Damage to white matter networks resulting from small vessel disease and the effects on cognitive function

小血管疾病导致的白质网络损伤及其对认知功能的影响

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Abstract

White matter hyperintensities (WMHs) are prevalent in older age and are associated with cognitive decline. The location and extent of WMHs likely influences the relationship with behavior. Identifying which tracts are more likely impacted by WMHs might enable better understanding of which behaviors are affected. Therefore, this study aimed to i) identify which white matter tracts are most affected by WMHs, and ii) identify tracts where the presence of WMHs is associated with poorer cognitive scores. Participants (N = 212, 20-80 years) completed the Montreal Cognitive Assessment (MoCA). WMHs were manually delineated on FLAIR scans. In DSIStudio, we used the Human Connectome Project 1065FIB template to track how many fibers of each white matter tract intersected each participant's WMH map. Values obtained represent disconnection associated with WMHs. These scores were correlated with age, MoCA total and memory index scores. There was significantly more disconnection with older age in the right arcuate fasciculus, extreme capsule, frontal aslant tract, bilateral inferior, middle and superior longitudinal fasciculi, and the corpus callosum. Disconnection associated with WMHs in the right superior longitudinal fasciculus was significantly associated with a lower MoCA scores. Finally, disconnection in the right extreme capsule, middle and superior longitudinal fascicli, and bilateral frontal aslant tracts were significantly associated with lower MoCA memory index scores. This study highlights the prevalence of WMHs across the lifespan and demonstrates a clear relationship between tract-specific WMHs and cognition. Age-related white-matter degeneration was pronounced in many association fibers, particularly in the right hemisphere. These data suggest age related disruption of specific white matter tracts represents a clear and present risk factor for global cognition and memory as we age.

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