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Plasma lipids metabolism in mild cognitive impairment and Alzheimer's disease.

Authors :
Costa AC
Joaquim HPG
Forlenza O
Talib LL
Gattaz WF
Source :
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry [World J Biol Psychiatry] 2019 Mar; Vol. 20 (3), pp. 190-196. Date of Electronic Publication: 2017 Sep 19.
Publication Year :
2019

Abstract

Objectives: Expression of phospholipids and related molecules could provide panels of multiple biomarkers searching for the signature of Alzheimer's disease (AD). The aim of the present study was to quantify ten phospholipids and simultaneously determine phospholipase A <subscript>2</subscript> (PLA <subscript>2</subscript> ) activity in blood of mild cognitive impairment (MCI) and AD patients.<br />Methods: Thirty-four AD, 20 MCI and 25 controls were enrolled. The phospholipids where analysed using the AbsoluteIDQ <superscript>®</superscript> p180 Kit. PLA <subscript>2</subscript> activities were accessed in platelets by a radio-enzymatic assay.<br />Results: The study failed to fix the ten phospholipids as a panel to predict AD; the levels of PCaaC36:6, PCaaC40:6 and C16:1-OH were lower in MCI than in controls (P = 0.041, P = 0.012, P = 0.044 respectively). PCaaC40:2 levels were lower in MCI than in AD (P = 0.041). The converters MCI-AD showed at baseline lower levels of PCaaC40:2 (P = 0.050) and PCaaC40:6 (P = 0.037) than controls. iPLA <subscript>2</subscript> activity was reduced in AD and MCI than in controls (P < 0.001). We found positive correlation in the control group between PCaaC38:6 and tPLA <subscript>2</subscript> (r = 0.680; P = 0.001) and sPLA <subscript>2</subscript> (r = 0.601; P = 0.004); PCaaC40:1 and iPLA <subscript>2</subscript> (r = 0.503; P = 0.020); PCaaC40:6 and tPLA <subscript>2</subscript> (r = 0.532; P = 0.013) and sPLA <subscript>2</subscript> (r = 0.523; P = 0.015).<br />Conclusions: Lipids metabolites in plasma might indirectly indicate changes in neuronal membrane and this deregulation can outline the transition between healthy and diseased brains.

Details

Language :
English
ISSN :
1814-1412
Volume :
20
Issue :
3
Database :
MEDLINE
Journal :
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry
Publication Type :
Academic Journal
Accession number :
28922966
Full Text :
https://doi.org/10.1080/15622975.2017.1369566