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We investigated OGTT and other glycaemia and insulin resistance markers, and cognitive and neuroimaging changes in the Finnish Geriatric Intervention Study to Prevent Cognitive Impairment and Disability (FINGER).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Materials and Methods<\/jats:title>\n                    <jats:p>\n                      At\u2010risk individuals aged 60\u201377\u00a0years without dementia (\n                      <jats:italic>N<\/jats:italic>\n                      \u00a0=\u00a01259) were randomly enrolled in a 2\u2010year multidomain lifestyle intervention or regular health advice program. 1025 participants without previously diagnosed diabetes underwent OGTT. Brain MRI scans were available for 132 participants and amyloid (PiB)\u2010PET and FDG\u2010PET scans for 47. Cognition was assessed using the modified Neuropsychological Test Battery (mNTB).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Higher baseline dysglycaemia measures, particularly those from the OGTT, were connected to less favourable changes in multiple cognitive measures and hippocampal volume. Higher baseline triglyceride\u2010glucose (TyG) index was associated with higher amyloid accumulation and decline in brain glucose metabolism. Higher baseline glycated haemoglobin (HbA1c) was related to favourable changes in processing speed and cortical thickness. There were no significant intervention\u2010control differences in the change in glycaemia markers. Baseline dysglycaemia and glycaemia\u2010related markers did not modify the previously reported intervention benefits on cognition.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Higher baseline dysglycaemia measures are linked to more deleterious changes in cognition. Specifically, OGTT measures may be the most sensitive for detecting subtle glycaemic abnormalities associated with both unfavourable cognitive and neuroimaging changes. However, HbA1c shows mixed associations with cognition and neuroimaging in people at risk of dementia without previously diagnosed diabetes. This study emphasises the importance of more accurate glucose\u2010related markers when investigating early stages of glucose metabolism abnormalities and their relationship to subtle cognitive impairment and its structural brain correlates.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Trial Registration<\/jats:title>\n                    <jats:p>\n                      ID NCT01041989\n                      <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/clinicaltrials.gov\/\">https:\/\/clinicaltrials.gov<\/jats:ext-link>\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/dmrr.70053","type":"journal-article","created":{"date-parts":[[2025,6,6]],"date-time":"2025-06-06T12:04:41Z","timestamp":1749211481000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":8,"title":["Associations of Prediabetes, Diabetes and Glucose\u2010Related Markers With Cognition and Neuroimaging in a 2\u2010Year Multidomain Lifestyle Randomised Controlled Trial"],"prefix":"10.1002","volume":"41","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7664-8693","authenticated-orcid":false,"given":"Thais","family":"Lorenzo","sequence":"first","affiliation":[{"name":"Neuroimaging Research Group BarcelonaBeta Brain Research Centre  Barcelona Spain"},{"name":"Division of Clinical Geriatrics Center for Alzheimer Research NVS Karolinska Institutet  Stockholm Sweden"},{"name":"Neuroimaging of neurodegenerative Diseases and Healthy Aging Neuroscience Research Program Hospital Del Mar Research Institute  Barcelona Spain"},{"name":"Department of Medicine and Life Sciences Universitat Pompeu Fabra  Barcelona Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tiia","family":"Ngandu","sequence":"additional","affiliation":[{"name":"Division of Clinical Geriatrics Center for Alzheimer Research NVS 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