Affiliation:
1. McConnell Brain Imaging Centre Montreal Neurological Institute McGill University Montreal Quebec Canada
2. Department of Neurology and Neurosurgery McGill University Montreal Quebec Canada
3. Department of Psychiatry McGill University Montreal Quebec Canada
4. Douglas Mental Health University Institute, McGill University Montreal Quebec Canada
Abstract
AbstractBACKGROUNDWhite matter hyperintensities (WMHs) are associated with cognitive decline and progression to mild cognitive impairment (MCI) and dementia. It remains unclear if sex differences influence WMH progression or the relationship between WMH and cognition.METHODSLinear mixed models examined the relationship between risk factors, WMHs, and cognition in males and females.RESULTSMales exhibited increased WMH progression in occipital, but lower progression in frontal, total, and deep than females. For males, history of hypertension was the strongest contributor, while in females, the vascular composite was the strongest contributor to WMH burden. WMH burden was more strongly associated with decreases in global cognition, executive functioning, memory, and functional activities in females than males.DISCUSSIONControlling vascular risk factors may reduce WMH in both males and females. For males, targeting hypertension may be most important to reduce WMHs. The results have implications for therapies/interventions targeting cerebrovascular pathology and subsequent cognitive decline.Highlights
Hypertension is the main vascular risk factor associated with WMH in males
A combination of vascular risk factors contributes to WMH burden in females
Only small WMH burden differences were observed between sexes
Females’ cognition was more negatively impacted by WMH burden than males
Females with WMHs may have less resilience to future pathology
Funder
National Institutes of Health
U.S. Department of Defense
Canadian Institutes of Health Research
Subject
Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology
Cited by
4 articles.
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