function. Data were analyzed using general linear models.&lt;h4>Results&lt;/h4>Greater BG-EPVS load was associated with lower &lt;i>z&lt;/i>-scores in memory, verbal fluency, and global cognition (&lt;i>p &lt;/i>&lt; 0.05); these associations became non-significant when controlling for other cerebral small vessel disease (CSVD) markers (e.g., WMHs, lacunes, and mixed CMBs). Overall, CSO-EPVS load was not associated with cognitive &lt;i>z&lt;/i>-scores (&lt;i>p &lt;/i>> 0.05); among apolipoprotein E (&lt;i>APOE&lt;/i&gt;) -ε4 carriers, greater CSO-EPVS load was associated with lower verbal fluency &lt;i>z&lt;/i>-score, even when controlling for other CSVD markers (&lt;i>p &lt;/i>&lt; 0.05).&lt;h4>Discussion&lt;/h4>The associations of BG-EPVS with poor cognitive function in older adults are largely attributable to other CSVD markers.&lt;h4>Highlights&lt;/h4>The association of enlarged perivascular spaces (EPVS) with cognitive function in older people is poorly defined.The association of basal ganglia (BG)-EPVS with poor cognition is attributed to other cerebral small vessel disease (CSVD) markers.In apolipoprotein E (&lt;i>APOE&lt;/i>) ε4 carriers, a higher centrum semiovale (CSO)-EPVS load is associated with poorer verbal fluency.</pubmed_abstract><journal>Alzheimer's &amp; dementia (Amsterdam, Netherlands)</journal><pubmed_title>Association of enlarged perivascular spaces with cognitive function in dementia-free older adults: A population-based study.</pubmed_title><pmcid>PMC11264110</pmcid><funding_grant_id>2023‐01125</funding_grant_id><funding_grant_id>2020‐01574</funding_grant_id><funding_grant_id>2017‐05819</funding_grant_id><funding_grant_id>CH2019‐8320</funding_grant_id><funding_grant_id>82001120</funding_grant_id><funding_grant_id>81861138008</funding_grant_id><funding_grant_id>AACSFD‐22‐922844</funding_grant_id><funding_grant_id>2020‐01456</funding_grant_id><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Qiu C</pubmed_authors><pubmed_authors>Hou T</pubmed_authors><pubmed_authors>Han X</pubmed_authors><pubmed_authors>Du Y</pubmed_authors><pubmed_authors>Wardlaw JM</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Song L</pubmed_authors><pubmed_authors>Zhao M</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Wang P</pubmed_authors><pubmed_authors>Cong L</pubmed_authors><pubmed_authors>Launer LJ</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association of enlarged perivascular spaces with cognitive function in dementia-free older adults: A population-based study.</name><description>&lt;h4>Introduction&lt;/h4>We sought to characterize cognitive profiles associated with enlarged perivascular spaces (EPVS) among Chinese older adults.&lt;h4>Methods&lt;/h4>This population-based study included 1191 dementia-free participants (age ≥60 years) in the MIND-China MRI Substudy (2018-2020). We visually evaluated EPVS in basal ganglia (BG) and centrum semiovale (CSO), white matter hyperintensities (WMHs), lacunes, cerebral microbleeds (CMBs), and cortical superficial siderosis. We used a neuropsychological test battery to assess cognitive function. Data were analyzed using general linear models.&lt;h4>Results&lt;/h4>Greater BG-EPVS load was associated with lower &lt;i>z&lt;/i>-scores in memory, verbal fluency, and global cognition (&lt;i>p &lt;/i>&lt; 0.05); these associations became non-significant when controlling for other cerebral small vessel disease (CSVD) markers (e.g., WMHs, lacunes, and mixed CMBs). Overall, CSO-EPVS load was not associated with cognitive &lt;i>z&lt;/i>-scores (&lt;i>p &lt;/i>> 0.05); among apolipoprotein E (&lt;i>APOE&lt;/i&gt;) -ε4 carriers, greater CSO-EPVS load was associated with lower verbal fluency &lt;i>z&lt;/i>-score, even when controlling for other CSVD markers (&lt;i>p &lt;/i>&lt; 0.05).&lt;h4>Discussion&lt;/h4>The associations of BG-EPVS with poor cognitive function in older adults are largely attributable to other CSVD markers.&lt;h4>Highlights&lt;/h4>The association of enlarged perivascular spaces (EPVS) with cognitive function in older people is poorly defined.The association of basal ganglia (BG)-EPVS with poor cognition is attributed to other cerebral small vessel disease (CSVD) markers.In apolipoprotein E (&lt;i>APOE&lt;/i>) ε4 carriers, a higher centrum semiovale (CSO)-EPVS load is associated with poorer verbal fluency.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul-Sep</publication><modification>2025-05-18T13:26:29.633Z</modification><creation>2025-05-18T13:26:29.633Z</creation></dates><accession>S-EPMC11264110</accession><cross_references><pubmed>39045142</pubmed><doi>10.1002/dad2.12618</doi></cross_references></HashMap>