<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pink A</submitter><funding>GHR Foundation</funding><funding>Alexander Family Alzheimer's Disease Research Professorship of the Mayo Clinic</funding><funding>Schuler Foundation</funding><funding>Mayo Foundation for Medical Education and Research</funding><funding>Arizona Alzheimer&amp;apos;s Consortium</funding><funding>NIA NIH HHS</funding><funding>Arizona Alzheimers Consortium</funding><funding>Schuler-Stiftung</funding><funding>Liston Award</funding><funding>Barrow Neurological Foundation</funding><funding>National Institute on Aging</funding><funding>Robert H. and Clarice Smith and Abigail Van Buren Alzheimers Disease Research Program</funding><pagination>345-354</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12931372</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>74(2)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Previous studies on the relationship between prediabetes, HbA1c and cognitive trajectories show mixed results. Therefore, we investigated the association of prediabetes, diabetes and HbA1c with change in global and domain-specific cognitive scores in cognitively unimpaired (CU) adults, as well as the potential effect modification by sex or age.&lt;h4>Methods&lt;/h4>This longitudinal study included 4236 CU persons aged ≥ 50 years from the population-based Mayo Clinic Study of Aging. We ran linear mixed-effect models with baseline prediabetes, diabetes and HbA1c predicting longitudinal global and domain-specific (i.e., memory, language, attention/executive function, and visuospatial skills) cognitive z-scores and raw scores. Models were adjusted for age, sex, education, medical </pubmed_abstract><journal>Journal of the American Geriatrics Society</journal><pubmed_title>A Longitudinal Investigation of Prediabetes, Diabetes, HbA1c and Cognitive Trajectories Among Cognitively Unimpaired Individuals.</pubmed_title><pmcid>PMC12931372</pmcid><funding_grant_id>R37 AG011378</funding_grant_id><funding_grant_id>R01 AG041851</funding_grant_id><funding_grant_id>P30 AG062677</funding_grant_id><funding_grant_id>U01 AG006786</funding_grant_id><funding_grant_id>R01 AG057708</funding_grant_id><funding_grant_id>R01 NS097495</funding_grant_id><pubmed_authors>Geda YE</pubmed_authors><pubmed_authors>Krell-Roesch J</pubmed_authors><pubmed_authors>Vassilaki M</pubmed_authors><pubmed_authors>Syrjanen JA</pubmed_authors><pubmed_authors>Fields JA</pubmed_authors><pubmed_authors>Jack CR</pubmed_authors><pubmed_authors>Pink A</pubmed_authors><pubmed_authors>Aigner E</pubmed_authors><pubmed_authors>Racette SB</pubmed_authors><pubmed_authors>Iglseder B</pubmed_authors><pubmed_authors>Kremers WK</pubmed_authors><pubmed_authors>Petersen RC</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Longitudinal Investigation of Prediabetes, Diabetes, HbA1c and Cognitive Trajectories Among Cognitively Unimpaired Individuals.</name><description>&lt;h4>Background&lt;/h4>Previous studies on the relationship between prediabetes, HbA1c and cognitive trajectories show mixed results. Therefore, we investigated the association of prediabetes, diabetes and HbA1c with change in global and domain-specific cognitive scores in cognitively unimpaired (CU) adults, as well as the potential effect modification by sex or age.&lt;h4>Methods&lt;/h4>This longitudinal study included 4236 CU persons aged ≥ 50 years from the population-based Mayo Clinic Study of Aging. We ran linear mixed-effect models with baseline prediabetes, diabetes and HbA1c predicting longitudinal global and domain-specific (i.e., memory, language, attention/executive function, and visuospatial skills) cognitive z-scores and raw scores. Models were adjusted for age, sex, education, medical </description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-09T12:24:11.215Z</modification><creation>2026-07-09T11:17:46.415Z</creation></dates><accession>S-EPMC12931372</accession><cross_references><pubmed>41348388</pubmed><doi>10.1111/jgs.70231</doi></cross_references></HashMap>