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Aβ42 biomarker linked to insula, striatum, thalamus and claustrum in dementia with Lewy bodies.
- Source :
-
GeroScience [Geroscience] 2025 Jan 17. Date of Electronic Publication: 2025 Jan 17. - Publication Year :
- 2025
- Publisher :
- Ahead of Print
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Abstract
- The differential mechanisms between proteinopathies and neurodegeneration in Alzheimer's disease (AD) and dementia with Lewy bodies (DLB) remain unclear. To address this issue, we conducted a voxel-based morphometry and cerebrospinal fluid biomarker (α-synuclein, Aβ42, t-Tau and p-Tau <subscript>181</subscript> ) level correlation study in patients with DLB, AD and mixed cases (AD + DLB). Cerebrospinal fluid samples obtained by lumbar puncture and whole-brain T1-weighted images were collected in the AlphaLewyMA cohort. Within the cohort, 65 DLB patients, 18 AD patients, 24 AD + DLB patients and 16 neurological control subjects (NC) were clinically diagnosed. Correlation analyses were performed between cerebrospinal fluid biomarker levels and gray matter volumes using a voxel-based morphometry approach. A mediation analysis was performed to explore the role of gray matter volumes in the relationship between Aβ42 levels and clinical severity (MMSE scores). We observed a significant positive correlation between gray matter volumes and cerebrospinal fluid Aβ42 levels in the insula, the striatal regions, the right thalamus, and the claustrum in DLB patients (p <subscript>FDR</subscript> < 0.05). Mediation analysis revealed that gray matter volumes significantly mediated the relationship between Aβ42 levels and MMSE scores in DLB patients. We found no significant correlation with gray matter volumes for α-synuclein, p-Tau <subscript>181</subscript> or t-Tau in DLB patients (p <subscript>FDR</subscript> < 0.05). We found no significant correlations in the AD, AD + DLB and NC groups for any of the biomarkers (p <subscript>FDR</subscript> < 0.05). The specific correlation between a reduced cerebrospinal fluid Aβ42 level and lower gray matter volumes in insula, striatum, thalamus, and claustrum in DLB patients suggests a prominent role for amyloidopathy in promoting brain atrophy in key regions of the disease.<br />Competing Interests: Declarations. Ethics approval and consent to participate: This research was approved by the local ethics committee (“Comité de Protection des Personnes Strasbourg Est IV” [CPP-EST-IV]). All participants provided informed consent to participate. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.<br /> (© 2025. The Author(s), under exclusive licence to American Aging Association.)
Details
- Language :
- English
- ISSN :
- 2509-2723
- Database :
- MEDLINE
- Journal :
- GeroScience
- Publication Type :
- Academic Journal
- Accession number :
- 39821801
- Full Text :
- https://doi.org/10.1007/s11357-025-01513-z