<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>35(2)</volume><submitter>Papenberg G</submitter><funding>Alexander von Humboldt Research</funding><funding>Umeå University</funding><funding>Swedish Brain Power</funding><funding>Västerbotten County Council</funding><funding>Innovation Fund of the Max Planck Society</funding><funding>Knut and Alice Wallenberg Foundation</funding><funding>Torsten and Ragnar Söderberg Foundation</funding><funding>Jochnick Foundation</funding><funding>Umeå University-Karolinska Institute Strategic Neuroscience Program</funding><funding>Swedish Brain Foundation</funding><funding>Swedish Research Council</funding><funding>2010 Leibniz Research Award from the German Research Foundation</funding><pubmed_abstract>Although age differences in the dopamine system have been suggested to contribute to age-related cognitive decline based on cross-sectional data, recent large-scale cross-sectional studies reported only weak evidence for a correlation among aging, dopamine receptor availability, and cognition. Regardless, longitudinal data remain essential to make robust statements about dopamine losses as a basis for cognitive aging. We present correlations between changes in D2/3 dopamine receptor availability and changes in working memory measured over 5 yr in healthy, older adults (n = 128, ages 64 to 68 yr at baseline). Greater decline in D2/3 dopamine receptor availability in working memory-relevant regions (caudate, middle frontal cortex, hippocampus) was related to greater decline in working memory</pubmed_abstract><journal>Cerebral cortex (New York, N.Y. : 1991)</journal><pagination>bhae481</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11795306</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Aging-related losses in dopamine D2/3 receptor availability are linked to working-memory decline across five years.</pubmed_title><pmcid>PMC11795306</pmcid><pubmed_authors>Axelsson J</pubmed_authors><pubmed_authors>Nyberg L</pubmed_authors><pubmed_authors>Salami A</pubmed_authors><pubmed_authors>Papenberg G</pubmed_authors><pubmed_authors>Wahlin A</pubmed_authors><pubmed_authors>Lindenberger U</pubmed_authors><pubmed_authors>Backman L</pubmed_authors><pubmed_authors>Karalija N</pubmed_authors><pubmed_authors>Andersson M</pubmed_authors><pubmed_authors>Johansson J</pubmed_authors><pubmed_authors>Garrett DD</pubmed_authors><pubmed_authors>Riklund K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aging-related losses in dopamine D2/3 receptor availability are linked to working-memory decline across five years.</name><description>Although age differences in the dopamine system have been suggested to contribute to age-related cognitive decline based on cross-sectional data, recent large-scale cross-sectional studies reported only weak evidence for a correlation among aging, dopamine receptor availability, and cognition. Regardless, longitudinal data remain essential to make robust statements about dopamine losses as a basis for cognitive aging. We present correlations between changes in D2/3 dopamine receptor availability and changes in working memory measured over 5 yr in healthy, older adults (n = 128, ages 64 to 68 yr at baseline). Greater decline in D2/3 dopamine receptor availability in working memory-relevant regions (caudate, middle frontal cortex, hippocampus) was related to greater decline in working memory</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2025-04-04T07:26:17.727Z</modification><creation>2025-04-04T07:26:17.727Z</creation></dates><accession>S-EPMC11795306</accession><cross_references><pubmed>39756432</pubmed><doi>10.1093/cercor/bhae481</doi></cross_references></HashMap>