The Role of MRI Biomarkers and Their Interactions with Cognitive Status and APOE ε4 in Nondemented Elderly Subjects
Xue Liang1, Zhenyu Yin2, Renyuan Liu3
1Department of Radiology, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China.
Purpose:
(1) To investigate atrophy patterns of hippocampal subfield volume and Alzheimer's disease (AD)-signature cortical thickness in mild cognitive impairment (MCI) patients; (2) to explore the association between the neuropsychological (NP) and the brain structure in the MCI and older normal cognition group; (3) to determine whether these associations were modified by the apolipoprotein E (APOE) ε4 gene and cognitive status.
Methods:
The FreeSurfer software was used for automated segmentation of hippocampal subfields and AD-signature cortical thickness for 22 MCI patients and 23 cognitive normal controls (NC). The volume, cortical thickness, and the neuropsychological scale were compared with two-sample t tests. Linear regression models were used to determine the association between the NP and the brain structure.
Results:
Compared with the NC group, MCI patients showed a decreased volume of the left presubiculum, subiculum and right CA2_3 and CA4_DG (p < 0.05, FDR corrected). The volume of these regions was positively correlated with NP scores. Of note, these associations depended on the cognitive status but not on the APOE ε4 status. The left subiculum and presubiculum volume were positively correlated with the Montreal Cognitive Assessment (MoCA) scores only in the MCI patients.
Conclusion:
Atrophy of the hippocampal subfields may be a powerful biomarker for MCI in the Chinese population.
Insights
Hippocampal subfield atrophy is a key indicator in mild cognitive impairment (MCI) patients. These brain structure changes correlate with cognitive function, particularly in MCI individuals, suggesting potential as a biomarker.
Area of Science:
- Neuroimaging
- Neuropsychology
- Genetics
Background:
- Mild cognitive impairment (MCI) represents a transitional stage between normal aging and Alzheimer's disease (AD).
- Understanding brain structure changes and their relationship with cognitive function in MCI is crucial for early diagnosis and intervention.
- The role of apolipoprotein E (APOE) ε4 genotype in modulating these relationships requires further investigation.
Purpose of the Study:
- To identify specific patterns of hippocampal subfield and cortical thickness atrophy in MCI patients.
- To investigate the association between neuropsychological (NP) performance and brain structure in MCI and normal cognition (NC) groups.
- To determine if APOE ε4 status and cognitive status modify the relationship between brain structure and NP measures.
Main Methods:
- Automated segmentation of hippocampal subfields and AD-signature cortical thickness using FreeSurfer software.
- Comparison of brain structure volumes and cortical thickness between 22 MCI patients and 23 NC individuals.
- Statistical analysis including two-sample t tests and linear regression models to assess associations between NP scores and brain structure.
Main Results:
- MCI patients exhibited reduced volumes in specific left and right hippocampal subfields (presubiculum, subiculum, CA2_3, CA4_DG) compared to NC.
- Volumes of these atrophied regions positively correlated with NP scores.
- These associations were dependent on cognitive status (MCI vs. NC) but not on APOE ε4 genotype; left subiculum and presubiculum volumes correlated with MoCA scores specifically in MCI patients.
Conclusions:
- Hippocampal subfield atrophy serves as a significant indicator in individuals with mild cognitive impairment.
- These structural changes are linked to cognitive performance, highlighting their potential as a sensitive biomarker for MCI.
- Findings suggest hippocampal subfield atrophy is a valuable biomarker for MCI, particularly within the Chinese population.
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