Ontology highlight
ABSTRACT: Background
Late-onset Alzheimer's disease (LOAD) has been associated with alterations in the morphology of multiple brain structures, and it is likely that disease mechanisms differ between brain regions. Coupling genetic determinants of LOAD with measures of brain morphology could localize and identify primary causal neurobiological pathways.Objective
To determine causal pathways from genetic risk variants of LOAD via brain morphology to LOAD.Methods
Mediation and Mendelian randomization (MR) analysis were performed using common genetic variation, T1 MRI and clinical data collected by UK Biobank and Alzheimer's Disease Neuroimaging Initiative.Results
Thickness of the entorhinal cortex and the volumes of the hippocampus, amygdala and inferior lateral ventric
SUBMITTER: Breddels EM
PROVIDER: S-EPMC11938454 | biostudies-literature | 2025 Jan-Dec
REPOSITORIES: biostudies-literature