{"title":"2型糖尿病和阿尔茨海默病皮质神经变性的共性","authors":"Mahboubeh Motaghi, Olivier Potvin, Simon Duchesne","doi":"10.1177/13872877251365671","DOIUrl":null,"url":null,"abstract":"<p><p>BackgroundType 2 diabetes (T2D) is a prevalent metabolic condition associated with increased risk of cognitive decline and dementia, including Alzheimer's disease (AD). While both T2D and AD are linked to neurodegeneration, the extent to which their patterns of brain atrophy overlap remain unclear.ObjectiveTo assess the similarities and differences in cortical atrophy patterns among individuals with controlled and uncontrolled T2D, mild cognitive impairment (MCI), and AD.MethodsStructural magnetic resonance imaging data from the UK Biobank (UKBB) and the Alzheimer's Disease Neuroimaging Initiative (ADNI) were analyzed. Participants aged 55 and older were selected. Linear regression models were applied to generate cortical thickness maps for each group, controlling for age and sex. Group comparisons were conducted using permutation-based tests accounting for spatial autocorrelation.ResultsThe study included 175 individuals with T2D (86 uncontrolled, 89 controlled) and 127 healthy controls without diabetes (HC) from UKBB, 334 individuals with MCI, 119 with AD and 315 cognitively healthy (CH) from ADNI. Uncontrolled T2D was associated with significant cortical atrophy in specific brain regions, with partial overlap in neurodegeneration patterns observed in MCI and AD. However, correlations between the cortical thinning patterns were weak and non-significant, suggesting distinct trajectories. Controlled T2D showed no significant cortical thinning, supporting the potential neuroprotective effects of glycemic control.ConclusionsUncontrolled T2D is linked to region-specific cortical atrophy that partially overlaps with MCI and AD but follows an independent neurodegenerative trajectory. Effective diabetes management may help preserve brain structure and reduce dementia risk, highlighting the importance of early metabolic intervention.</p>","PeriodicalId":14929,"journal":{"name":"Journal of Alzheimer's Disease","volume":" ","pages":"1304-1318"},"PeriodicalIF":3.1000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12449609/pdf/","citationCount":"0","resultStr":"{\"title\":\"Commonalities in cortical neurodegeneration between type 2 diabetes and Alzheimer's disease.\",\"authors\":\"Mahboubeh Motaghi, Olivier Potvin, Simon Duchesne\",\"doi\":\"10.1177/13872877251365671\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>BackgroundType 2 diabetes (T2D) is a prevalent metabolic condition associated with increased risk of cognitive decline and dementia, including Alzheimer's disease (AD). While both T2D and AD are linked to neurodegeneration, the extent to which their patterns of brain atrophy overlap remain unclear.ObjectiveTo assess the similarities and differences in cortical atrophy patterns among individuals with controlled and uncontrolled T2D, mild cognitive impairment (MCI), and AD.MethodsStructural magnetic resonance imaging data from the UK Biobank (UKBB) and the Alzheimer's Disease Neuroimaging Initiative (ADNI) were analyzed. Participants aged 55 and older were selected. Linear regression models were applied to generate cortical thickness maps for each group, controlling for age and sex. Group comparisons were conducted using permutation-based tests accounting for spatial autocorrelation.ResultsThe study included 175 individuals with T2D (86 uncontrolled, 89 controlled) and 127 healthy controls without diabetes (HC) from UKBB, 334 individuals with MCI, 119 with AD and 315 cognitively healthy (CH) from ADNI. Uncontrolled T2D was associated with significant cortical atrophy in specific brain regions, with partial overlap in neurodegeneration patterns observed in MCI and AD. However, correlations between the cortical thinning patterns were weak and non-significant, suggesting distinct trajectories. Controlled T2D showed no significant cortical thinning, supporting the potential neuroprotective effects of glycemic control.ConclusionsUncontrolled T2D is linked to region-specific cortical atrophy that partially overlaps with MCI and AD but follows an independent neurodegenerative trajectory. Effective diabetes management may help preserve brain structure and reduce dementia risk, highlighting the importance of early metabolic intervention.</p>\",\"PeriodicalId\":14929,\"journal\":{\"name\":\"Journal of Alzheimer's Disease\",\"volume\":\" \",\"pages\":\"1304-1318\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12449609/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Alzheimer's Disease\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1177/13872877251365671\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/10 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alzheimer's Disease","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/13872877251365671","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/10 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
Commonalities in cortical neurodegeneration between type 2 diabetes and Alzheimer's disease.
BackgroundType 2 diabetes (T2D) is a prevalent metabolic condition associated with increased risk of cognitive decline and dementia, including Alzheimer's disease (AD). While both T2D and AD are linked to neurodegeneration, the extent to which their patterns of brain atrophy overlap remain unclear.ObjectiveTo assess the similarities and differences in cortical atrophy patterns among individuals with controlled and uncontrolled T2D, mild cognitive impairment (MCI), and AD.MethodsStructural magnetic resonance imaging data from the UK Biobank (UKBB) and the Alzheimer's Disease Neuroimaging Initiative (ADNI) were analyzed. Participants aged 55 and older were selected. Linear regression models were applied to generate cortical thickness maps for each group, controlling for age and sex. Group comparisons were conducted using permutation-based tests accounting for spatial autocorrelation.ResultsThe study included 175 individuals with T2D (86 uncontrolled, 89 controlled) and 127 healthy controls without diabetes (HC) from UKBB, 334 individuals with MCI, 119 with AD and 315 cognitively healthy (CH) from ADNI. Uncontrolled T2D was associated with significant cortical atrophy in specific brain regions, with partial overlap in neurodegeneration patterns observed in MCI and AD. However, correlations between the cortical thinning patterns were weak and non-significant, suggesting distinct trajectories. Controlled T2D showed no significant cortical thinning, supporting the potential neuroprotective effects of glycemic control.ConclusionsUncontrolled T2D is linked to region-specific cortical atrophy that partially overlaps with MCI and AD but follows an independent neurodegenerative trajectory. Effective diabetes management may help preserve brain structure and reduce dementia risk, highlighting the importance of early metabolic intervention.
期刊介绍:
The Journal of Alzheimer''s Disease (JAD) is an international multidisciplinary journal to facilitate progress in understanding the etiology, pathogenesis, epidemiology, genetics, behavior, treatment and psychology of Alzheimer''s disease. The journal publishes research reports, reviews, short communications, hypotheses, ethics reviews, book reviews, and letters-to-the-editor. The journal is dedicated to providing an open forum for original research that will expedite our fundamental understanding of Alzheimer''s disease.