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Tau in dementia with Lewy bodies
Kai Sin Chin1,2,3, Leonid Churilov4, Vincent Doré5,6
1Department of Medicine, The Royal Melbourne Hospital, The University of Melbourne, Parkville, VIC, Australia.
Plasma p-tau181 shows promise as a biomarker for detecting co-occurring Alzheimer's disease pathology in dementia with Lewy bodies. This blood test correlates with abnormal tau and amyloid PET scans, aiding in identifying mixed pathologies.
Area of Science:
- Neurology
- Neuroimaging
- Biomarker Discovery
Background:
- Neurofibrillary tangles, a hallmark of Alzheimer's disease, are found in some dementia with Lewy bodies (DLB) cases and may worsen cognitive decline.
- Advances in Alzheimer's disease biomarkers include second-generation tau positron emission tomography (PET) and plasma detection of phosphorylated tau at threonine 181 (p-tau181).
Purpose of the Study:
- To investigate the presence and implications of tau pathology in individuals with dementia with Lewy bodies.
- To evaluate the utility of second-generation tau PET imaging and plasma p-tau181 as biomarkers in DLB.
Main Methods:
- Twenty-seven participants with probable DLB underwent PET imaging using 18F-MK6240 and 18F-NAV4694 tracers.
- Plasma p-tau181 levels were quantified using Simoa technology.
Main Results:
- 18.5% of DLB participants exhibited abnormal tau PET scans.
- Plasma p-tau181 concentrations positively correlated with temporal tau deposition (ρ = 0.46) and predicted abnormal tau PET.
- Plasma p-tau181 also correlated with amyloid-beta PET binding (ρ = 0.68) and predicted abnormal amyloid-beta PET.
Conclusions:
- Tau pathology is a frequent co-occurring condition in dementia with Lewy bodies.
- Plasma p-tau181 may serve as a valuable blood-based marker for identifying comorbid Alzheimer's disease-related pathologies in DLB.
- Further large-scale longitudinal studies are required to elucidate the clinical significance of tau in DLB.
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