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Generalized Psychophysiological Interaction (PPI) Analysis of Memory Related Connectivity in Individuals at Genetic Risk for Alzheimer's Disease
Published on: November 14, 2017
Abnormal white matter independent of hippocampal atrophy in amnestic type mild cognitive impairment
Feng Bai1, Zhijun Zhang, David R Watson
1School of Clinical Medicine, Southeast University, Nanjing 210009, China.
Abstract:
Hippocampal atrophy is the key marker in the pathogenesis of Alzheimer's disease (AD), which is associated with white matter (WM) disruption. This type of WM disruption could partly explain AD-related pathology. However, relatively little attention has been directed toward WM disruption which may be independent of these fundamental gray matter (GM) changes in amnestic mild cognitive impairment (aMCI) which is associated with high risk of AD. To evaluate the differences of WM integrity between aMCI patients (N=32) and healthy controls (N=31), whole-brain voxel-based methods were applied to diffusion tensor imaging. To explore the possible independence of WM changes from GM loss, an index of hippocampal atrophy was used to partial out GM effects. aMCI patients showed WM disruption in frontal lobe, temporal lobe, internal capsule, cingulate gyrus and precuneus. The findings supported the evidence of independent patterns of degeneration in WM tracts which may co-act in the WM pathological process of aMCI patients. As aMCI is a putatively prodromal syndrome to AD, these data may assist with a better understanding of WM pathological change associated with the development of AD.
Insights
White matter disruption is evident in amnestic mild cognitive impairment (aMCI) and may occur independently of gray matter loss. These findings offer insights into early Alzheimer's disease (AD) pathology.
Area of Science:
- Neuroimaging
- Neurology
- Biomedical Science
Background:
- Hippocampal atrophy is a key marker in Alzheimer's disease (AD) pathogenesis, linked to white matter (WM) disruption.
- White matter changes may contribute to AD pathology, but their independence from gray matter (GM) changes in amnestic mild cognitive impairment (aMCI) is less understood.
Purpose of the Study:
- To evaluate differences in WM integrity between aMCI patients and healthy controls.
- To explore whether WM disruption in aMCI is independent of GM loss, specifically hippocampal atrophy.
Main Methods:
- Whole-brain voxel-based analysis of diffusion tensor imaging (DTI) data.
- Used an index of hippocampal atrophy to partial out GM effects.
- Compared WM integrity in 32 aMCI patients and 31 healthy controls.
Main Results:
- aMCI patients exhibited significant WM disruption in the frontal lobe, temporal lobe, internal capsule, cingulate gyrus, and precuneus.
- Evidence suggests independent patterns of WM degeneration in aMCI.
- WM changes were observed even after accounting for hippocampal atrophy.
Conclusions:
- WM disruption in aMCI can be independent of GM atrophy.
- These findings enhance understanding of WM pathological changes in aMCI, a prodromal stage of AD.
- Independent WM degeneration patterns may co-exist in the WM pathological process of aMCI.
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