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BackgroundAlzheimer's disease (AD) is a progressive neurodegenerative disorder with extensive neuropathological and clinical heterogeneity.ObjectiveWe assessed empirically derived brain atrophy profiles in relation to incident AD dementia.MethodsA secondary data analysis of two prospective cohort studies was conducted, including participants without dementia from the Alzheimer's Disease Neuroimaging Initiative (ADNI; = 1703) and the Czech Brain Aging Study (CBAS; = 385). Latent profile analysis identified profiles across 10 pre-selected, AD-related brain regions derived from structural magnetic resonance imaging (hippocampus, middle temporal, superior temporal, precuneus, anterior cingulate, medial orbitofrontal, pericalcarine, precentral, lingual, caudate regions). Cox proportional hazards regression assessed how profiles related to incident AD dementia.ResultsFour profiles emerged in ADNI: Minimal ( = 192), Mild ( = 691), Moderate ( = 567), and Severe ( = 253) Atrophy. Two profiles emerged in CBAS: Mild ( = 208) and Severe ( = 177) Atrophy. In ADNI, participants with Mild (HR = 3.11, 95% CI [1.43, 6.78]), Moderate (HR = 7.58, 95% CI [3.45, 16.68]), and Severe (HR = 16.95, 95% CI [7.39, 39.86]) Atrophy (versus Minimal) had increased incident AD dementia risk. In CBAS, participants with Severe Atrophy (versus Mild) had increased incident AD dementia risk (HR = 3.51, 95% CI [2.14, 5.77]). Controlling for baseline cognition attenuated effects for Mild (ADNI) and Severe (CBAS) Atrophy to non-significance.ConclusionsIn two geographically and culturally distinct samples, magnitude of atrophy, not pattern across regions, determined classification into profiles, which predicted incident AD dementia. Findings highlight generalized, rather than region-specific, atrophy patterns associated with AD, and underscore the clinical utility of brain volumetry in identifying those with elevated incident AD dementia risk.
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http://dx.doi.org/10.1177/13872877251371734 | DOI Listing |
Mol Nutr Food Res
September 2025
Department of Epidemiology and Health Statistics, School of Public Health, Qingdao University, Qingdao, China.
The relationship between dietary biotin intake and cognitive function remains unclear. This study explores the association between biotin and dementia, and the mediating role of inflammation indicators. Dietary biotin intake was assessed via the 24-h recall questionnaire.
View Article and Find Full Text PDFCell Rep
September 2025
Feil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, NY, USA; Center for Neurogenetics, Weill Cornell Medicine, New York, NY, USA. Electronic address:
Progranulin-deficient frontotemporal dementia (GRN-FTD) is a major cause of familial FTD with TAR DNA-binding protein 43 (TDP-43) pathology, which is linked to exon dysregulation. However, little is known about this dysregulation in glial and neuronal cells. Here, using splice-junction-covering enrichment probes, we introduce single-nuclei long-read RNA sequencing 2 (SnISOr-Seq2), targeting 3,630 high-interest genes without loss of precision, and complete the first single-cell, long-read-resolved case-control study for neurodegeneration.
View Article and Find Full Text PDFJAMA Netw Open
September 2025
Department of Neurosciences, University of California, San Diego, La Jolla.
Importance: Subjective cognitive decline (SCD) may be an early indicator of Alzheimer disease and related dementias (ADRD), yet its association with plasma biomarkers remains unclear among middle-aged and older adults (aged 50-86 years).
Objective: To examine associations between plasma biomarkers of amyloid, tau, neuroaxonal damage, and glial activation with SCD in a heterogeneous cohort of Hispanic and/or Latino adults.
Design, Setting, And Participants: This cross-sectional study used survey-weighted data from the Study of Latinos-Investigation of Neurocognitive Aging, an ancillary study of the Hispanic Community Health Study/Study of Latinos.
Geroscience
September 2025
Department of Epidemiology, School of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
Introduction: Cancer is associated with accelerated aging, including changes in muscle composition and cognition. However, the relationship between myosteatosis and cognitive function has not been investigated in older cancer survivors. This study evaluated the association between myosteatosis and cognitive function in this population.
View Article and Find Full Text PDFJ Neurol
September 2025
Department of Neurology & Innovation Center for Neurological Disorders, National Center for Neurological Disorders, Xuanwu Hospital, Capital Medical University, No. 45 Changchun Street, Beijing, 100053, China.
Background: Sleep deprivation has been linked to higher dementia risk, but the role of weekend recovery sleep (WRS) in mitigating this risk remains unclear. This study aims to evaluate the association between WRS and dementia risk.
Methods: This prospective cohort study followed 88,592 dementia-free adults aged 40-79 years from the UK Biobank, using wrist accelerometers to measure average weekday and weekend sleep durations.