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Differential cortical atrophy in subgroups of mild cognitive impairment
Sandra Bell-McGinty1, Oscar L Lopez, Carolyn Cidis Meltzer
1Department of Psychiatry, University of Pittsburgh Medical Center, PA, USA.
Objective:
To compare gray matter brain volumes in patients diagnosed with subtypes of mild cognitive impairment (MCI) (those with a focal amnestic disorder and those with more diffuse cognitive dysfunction) with those of elderly controls.
Design:
Magnetic resonance imaging volumetric study of MCI subgroups (MCI-amnestic [MCI-A], and MCI-multiple cognitive domain [MCI-MCD]) using a whole brain voxel-based analysis.
Setting:
Referral dementia clinic. Patients Thirty-seven patients with MCI (age range, 49-85 years; MCI-A, n = 9; MCI-MCD, n = 28) and 47 control subjects (age range, 55-81 years).
Main Outcome Measures:
Volumetric anatomical magnetic resonance imaging differences between MCI subgroups and normal controls, and between patients with MCI who progressed to dementia. Magnetic resonance imaging scans were analyzed using statistical software SPM99.
Results:
Overall, the patients with MCI had significantly decreased volume in the hippocampus and middle temporal gyrus, bilaterally, compared with control subjects. Compared with patients with MCI-MCD, patients with MCI-A had significant volume loss of the left entorhinal cortex and inferior parietal lobe. Compared with patients with MCI-A, patients with MCI-MCD had significantly reduced volume of the right inferior frontal gyrus, right middle temporal gyrus, and bilateral superior temporal gyrus. Patients with MCI who progressed to Alzheimer disease during follow-up (mean interval 2 years, maximum 4.5 years), showed greater atrophy in the left entorhinal cortex, bilateral superior temporal gyri, and right inferior frontal gyrus compared with those who did not progress.
Conclusions:
These data provide evidence of distinct brain structural abnormalities in 2 groups of patients with MCI. While both have mesial temporal and cortical volume loss, those with a focal memory deficit have more involvement of the mesial temporal structures and less involvement of the neocortical heteromodal association areas than those patients with MCI with diffuse cognitive dysfunction. Thus, MCI may represent a more heterogeneous group than currently conceived, possibly reflecting 2 different etiological processes to dementia. These data also suggest that these structural abnormalities precede the development of Alzheimer disease.
Insights
Mild cognitive impairment (MCI) subtypes show distinct brain volume differences. MCI-amnestic patients exhibit mesial temporal lobe atrophy, while MCI-multiple cognitive domain patients show more widespread cortical loss, suggesting different dementia pathways.
Area of Science:
- Neuroimaging
- Neurology
- Gerontology
Background:
- Mild cognitive impairment (MCI) is a transitional stage between normal aging and dementia.
- Subtyping MCI is crucial for understanding underlying pathologies and predicting progression.
- Distinguishing between amnestic and multiple-domain MCI may reveal different neurodegenerative processes.
Purpose of the Study:
- To compare gray matter brain volumes in subtypes of mild cognitive impairment (MCI) with elderly controls.
- To investigate structural differences between MCI-amnestic (MCI-A) and MCI-multiple cognitive domain (MCI-MCD) patients.
- To identify brain regions associated with MCI progression to Alzheimer's disease.
Main Methods:
- Volumetric magnetic resonance imaging (MRI) was used for whole-brain voxel-based analysis.
- Thirty-seven MCI patients (MCI-A, n=9; MCI-MCD, n=28) and 47 controls were studied.
- Statistical Parametric Mapping (SPM99) software analyzed MRI scans.
Main Results:
- MCI patients showed reduced hippocampal and middle temporal gyrus volumes compared to controls.
- MCI-A patients had greater volume loss in the left entorhinal cortex and inferior parietal lobe than MCI-MCD patients.
- MCI-MCD patients exhibited reduced volume in the right inferior frontal gyrus, right middle temporal gyrus, and bilateral superior temporal gyri compared to MCI-A patients.
- Progression to Alzheimer's disease was associated with greater atrophy in specific cortical and mesial temporal regions.
Conclusions:
- Distinct patterns of brain structural abnormalities exist in MCI subtypes.
- MCI-A is characterized by mesial temporal and some neocortical loss, while MCI-MCD shows more diffuse neocortical involvement.
- MCI heterogeneity may reflect different etiological pathways to dementia, potentially preceding Alzheimer's disease development.
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