A study published in 2025 shed light on cortical microstructural abnormalities in dementia with Lewy bodies (DLB) and their links to Alzheimer’s disease (AD) copathologies.
DLB, characterized by alpha-synuclein aggregation, often coexists with AD pathologies like beta-amyloid plaques and tau tangles, complicating diagnosis and understanding.
Advanced neuroimaging techniques revealed cortical microstructural abnormalities in DLB patients, impacting cognition and sensorimotor integration.
The study showed that greater AD-related copathology burden exacerbates cortical microstructural disruptions in DLB individuals.
The interplay between alpha-synuclein and AD pathologies may severely impair neuronal functions and disrupt cortical microcircuits in DLB.
Microstructural MRI abnormalities could provide early biomarkers, aiding in early diagnosis and monitoring disease progression in DLB and AD.
Distinct neuritic alterations in DLB patients could enhance differential diagnosis from AD, guiding tailored management strategies more accurately.
The multidisciplinary approach and large cohort in the study strengthen the causal inferences and set a new standard for investigating neurodegenerative diseases.
Longitudinal studies are recommended to track cortical microstructural changes over time and explore biomarkers predictive of disease progression for improved prevention strategies.
The integration of neuroimaging biomarkers with molecular data signifies a shift towards precision neurology, offering insights into dementia heterogeneity and personalized treatment approaches.