Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.neurobiolaging.2014.02.025
Title: The brain lipidomes of subcortical ischemic vascular dementia and mixed dementia
Authors: Lam, Sin Man
Wang, Yuting 
Duan, Xinrui 
Wenk, Markus R 
Kalaria, Raj N
Chen, Christopher P 
Lai, Mitchell KP 
Shui, Guanghou 
Keywords: Science & Technology
Life Sciences & Biomedicine
Geriatrics & Gerontology
Neurosciences
Neurosciences & Neurology
Lipidomics
Subcortical ischemic vascular dementia
Mixed dementia
Alzheimer's disease
Sphingolipids
Phospholipids
Mass spectrometry
EARLY ALZHEIMERS-DISEASE
NERVOUS-SYSTEM
WHITE-MATTER
FATTY-ACIDS
PATHOGENESIS
MEMBRANE
PHOSPHOLIPIDS
SPECTROMETRY
DEFICIENCY
EXPRESSION
Issue Date: 1-Oct-2014
Publisher: ELSEVIER SCIENCE INC
Citation: Lam, Sin Man, Wang, Yuting, Duan, Xinrui, Wenk, Markus R, Kalaria, Raj N, Chen, Christopher P, Lai, Mitchell KP, Shui, Guanghou (2014-10-01). The brain lipidomes of subcortical ischemic vascular dementia and mixed dementia. NEUROBIOLOGY OF AGING 35 (10) : 2369-2381. ScholarBank@NUS Repository. https://doi.org/10.1016/j.neurobiolaging.2014.02.025
Abstract: Despite its importance as the leading cause of vascular dementia, the primary pathogenic mechanisms in subcortical ischemic vascular dementia (SIVD) have remained elusive. Because of the lack of approved therapeutic agents for SIVD, there is a pressing need to identify novel therapeutic targets. Comparative lipidomic analyses of SIVD and mixed dementia (i.e., SIVD and Alzheimer's disease, MixD) may also confer new insights pertaining to the possible interaction between neurodegenerative and vascular mechanisms in the pathogenesis of dementia. Liquid chromatography coupled to mass spectrometry was used to comprehensively analyze the lipidomes of white and gray matter from the temporal cortex of nondemented controls, SIVD, and MixD subjects. Detailed molecular profiles highlighted the pathologic relevance of gray matter sphingolipid fatty acyl chain heterogeneity in dementia. In addition, the levels of sulfatides and lysobisphosphatidic acids were progressively increased in the temporal cortex gray matter from control to SIVD to MixD. White matter phospholipid profiles indicated possible adaptive mechanisms (i.e., increased unsaturation) to chronic ischemia in SIVD and elevated membrane degradation in MixD. © 2014 The Authors.
Source Title: NEUROBIOLOGY OF AGING
URI: https://scholarbank.nus.edu.sg/handle/10635/188460
ISSN: 01974580
15581497
DOI: 10.1016/j.neurobiolaging.2014.02.025
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