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Published on: August 16, 2020
Prodromal clinical manifestations of neuropathologically confirmed Lewy body disease
G A Jicha1, F A Schmitt, E Abner
1Department of Neurology, University of Kentucky College of Medicine, Lexington, KY 40536, USA. gajich2@email.uky.edu
Abstract:
The mild cognitive impairment (MCI) stage of dementia with Lewy bodies (MCI-DLB) has not yet been defined, but is likely to differ in the MCI stage of Alzheimer's disease (MCI-AD). To determine whether clinical features distinguish MCI-DLB and MCI-AD, 9 cases of neuropathologically confirmed MCI-DLB and 12 cases of MCI-AD were compared. No significant differences were found between MCI-DLB and MCI-AD cases in age at death, gender, ApoE status, education, time followed while clinically normal, or duration of MCI. MCI-DLB and MCI-AD cases differed clinically in the expression of Parkinsonism (P=0.012), provoked hallucinations or delirium (P=0.042), or the presence of any of these noncognitive symptoms of DLB (P<0.0001). Letter fluency (P=0.007) was significantly lower and Wechsler Logical Memory I (P=0.019) was significantly higher in MCI-DLB compared to MCI-AD cases. These data demonstrate the feasibility of differentiating underlying pathologic processes responsible for cognitive decline in the preclinical disease state and suggest that further refinement in diagnostic criteria may allow more accurate early detection of prodromal DLB and AD.
Insights
Mild cognitive impairment in dementia with Lewy bodies (MCI-DLB) can be distinguished from Alzheimer
Area of Science:
- Neurology
- Neuroscience
- Pathology
Background:
- The early stages of dementia with Lewy bodies (DLB) and Alzheimer's disease (AD) present diagnostic challenges.
- Mild cognitive impairment (MCI) is a preclinical stage for both neurodegenerative diseases.
- Distinguishing MCI due to DLB (MCI-DLB) from MCI due to AD (MCI-AD) is crucial for timely intervention.
Purpose of the Study:
- To investigate clinical features that differentiate MCI-DLB from MCI-AD.
- To assess the feasibility of early detection of prodromal DLB and AD.
Main Methods:
- Comparison of clinical data from 9 neuropathologically confirmed MCI-DLB cases and 12 MCI-AD cases.
- Analysis of demographic, clinical, and cognitive variables between the two groups.
Main Results:
- No significant differences in age, gender, ApoE status, education, or disease duration were found.
- MCI-DLB cases showed a higher prevalence of Parkinsonism and provoked hallucinations/delirium compared to MCI-AD.
- Letter fluency was lower and logical memory scores were higher in MCI-DLB versus MCI-AD.
Conclusions:
- Clinical features, particularly non-cognitive symptoms, can help distinguish MCI-DLB from MCI-AD.
- These findings support the potential for refining diagnostic criteria for early detection of prodromal DLB and AD.
- Differentiating underlying pathologies in preclinical stages is feasible, aiding in earlier diagnosis and management.
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