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Evidence of altered phosphatidylcholine metabolism in Alzheimer's disease

Authors :
Whiley, L.
Sen, A.
Heaton, J.
Proitsi, P.
García-Gómez, D.
Leung, R.
Smith, N.
Thambisetty, M.
Kloszewska, I.
Mecocci, P.
Soininen, H.
Tsolaki, M.
Vellas, B.
Lovestone, S.
Legido-Quigley, C.
Whiley, L.
Sen, A.
Heaton, J.
Proitsi, P.
García-Gómez, D.
Leung, R.
Smith, N.
Thambisetty, M.
Kloszewska, I.
Mecocci, P.
Soininen, H.
Tsolaki, M.
Vellas, B.
Lovestone, S.
Legido-Quigley, C.
Source :
Whiley, L. <
Publication Year :
2014

Abstract

Abberant lipid metabolism is implicated in Alzheimer&#39;s disease (AD) pathophysiology, but the connections between AD and lipid metabolic pathways are not fully understood. To investigate plasma lipids in AD, a multiplatform screen (n = 35 by liquid chromatography–mass spectrometry and n = 35 by nuclear magnetic resonance) was developed, which enabled the comprehensive analysis of plasma from 3 groups (individuals with AD, individuals with mild cognitive impairment (MCI), and age-matched controls). This screen identified 3 phosphatidylcholine (PC) molecules that were significantly diminished in AD cases. In a subsequent validation study (n = 141), PC variation in a bigger sample set was investigated, and the same 3 PCs were found to be significantly lower in AD patients: PC 16:0/20:5 (p &lt; 0.001), 16:0/22:6 (p &lt; 0.05), and 18:0/22:6 (p &lt; 0.01). A receiver operating characteristic (ROC) analysis of the PCs, combined with apolipoprotein E (ApoE) data, produced an area under the curve predictive value of 0.828. Confirmatory investigations into the background biochemistry indiciated no significant change in plasma levels of 3 additional PCs of similar structure, total choline containing compounds or total plasma omega fatty acids, adding to the evidence that specific PCs play a role in AD pathology.

Details

Database :
OAIster
Journal :
Whiley, L. <
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1150889890
Document Type :
Electronic Resource