White matter lesions

Autor: Hans J. Grabe, Mohamad Habes, Deborah Janowitz, Guray Erus, Aristeidis Sotiras, David A. Wolk, Christos Davatzikos, Wolfgang Hoffmann, Jimit Doshi, Nick Bryan, Jon B. Toledo, Susan M. Resnick, Ulf Schminke, Haochang Shou, Henry Völzke
Rok vydání: 2018
Předmět:
Male
0301 basic medicine
Aging
Longitudinal study
Trail Making Test
genetics [Leukoencephalopathies]
genetics [Alzheimer Disease]
diagnostic imaging [Cognition Disorders]
pathology [Alzheimer Disease]
pathology [Aging]
0302 clinical medicine
Leukoencephalopathies
Risk Factors
Medicine
Longitudinal Studies
Young adult
Cognitive decline
Aged
80 and over

Cerebral Cortex
Genetics
Age Factors
Middle Aged
Magnetic Resonance Imaging
Study of Health in Pomerania
diagnostic imaging [Leukoencephalopathies]
Female
Alzheimer's disease
Adult
behavioral disciplines and activities
Article
Young Adult
03 medical and health sciences
Atrophy
Alzheimer Disease
Humans
ddc:610
complications [Leukoencephalopathies]
Aged
epidemiology [Leukoencephalopathies]
business.industry
etiology [Cognition Disorders]
medicine.disease
Hyperintensity
Cross-Sectional Studies
030104 developmental biology
pathology [Cerebral Cortex]
Neurology (clinical)
Cognition Disorders
business
030217 neurology & neurosurgery
Zdroj: Neurology 91(10), e964-e975 (2018). doi:10.1212/WNL.0000000000006116
ISSN: 1526-632X
0028-3878
DOI: 10.1212/wnl.0000000000006116
Popis: ObjectivesTo investigate spatial heterogeneity of white matter lesions or hyperintensities (WMH).MethodsMRI scans of 1,836 participants (median age 52.2 ± 13.16 years) encompassing a wide age range (22–84 years) from the cross-sectional Study of Health in Pomerania (Germany) were included as discovery set identifying spatially distinct components of WMH using a structural covariance approach. Scans of 307 participants (median age 73.8 ± 10.2 years, with 747 observations) from the Baltimore Longitudinal Study of Aging (United States) were included to examine differences in longitudinal progression of these components. The associations of these components with vascular risk factors, cortical atrophy, Alzheimer disease (AD) genetics, and cognition were then investigated using linear regression.ResultsWMH were found to occur nonuniformly, with higher frequency within spatially heterogeneous patterns encoded by 4 components, which were consistent with common categorizations of deep and periventricular WMH, while further dividing the latter into posterior, frontal, and dorsal components. Temporal trends of the components differed both cross-sectionally and longitudinally. Frontal periventricular WMH were most distinctive as they appeared in the fifth decade of life, whereas the other components appeared later in life during the sixth decade. Furthermore, frontal WMH were associated with systolic blood pressure and with pronounced atrophy including AD-related regions. AD polygenic risk score was associated with the dorsal periventricular component in the elderly. Cognitive decline was associated with the dorsal component.ConclusionsThese results support the hypothesis that the appearance of WMH follows age and disease-dependent regional distribution patterns, potentially influenced by differential underlying pathophysiologic mechanisms, and possibly with a differential link to vascular and neurodegenerative changes.
Databáze: OpenAIRE