Plasma Sphingomyelins in Late-Onset Alzheimer's Disease

被引:8
|
作者
Fote, Gianna [1 ]
Wu, Jie [1 ,2 ]
Mapstone, Mark [3 ]
Macciardi, Fabio [4 ]
Fiandaca, Massimo S. [5 ,6 ,7 ]
Federoff, Howard J. [3 ]
机构
[1] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92717 USA
[2] Univ Calif Irvine, Ctr Complex Biol Syst, Irvine, CA USA
[3] Univ Calif Irvine, Dept Neurol, Irvine, CA 92717 USA
[4] Univ Calif Irvine, Dept Psychiat & Human Behav, Irvine, CA 92717 USA
[5] Univ Calif Irvine, Dept Neurol, Translat Lab & Biorepository, Sch Med, Irvine, CA 92717 USA
[6] Univ Calif Irvine, Sch Med, Dept Neurol Surg, Irvine, CA 92717 USA
[7] Univ Calif Irvine, Dept Anat & Neurobiol, Sch Med, Irvine, CA 92717 USA
关键词
Alzheimer's disease; metabolomics; plasma; sphingolipids; sphingomyelin; MILD COGNITIVE IMPAIRMENT; SPHINGOLIPID METABOLISM; GENETIC-VARIATION; BRAIN; CERAMIDE; RISK; ASSOCIATION; PROTEIN; HIPPOCAMPUS; PROGRESSION;
D O I
10.3233/JAD-200871
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Altered plasma levels of sphingolipids, including sphingomyelins (SM), have been found in mouse models of Alzheimer's disease (AD) and in AD patient plasma samples. Objective: This study assesses fourteen plasma SM species in a late-onset AD (LOAD) patient cohort (n = 138). Methods: Specimens from control, preclinical, and symptomatic subjects were analyzed using targeted mass-spectrometrybased metabolomic methods. Results: Total plasma SM levels were not significantly affected by age or cognitive status. However, one metabolite that has been elevated in manifest AD in several recent studies, SM OHC14:1, was reduced significantly in pre-clinical AD and MCI relative to normal controls. Conclusion: We recommend additional comprehensive plasma lipidomics in experimental and clinical biospecimens related to LOAD that might advance the utility of plasma sphingomyelin levels in molecular phenotyping and interpretations of pathobiological mechanisms.
引用
收藏
页码:1161 / 1171
页数:11
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