<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Machulda MM</submitter><funding>NIA NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>1013-1022</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7383989</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(7)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>We examined differences in cortical thickness in empirically derived mild cognitive impairment (MCI) subtypes in the Mayo Clinic Study of Aging.&lt;h4>Methods&lt;/h4>We compared cortical thickness of four incident MCI subtypes (n = 192) to 1257 cognitive unimpaired individuals.&lt;h4>Results&lt;/h4>The subtle cognitive impairment cluster had atrophy in the entorhinal and parahippocampal cortex. The amnestic, dysnomic, and dysexecutive clusters also demonstrated entorhinal cortex atrophy as well as thinning in temporal, parietal, and frontal isocortex in somewhat different patterns.&lt;h4>Discussion&lt;/h4>We found patterns of atrophy in each of the incident MCI clusters that corresponded to their patterns of cognitive impairment. The identification of MCI subtypes based on cognitive and</pubmed_abstract><journal>Alzheimer's &amp; dementia : the journal of the Alzheimer's Association</journal><pubmed_title>Cortical atrophy patterns of incident MCI subtypes in the Mayo Clinic Study of Aging.</pubmed_title><pmcid>PMC7383989</pmcid><funding_grant_id>R37 AG011378</funding_grant_id><funding_grant_id>U01 AG06786</funding_grant_id><funding_grant_id>R01 AG041851</funding_grant_id><funding_grant_id>P50 AG016574</funding_grant_id><funding_grant_id>R01 AG49810</funding_grant_id><funding_grant_id>U01 AG006786</funding_grant_id><funding_grant_id>R01 AG011378</funding_grant_id><funding_grant_id>R01 AG034676</funding_grant_id><funding_grant_id>R01 AG056366</funding_grant_id><funding_grant_id>R01 AG049810</funding_grant_id><funding_grant_id>P30 AG062429</funding_grant_id><funding_grant_id>R01 NS097495</funding_grant_id><pubmed_authors>Albertson SM</pubmed_authors><pubmed_authors>Mielke MM</pubmed_authors><pubmed_authors>Bondi MW</pubmed_authors><pubmed_authors>Lundt ES</pubmed_authors><pubmed_authors>Jack CR</pubmed_authors><pubmed_authors>Knopman DS</pubmed_authors><pubmed_authors>Kremers WK</pubmed_authors><pubmed_authors>Petersen RC</pubmed_authors><pubmed_authors>Schwarz CG</pubmed_authors><pubmed_authors>Machulda MM</pubmed_authors><pubmed_authors>Jones DT</pubmed_authors><pubmed_authors>Spychalla AJ</pubmed_authors><pubmed_authors>Vemuri P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cortical atrophy patterns of incident MCI subtypes in the Mayo Clinic Study of Aging.</name><description>&lt;h4>Introduction&lt;/h4>We examined differences in cortical thickness in empirically derived mild cognitive impairment (MCI) subtypes in the Mayo Clinic Study of Aging.&lt;h4>Methods&lt;/h4>We compared cortical thickness of four incident MCI subtypes (n = 192) to 1257 cognitive unimpaired individuals.&lt;h4>Results&lt;/h4>The subtle cognitive impairment cluster had atrophy in the entorhinal and parahippocampal cortex. The amnestic, dysnomic, and dysexecutive clusters also demonstrated entorhinal cortex atrophy as well as thinning in temporal, parietal, and frontal isocortex in somewhat different patterns.&lt;h4>Discussion&lt;/h4>We found patterns of atrophy in each of the incident MCI clusters that corresponded to their patterns of cognitive impairment. The identification of MCI subtypes based on cognitive and</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2025-04-19T23:01:03.532Z</modification><creation>2025-04-19T23:01:03.532Z</creation></dates><accession>S-EPMC7383989</accession><cross_references><pubmed>32418367</pubmed><doi>10.1002/alz.12108</doi></cross_references></HashMap>