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Abstract Details

Vesicular and Immune Dysregulation Identified Through Transcriptomic and Proteomic Profiling in Mixed Dementia with Alzheimer’s and Lewy Body Pathologies
Aging, Dementia, and Behavioral Neurology
S42 - Perspectives on Non-Alzheimer's Dementia Diagnostics and Therapeutics (2:36 PM-2:48 PM)
009

To identify molecular pathways linking vesicular transport and immune dysregulation in brains with mixed Alzheimer’s disease pathology (ADP) and Lewy-related pathology (LRP).

Mixed dementia involving ADP and LRP is common but remains poorly understood at the molecular level. Dysregulation of vesicular transport and immune signaling may underlie the convergence of these disease processes.

RNA sequencing and proteomic profiling were performed on brain tissue from medial frontal gyrus (MFG), superior temporal gyrus (STG), and cerebrospinal fluid (CSF) from a cohort of 92 subjects, including those with Alzheimer's disease (AD, n=23), Lewy body dementia (LBD, n=23), mixed AD/LBD (n=26), and controls (n=20).  Differential expression, principal component, and pathway enrichment analyses identified shared and distinct molecular signatures across disease groups.

 

Transcriptomic analysis revealed distinct gene expression patterns for each pathology, with mixed cases showing overlapping activation of immune, vesicle trafficking, and chromatin remodeling pathways.  In the STG, the strongest protein-level differences were related to synaptic organization and vesicular transport. Integrative network analyses highlighted coordinated dysregulation of immune and vesicle-associated processes across modalities.

Combined transcriptomic and proteomic evidence suggests that interplay between vesicular transport and immune-related pathways contributes to mixed Alzheimer’s–Lewy body pathology. These findings provide a molecular framework for biomarker development and therapeutic exploration in mixed dementias.

Authors/Disclosures
Gurkan Bebek, PhD
PRESENTER
Dr. Bebek has nothing to disclose.
Hyun Jo Kim (Case Western Reserve University) No disclosure on file
Spancer Zhou, MD Miss Zhou has nothing to disclose.
Dirk Keene, MD, PhD Dirk Keene, MD, PhD has received publishing royalties from a publication relating to health care.
James B. Leverenz, MD, FAAN (Cleveland Clinic) Dr. Leverenz has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Acadia. Dr. Leverenz has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Biogen. Dr. Leverenz has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Eisai.
Jagan Pillai, MD, PhD, FAAN (Cleveland Clinic) Dr. Pillai has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Springer Nature. Dr. Pillai has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Current Treatment Options in Neurology. The institution of Dr. Pillai has received research support from Alzheimer's Association. The institution of Dr. Pillai has received research support from Keep Memory Alive Foundation . The institution of Dr. Pillai has received research support from NIA. Dr. Pillai has received personal compensation in the range of $500-$4,999 for serving as a Reviewer with DOD. Dr. Pillai has received personal compensation in the range of $500-$4,999 for serving as a Reviewer with RGC Hong kong.