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False Memory and Alzheimer's Disease Pathology in Patients with Amnestic Mild Cognitive Impairment: A Study with
Eun-Ji Choi1, Bum Joon Kim1, Hyung-Ji Kim1
1Department of Neurology, Asan Medical Center, Seoul, Republic of Korea.
Introduction:
False memory, observed as intrusion errors or false positives (FPs), is prevalent in patients with Alzheimer's disease, but has yet to be thoroughly investigated in patients with amnestic mild cognitive impairment (a-MCI) with Alzheimer's disease pathology (ADP). We analyzed false versus veridical memory in individuals with a-MCI and measured the utility of false memory for ADP discrimination.
Methods:
Patients with a-MCI who received neuropsychological testing and amyloid PET were included. Patients were categorized into "with" and "without ADP" groups according to PET results. Memory tests assessed veridical and false memory, and the verity of patient responses was analyzed. A logistic regression model was used to evaluate false memory efficiency in discriminating ADP, and the sensitivity and specificity at the optimal level were estimated using the receiver-operating characteristic curve.
Results:
Thirty-seven ADP and 46 non-ADP patients were enrolled. The ADP group made more FPs in the recognition tests, and their response verity was significantly lower in every delayed memory test. No group difference, however, was observed in the veridical memory. The logistic regression analysis demonstrated that as the FPs increased, the risk of ADP increased 1.31 and 1.36 times in the verbal and visual recognition tests, respectively. The discriminatory accuracy of the FPs was estimated "low" to "moderate" in the visual and verbal recognition, respectively, with an optimal cutoff above 2.5.
Conclusion:
Increased false memory was the only feature to discriminate ADP from non-ADP in individuals with a-MCI. Further studies regarding false memory and its mechanism are warranted.
Insights
Increased false memory, or false positives (FPs), helps identify Alzheimer's disease pathology (ADP) in individuals with amnestic mild cognitive impairment (a-MCI). This finding highlights the diagnostic potential of memory errors in early Alzheimer's detection.
Area of Science:
- Neuroscience
- Cognitive Psychology
- Medical Diagnostics
Background:
- False memory, characterized by intrusion errors or false positives (FPs), is common in Alzheimer's disease (AD).
- Investigation into FPs in amnestic mild cognitive impairment (a-MCI) with Alzheimer's disease pathology (ADP) is limited.
- This study examines false versus veridical memory in a-MCI patients to assess FP utility for ADP discrimination.
Purpose of the Study:
- To analyze false and true memory performance in individuals with a-MCI.
- To determine if false memory can effectively discriminate between a-MCI patients with and without Alzheimer's disease pathology (ADP).
- To evaluate the diagnostic accuracy of false memory for identifying ADP.
Main Methods:
- Patients with a-MCI were assessed using neuropsychological testing and amyloid PET scans to categorize them into "with ADP" and "without ADP" groups.
- Memory tests were administered to evaluate both veridical (true) and false memory recall.
- Logistic regression and receiver-operating characteristic (ROC) curve analysis were employed to assess the discriminatory power of false memory for ADP.
Main Results:
- The group with ADP exhibited significantly more FPs and lower response verity across delayed memory tests compared to the non-ADP group.
- No significant differences in veridical memory performance were found between the groups.
- Increased FPs were associated with a 1.31-1.36 times higher risk of ADP, with low to moderate discriminatory accuracy.
Conclusions:
- Elevated false memory, specifically FPs, emerged as a key indicator for differentiating ADP from non-ADP in a-MCI patients.
- Further research into the mechanisms of false memory is crucial for understanding its role in Alzheimer's disease progression.
- False memory performance shows potential as a biomarker for early Alzheimer's detection in a-MCI.
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