Cerebrospinal fluid markers for Alzheimer's disease in a cognitively healthy cohort of young and old adults

被引:27
|
作者
Paternico, Donata [1 ]
Galluzzi, Samantha [1 ]
Drago, Valeria [1 ]
Bocchio-Chiavetto, Luisella [2 ]
Zanardini, Roberta [2 ]
Pedrini, Laura [3 ]
Baronio, Manuela [4 ]
Amicucci, Giovanni [4 ]
Frisoni, Giovanni B. [1 ]
机构
[1] IRCCS San Giovanni di Dio Fatebenefratelli, LENITEM Lab Epidemiol Neuroimaging & Telemed, Brescia, Italy
[2] IRCCS San Giovanni di Dio Fatebenefratelli, Neuropsychopharmacol Unit, Brescia, Italy
[3] IRCCS San Giovanni di Dio Fatebenefratelli, Psychiat Unit, Brescia, Italy
[4] S Orsola Fatebenefratelli Hosp, Anesthesiol Serv, Brescia, Italy
关键词
Cerebrospinal fluid; Biomarkers; Alzheimer's disease; Age; Apolipoprotein E; Healthy adult; RISK-FACTORS; TAU; BIOMARKERS; AGE; DECLINE; ESTABLISHMENT; POPULATION; IMPAIRMENT; DIAGNOSIS; DEMENTIA;
D O I
10.1016/j.jalz.2011.10.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Low amyloid beta(42) (A beta(42)) and high total tau and phosphorylated tau (p-tau) concentrations in the cerebrospinal fluid (CSF) are biomarkers of Alzheimer's disease (AD), reflecting brain deposition of amyloid plaques and tangles. Age and apolipoprotein E allele E4 are two strong risk factors for AD, but few data are still available on their effect on CSF markers in normal aging. Objective: To study the effect of age on CSF A beta(42), total tau, and p-tau levels in a well-characterized group of cognitively normal subjects. Methods: CSF A beta(42) levels of 81 subjects (27% female, 53 +/- 15.3 years, range: 21-88) were determined with sandwich enzyme-linked immunosorbent assay; of these, total tau and p-tau levels were measured in 61 (75%) and 42 (52%) cases, respectively. A linear regression analysis between age and CSF markers was carried out on the whole sample and separately in apolipoprotein E allele epsilon 4 carriers and noncarriers. Results: The median levels of all markers were significantly different between young (<65 years) and old (>= 65 years) subjects (A beta(42): P = .03; tau: P = .02; p-tau: P = .002; tau/A beta(42): P = .004; p-tau/A beta(42): P = .03). The association of marker levels with age was confirmed in linear regression models, where a positive relationship with age was observed for total tau (B = 2.3; 95% confidence interval [CI]: 0.89 to 3.7; P = .002), p-tau (B = 0.5; 95% CI: 0.1 to 0.9; P = .02), and tau/A beta(42) ratio (B = 0.006; 95% CI: 0.002 to 0.01; P = .002). No subjects showed abnormal tau, whereas 19% showed abnormal CSF A beta(42) concentrations. Conclusion: In cognitively normal subjects, the concentrations of CSF biomarkers of AD are associated with age. Further longitudinal studies could clarify whether A beta(42) low levels represent a preclinical AD biomarker. (C) 2012 The Alzheimer's Association. All rights reserved.
引用
收藏
页码:520 / 527
页数:8
相关论文
共 50 条
  • [11] Homocysteine Metabolism and Cerebrospinal Fluid Markers for Alzheimer's Disease
    Popp, Julius
    Lewczuk, Piotr
    Linnebank, Michael
    Cvetanovska, Gabriela
    Smulders, Yvo
    Koelsch, Heike
    Frommann, Ingo
    Kornhuber, Johannes
    Maier, Wolfgang
    Jessen, Frank
    JOURNAL OF ALZHEIMERS DISEASE, 2009, 18 (04) : 819 - 828
  • [12] Cerebrospinal fluid oxidative stress markers in Alzheimer's disease
    Sakakibara, Ryuji
    Kawai, Takayuki
    NEUROLOGY AND CLINICAL NEUROSCIENCE, 2020, 8 (05): : 232 - 240
  • [13] Cerebrospinal fluid biomarkers of Alzheimer's disease in healthy elderly
    Randall, Catherine
    Mosconi, Lisa
    De Leon, Mony
    Glodzik, Lidia
    FRONTIERS IN BIOSCIENCE-LANDMARK, 2013, 18 : 1150 - 1173
  • [14] White matter integrity is associated with cerebrospinal fluid markers of Alzheimer's disease in normal adults
    Gold, Brian T.
    Zhu, Zude
    Brown, Christopher A.
    Andersen, Anders H.
    Ladu, Mary Jo
    Tai, Leon
    Jicha, Greg A.
    Kryscio, Richard J.
    Estus, Steven
    Nelson, Peter T.
    Scheff, Steve W.
    Abner, Erin
    Schmitt, Frederick A.
    Van Eldik, Linda J.
    Smith, Charles D.
    NEUROBIOLOGY OF AGING, 2014, 35 (10) : 2263 - 2271
  • [15] Association between Fine Particulate Matter Exposure and Cerebrospinal Fluid Biomarkers of Alzheimer ' s Disease among a Cognitively Healthy Population-Based Cohort
    Casey, Emma
    Li, Zhenjiang
    Liang, Donghai
    Ebelt, Stefanie
    Levey, Allan I.
    Lah, James J.
    Wingo, Thomas S.
    Huls, Anke
    ENVIRONMENTAL HEALTH PERSPECTIVES, 2024, 132 (04)
  • [16] Klotho in the cerebrospinal fluid of adults with and without Alzheimer's disease
    Semba, Richard D.
    Moghekar, Abhay R.
    Hu, Jason
    Sun, Kai
    Turner, Randi
    Ferrucci, Luigi
    O'Brien, Richard
    NEUROSCIENCE LETTERS, 2014, 558 : 37 - 40
  • [17] Cerebrospinal fluid biomarkers for Alzheimer's and vascular disease vary by age, gender, and APOE genotype in cognitively normal adults
    Ge Li
    Jane B. Shofer
    Eric C. Petrie
    Chang-En Yu
    Charles W. Wilkinson
    Dianne P. Figlewicz
    Andrew Shutes-David
    Jing Zhang
    Thomas J. Montine
    Murray A. Raskind
    Joseph F. Quinn
    Douglas R. Galasko
    Elaine R. Peskind
    Alzheimer's Research & Therapy, 9
  • [18] Cerebrospinal fluid biomarkers for Alzheimer's and vascular disease vary by age, gender, and APOE genotype in cognitively normal adults
    Li, Ge
    Shofer, Jane B.
    Petrie, Eric C.
    Yu, Chang-En
    Wilkinson, Charles W.
    Figlewicz, Dianne P.
    Shutes-David, Andrew
    Zhang, Jing
    Montine, Thomas J.
    Raskind, Murray A.
    Quinn, Joseph F.
    Galasko, Douglas R.
    Peskind, Elaine R.
    ALZHEIMERS RESEARCH & THERAPY, 2017, 9
  • [19] Social Networks and Cerebrospinal Fluid Biomarkers of Alzheimer's Disease Pathology in Cognitively Intact Older Adults: The CABLE Study
    Ma, Ya-Hui
    Wang, Ya-Yu
    Tan, Lan
    Xu, Wei
    Shen, Xue-Ning
    Wang, Hui-Fu
    Hou, Xiao-He
    Cao, Xi-Peng
    Bi, Yan-Lin
    Dong, Qiang
    Yang, Jiu-Long
    Yu, Jin-Tai
    JOURNAL OF ALZHEIMERS DISEASE, 2021, 81 (01) : 263 - 272
  • [20] Alzheimer's disease - Markers in the cerebrospinal fluid in support of the pathogenic hypotheses
    Blain, H
    Jeandel, C
    PRESSE MEDICALE, 1998, 27 (15): : 731 - 738