Cerebrovascular disease, neurodegeneration, and clinical phenotype in dementia with Lewy bodies
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
R01 AG041851
NIA NIH HHS - United States
C06 RR018898
NCRR NIH HHS - United States
P50 AG016574
NIA NIH HHS - United States
R01 AG040042
NIA NIH HHS - United States
Department of Health - United Kingdom
R01 AG011378
NIA NIH HHS - United States
R01 NS080820
NINDS NIH HHS - United States
P30 AG062677
NIA NIH HHS - United States
R37 AG011378
NIA NIH HHS - United States
U01 NS100620
NINDS NIH HHS - United States
U01 AG006786
NIA NIH HHS - United States
PubMed
34130107
PubMed Central
PMC8338792
DOI
10.1016/j.neurobiolaging.2021.04.029
PII: S0197-4580(21)00153-6
Knihovny.cz E-resources
- Keywords
- Cerebrovascular disease, Dementia with Lewy bodies (DLB), Magnetic resonance imaging, Neurodegeneration, White matter hyperintensities, infarcts,
- MeSH
- White Matter diagnostic imaging pathology MeSH
- Cerebrovascular Disorders complications MeSH
- Nerve Degeneration etiology MeSH
- Lewy Body Disease diagnostic imaging etiology pathology psychology MeSH
- Hallucinations MeSH
- Cognition MeSH
- Middle Aged MeSH
- Humans MeSH
- Magnetic Resonance Imaging MeSH
- Cerebral Cortex blood supply diagnostic imaging pathology MeSH
- Brain Infarction diagnostic imaging pathology MeSH
- REM Sleep Behavior Disorder etiology MeSH
- Gray Matter diagnostic imaging pathology MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
We investigated whether cerebrovascular disease contributes to neurodegeneration and clinical phenotype in dementia with Lewy bodies (DLB). Regional cortical thickness and subcortical gray matter volumes were estimated from structural magnetic resonance imaging (MRI) in 165 DLB patients. Cortical and subcortical infarcts were recorded and white matter hyperintensities (WMHs) were assessed. Subcortical only infarcts were more frequent (13.3%) than cortical only infarcts (3.1%) or both subcortical and cortical infarcts (2.4%). Infarcts, irrespective of type, were associated with WMHs. A higher WMH volume was associated with thinner orbitofrontal, retrosplenial, and posterior cingulate cortices, smaller thalamus and pallidum, and larger caudate volume. A higher WMH volume was associated with the presence of visual hallucinations and lower global cognitive performance, and tended to be associated with the absence of probable rapid eye movement sleep behavior disorder. Presence of infarcts was associated with the absence of parkinsonism. We conclude that cerebrovascular disease is associated with gray matter neurodegeneration in patients with probable DLB, which may have implications for the multifactorial treatment of probable DLB.
Day Hospital of Geriatrics Memory Resource and Research Centre ICONE Strasbourg France
Department of Health Sciences Mayo Clinic Rochester MN USA
Department of Neurology and Alzheimer Center VU University Medical Center Amsterdam Netherlands
Department of Neurology Mayo Clinic Jacksonville FL USA
Department of Neurology Mayo Clinic Rochester MN USA
Department of Psychiatry and Psychology Mayo Clinic Jacksonville FL
Department of Psychiatry and Psychology Mayo Clinic Rochester MN USA
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