Evidence of altered phosphatidylcholine metabolism in Alzheimer's disease

被引:225
作者
Whiley, Luke [1 ,2 ]
Sen, Arundhuti [1 ,2 ]
Heaton, James [3 ]
Proitsi, Petroula [1 ,2 ]
Garcia-Gomez, Diego [4 ]
Leung, Rufina [1 ,2 ]
Smith, Norman [3 ]
Thambisetty, Madhav [5 ]
Kloszewska, Iwona [6 ]
Mecocci, Patrizia [7 ]
Soininen, Hilkka [8 ,9 ]
Tsolaki, Magda [10 ]
Vellas, Bruno [11 ]
Lovestone, Simon [1 ,2 ]
Legido-Quigley, Cristina [1 ,2 ]
机构
[1] Kings Coll London, Inst Pharmaceut Sci, London SE1 9NH, England
[2] Kings Coll London, Inst Psychiat, London SE1 9NH, England
[3] Kings Coll London, Waters Ctr Innovat, London SE1 9NH, England
[4] Univ Salamanca, Dept Analyt Chem, E-37008 Salamanca, Spain
[5] NIA, Clin & Tanslat Neurosci Unit, Lab Behav Neurosci, Baltimore, MD 21224 USA
[6] Med Univ Lodz, Dept Old Age Psychiat & Psychot Disorders, Lodz, Poland
[7] Univ Perugia, Dept Clin & Expt Med, Sect Gerontol & Geriatr, I-06100 Perugia, Italy
[8] Univ Eastern Finland, Dept Neurol, Kuopio, Finland
[9] Kuopio Univ Hosp, SF-70210 Kuopio, Finland
[10] Aristotle Univ Thessaloniki, Dept Neurol 3, GR-54006 Thessaloniki, Greece
[11] Hop Toulouse, Dept Internal & Geriatr Med, Toulouse, France
关键词
Alzheimer's disease; Phosphatidylcholine; ApoE; Lipid; Plasma; Mild cognitive impairment; Addneuromed; PHOSPHOLIPASE A(2) ACTIVITY; PLASMA; BIOMARKERS; LIPIDS; PROGRESSION; IDENTIFICATION; SPECTROSCOPY; ASSOCIATION; DISCOVERY; ENZYMES;
D O I
10.1016/j.neurobiolaging.2013.08.001
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Abberant lipid metabolism is implicated in Alzheimer'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 < 0.001), 16:0/22: 6 (p < 0.05), and 18: 0/22: 6 (p < 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. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:271 / 278
页数:8
相关论文
共 49 条
  • [1] Alzheimers Assoc, 1998, NEUROBIOL AGING, V19, P109
  • [2] APOE genotype effects on Alzheimer's disease onset and epidemiology
    Ashford, JW
    [J]. JOURNAL OF MOLECULAR NEUROSCIENCE, 2004, 23 (03) : 157 - 165
  • [3] Using biomarkers to improve detection of Alzheimer's disease
    Biagioni, Milton C.
    Galvin, James E.
    [J]. NEURODEGENERATIVE DISEASE MANAGEMENT, 2011, 1 (02) : 127 - 139
  • [4] Elevated 4-hydroxyhexenal in Alzheimer's disease (AD) progression
    Bradley, Melissa A.
    Xiong-Fister, Shuling
    Markesbery, William R.
    Lovell, Mark A.
    [J]. NEUROBIOLOGY OF AGING, 2012, 33 (06) : 1034 - 1044
  • [5] Metabolic Signatures of Lung Cancer in Biofluids: NMR-Based Metabonomics of Urine
    Carrola, Joana
    Rocha, Claudia M.
    Barros, Antonio S.
    Gil, Ana M.
    Goodfellow, Brian J.
    Carreira, Isabel M.
    Bernardo, Joao
    Gomes, Ana
    Sousa, Vitor
    Carvalho, Lina
    Duarte, Iola F.
    [J]. JOURNAL OF PROTEOME RESEARCH, 2011, 10 (01) : 221 - 230
  • [6] Gene expression profiling of 12633 genes in Alzheimer hippocampal CA1: Transcription and neurotrophic factor down-regulation and up-regulation of apoptotic and pro-inflammatory signaling
    Colangelo, V
    Schurr, J
    Ball, MJ
    Pelaez, RP
    Bazan, NG
    Lukiw, WJ
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 70 (03) : 462 - 473
  • [7] ApoE-Directed Therapeutics Rapidly Clear β-Amyloid and Reverse Deficits in AD Mouse Models
    Cramer, Paige E.
    Cirrito, John R.
    Wesson, Daniel W.
    Lee, C. Y. Daniel
    Karlo, J. Colleen
    Zinn, Adriana E.
    Casali, Brad T.
    Restivo, Jessica L.
    Goebel, Whitney D.
    James, Michael J.
    Brunden, Kurt R.
    Wilson, Donald A.
    Landreth, Gary E.
    [J]. SCIENCE, 2012, 335 (6075) : 1503 - 1506
  • [8] Phospholipase A2 Enzymes: Physical Structure, Biological Function, Disease Implication, Chemical Inhibition, and Therapeutic Intervention
    Dennis, Edward A.
    Cao, Jian
    Hsu, Yuan-Hao
    Magrioti, Victoria
    Kokotos, George
    [J]. CHEMICAL REVIEWS, 2011, 111 (10) : 6130 - 6185
  • [9] Linking lipids to Alzheimer's disease: cholesterol and beyond
    Di Paolo, Gilbert
    Kim, Tae-Wan
    [J]. NATURE REVIEWS NEUROSCIENCE, 2011, 12 (05) : 284 - 296
  • [10] Identification of metabolites in human hepatic bile using 800 MHz 1H NMR spectroscopy, HPLC-NMR/MS and UPLC-MS
    Duarte, Iola F.
    Legido-Quigley, Cristina
    Parker, David A.
    Swann, Jonathan R.
    Spraul, Manfred
    Braumann, Ulrich
    Gil, Ana M.
    Holmes, Elaine
    Nicholson, Jeremy K.
    Murphy, Gerard M.
    Vilca-Melendez, Hector
    Heatond, Nigel
    Lindon, John C.
    [J]. MOLECULAR BIOSYSTEMS, 2009, 5 (02) : 180 - 190