Austin Health

Title
Relationships Between Plasma Lipids Species, Gender, Risk Factors, and Alzheimer's Disease.
Publication Date
2020
Author(s)
Lim, Wei Ling Florence
Huynh, Kevin
Chatterjee, Pratishtha
Martins, Ian
Jayawardana, Kaushala S
Giles, Corey
Mellett, Natalie A
Laws, Simon M
Bush, Ashley I
Rowe, Christopher C
Villemagne, Victor L
Ames, David
Drew, Brian G
Masters, Colin L
Meikle, Peter J
Martins, Ralph N
Subject
APOEɛ4
Aging
Alzheimer’s disease
gender
lipid species
Type of document
Journal Article
DOI
10.3233/JAD-191304
Abstract
Lipid metabolism is altered in Alzheimer's disease (AD); however, the relationship between AD risk factors (age, APOEɛ4, and gender) and lipid metabolism is not well defined. We investigated whether altered lipid metabolism associated with increased age, gender, and APOE status may contribute to the development of AD by examining these risk factors in healthy controls and also clinically diagnosed AD individuals. We performed plasma lipidomic profiling (582 lipid species) of the Australian Imaging, Biomarkers and Lifestyle flagship study of aging cohort (AIBL) using liquid chromatography-mass spectrometry. Linear regression and interaction analysis were used to explore the relationship between risk factors and plasma lipid species. We observed strong associations between plasma lipid species with gender and increasing age in cognitively normal individuals. However, APOEɛ4 was relatively weakly associated with plasma lipid species. Interaction analysis identified differential associations of sphingolipids and polyunsaturated fatty acid esterified lipid species with AD based on age and gender, respectively. These data indicate that the risk associated with age, gender, and APOEɛ4 may, in part, be mediated by changes in lipid metabolism. This study extends our existing knowledge of the relationship between the lipidome and AD and highlights the complexity of the relationships between lipid metabolism and AD at different ages and between men and women. This has important implications for how we assess AD risk and also for potential therapeutic strategies involving modulation of lipid metabolic pathways.
Link
Citation
Journal of Alzheimer's Disease : JAD 2020; 76(1): 303-315
Jornal Title
Journal of Alzheimer's Disease : JAD

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