Methodology for Discovery of Alzheimer's Disease Blood-Based Biomarkers

被引:30
作者
Maes, Olivier C. [3 ]
Schipper, Hyman M. [3 ,4 ,5 ]
Chertkow, Howard M. [3 ,4 ,5 ]
Wang, Eugenia [1 ,2 ]
机构
[1] Univ Louisville, Gheens Ctr Aging, Sch Med, Louisville, KY 40202 USA
[2] Univ Louisville, Dept Biochem & Mol Biol, Sch Med, Louisville, KY 40202 USA
[3] Sir Mortimer B Davis Jewish Hosp, Lady Davis Inst Med Res, Bloomfield Ctr Res Aging, Ctr Neurotranslat Res, Montreal, PQ H3T 1E2, Canada
[4] McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ, Canada
[5] McGill Univ, Dept Geriatr Med, Montreal, PQ, Canada
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2009年 / 64卷 / 06期
关键词
Bio-repository; Biomarker; Peripheral blood mononuclear cell; Sporadic Alzheimer's disease; Mild cognitive impairment; MILD COGNITIVE IMPAIRMENT; GENE-EXPRESSION; HEME OXYGENASE-1; MESSENGER-RNA; MICRORNA; PROTEIN; MICROARRAY; DIAGNOSIS; MARKERS; BRAIN;
D O I
10.1093/gerona/glp045
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
Alzheimer's disease (AD) is a degenerative brain disorder. The disease also affects peripheral tissue such as peripheral blood mononuclear cells (PBMCs). Delineating biochemical alterations in AD blood constituents may possibly allow the identification of accessible footprints that reflect degenerative processes within the central nervous system. Here, we describe an integrated methodology for the generation of a blood-based molecular bio-repository, including the collection of clinical and demographic data for downstream stringent sample selection and stratification for the Study of molecular Signatures in AD. We report the simultaneous extraction of high quality and yield of DNA, RNA, and protein from PBMCs of individuals with sporadic AD. mild cognitive impairment. and normal elderly controls. We describe experimental designs and present examples for the discovery of underlying etiopathogenetic networks in sporadic AD. We suggest that PBMC-associated biomarkers may provide insights into the pathogenesis of AD and be used to monitor disease diagnosis and progression.
引用
收藏
页码:636 / 645
页数:10
相关论文
共 79 条
[31]   Blood mononuclear cell gene expression profiles characterize the oxidant, hemolytic, and inflammatory stress of sickle cell disease [J].
Jison, ML ;
Munson, PJ ;
Barb, JJ ;
Suffredini, AF ;
Talwar, S ;
Logun, C ;
Raghavachari, N ;
Beigel, JH ;
Shelhamer, JH ;
Danner, RL ;
Gladwin, MT .
BLOOD, 2004, 104 (01) :270-280
[32]  
Kearney P, 2008, J PROTEOMICS BIOINFO, V1, P315
[33]  
Klunk WE, 1998, NEUROBIOL AGING, V19, P145, DOI 10.1016/S0197-4580(98)00013-X
[34]   Combinatorial microRNA target predictions [J].
Krek, A ;
Grun, D ;
Poy, MN ;
Wolf, R ;
Rosenberg, L ;
Epstein, EJ ;
MacMenamin, P ;
da Piedade, I ;
Gunsalus, KC ;
Stoffel, M ;
Rajewsky, N .
NATURE GENETICS, 2005, 37 (05) :495-500
[35]   Blood-sample processing for the study of age-dependent gene expression in peripheral blood mononuclear cells [J].
Lacelle, C ;
Riol, H ;
Xu, SY ;
Tang, YJ ;
Wang, YS ;
Chuang, YL ;
Lin, HS ;
Chang, MC ;
Liang, J ;
Wang, E .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2002, 57 (07) :B285-B287
[36]   Establishing lymphoblastoid cell lines from frozen blood of extremely old individuals [J].
Lacelle, C ;
Wang, E .
MECHANISMS OF AGEING AND DEVELOPMENT, 2002, 123 (10) :1415-1418
[37]   AN ANALYSIS OF LYMPHOCYTE-T SUBPOPULATIONS IN PATIENTS WITH ALZHEIMERS-DISEASE [J].
LEFFELL, MS ;
LUMSDEN, L ;
STEIGER, WA .
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 1985, 33 (01) :4-8
[38]   Micro-RNA speciation in fetal, adult and Alzheimer's disease hippocampus [J].
Lukiw, Walter J. .
NEUROREPORT, 2007, 18 (03) :297-300
[39]  
MAES OC, 2009, CURR GENOM IN PRESS
[40]   Murine microRNAs implicated in liver functions and aging process [J].
Maes, Olivier C. ;
An, Jin ;
Sarojini, Harshini ;
Wang, Eugenia .
MECHANISMS OF AGEING AND DEVELOPMENT, 2008, 129 (09) :534-541