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Comorbid Pathologies and Their Impact on Dementia with Lewy Bodies-Current View
1Institute of Clinical Neurobiology, 1150 Vienna, Austria.
Dementia with Lewy bodies (DLB) often co-occurs with other brain conditions and disorders. Identifying these co-pathologies with biomarkers is crucial for accurate diagnosis and predicting DLB progression.
Area of Science:
- Neurology
- Neuroscience
- Pathology
Background:
- Dementia with Lewy bodies (DLB) is a primary neurocognitive disorder, second to Alzheimer disease (AD).
- DLB frequently exhibits co-pathologies, including Alzheimer disease-related neuropathological changes (ADNC), TDP-43 proteinopathies, and cardiovascular/aging disorders.
- Cerebrovascular lesions and cardiovascular conditions like hypertension and hyperlipidemia are common comorbidities in DLB.
Purpose of the Study:
- To review the types and frequency of co-pathologies in DLB.
- To assess the clinical impact of these co-pathologies on DLB patients.
- To evaluate the utility of biomarkers for assessing and preventing DLB and its co-pathologies.
Main Methods:
- Literature review of neuropathological and clinical studies on DLB co-pathologies.
- Analysis of the prevalence and impact of co-existing conditions in DLB.
- Evaluation of biomarker potential for DLB diagnosis and progression prediction.
Main Results:
- Alzheimer disease-related neuropathological changes (ADNC) and TDP-43 proteinopathies are common co-pathologies in DLB.
- Cerebrovascular lesions, particularly cerebral amyloid angiopathy, are the most frequent non-neurodegenerative co-pathologies.
- Cardiovascular disorders, hypertension, and hyperlipidemia are highly prevalent comorbidities in DLB patients.
Conclusions:
- Co-pathologies significantly influence DLB clinical presentation and progression.
- Clinical trial designs for DLB should incorporate the impact of co-pathologies.
- Biomarker evaluation for co-pathologies can enhance diagnostic accuracy and predict clinical outcomes in DLB.
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