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Published on: November 8, 2024
Inflammation in dementia with Lewy bodies
Jay Amin1, Daniel Erskine2, Paul C Donaghy2
1Clinical Neurosciences, Clinical and Experimental Sciences, Faculty of Medicine, University of Southampton, UK; Memory Assessment and Research Centre, Southern Health NHS Foundation Trust, Southampton, UK..
Inflammation may be elevated in early Dementia with Lewy bodies (DLB), potentially driven by alpha-synuclein and Alzheimer's co-pathology. This neuroinflammation appears to decrease as the disease progresses.
Area of Science:
- Neuroscience
- Immunology
- Pathology
Background:
- Dementia with Lewy bodies (DLB) is the second most common neurodegenerative dementia after Alzheimer's disease (AD).
- While inflammation in AD is well-studied, its role in DLB pathogenesis is less understood.
- Existing research often focuses on related disorders like Parkinson's disease.
Purpose of the Study:
- To review and synthesize current literature on the role of neuroinflammation in Dementia with Lewy bodies.
- To explore various methodologies used to study inflammation in DLB.
- To identify potential diagnostic markers and therapeutic targets related to inflammation in DLB.
Main Methods:
- Literature review encompassing cerebrospinal fluid, peripheral blood, post-mortem brain tissue analysis, neuroimaging (PET), and preclinical studies.
- Quantification of inflammatory markers across different disease stages.
- Examination of the influence of alpha-synuclein and AD co-pathology on neuroinflammation.
Main Results:
- Evidence suggests increased cerebral and peripheral inflammation in mild/prodromal DLB, which diminishes with disease progression.
- Alpha-synuclein appears to directly promote inflammation.
- Alzheimer's disease co-pathology significantly influences the neuroinflammatory profile in DLB.
Conclusions:
- Inflammation may serve as a sentinel marker in early DLB, especially with co-existing AD pathology.
- Further longitudinal studies are crucial for understanding DLB pathogenesis.
- Identifying inflammatory profiles could lead to diagnostic biomarkers and novel therapeutic strategies for DLB.
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