The future of blood-based biomarkers for Alzheimer's disease

被引:235
作者
Henriksen, Kim [1 ]
O'Bryant, Sid E. [2 ]
Hamper, Harald [3 ]
Trojanowski, John Q. [4 ]
Montine, Thomas J. [5 ]
Jeromin, Andreas [6 ]
Blennow, Kaj [7 ]
Lonneborg, Anders [8 ]
Wyss-Coray, Tony [9 ]
Soares, Holly [10 ]
Bazenet, Chantal [11 ]
Sjogren, Magnus [8 ]
Hu, William [12 ]
Lovestone, Simon [11 ]
Karsdal, Morten A. [1 ]
Weiner, Michael W. [13 ,14 ,15 ,16 ]
机构
[1] Nord Biosci Biomarkers & Res, Neurodegenerat Dis, Herlev, Denmark
[2] Univ N Texas, Hlth Sci Ctr, Dept Internal Med, Ft Worth, TX USA
[3] Goethe Univ Frankfurt, Dept Psychiat, D-60054 Frankfurt, Germany
[4] Univ Penn, Dept Pathol & Lab Med, Ctr Neurodegenerat Dis Res,Inst Aging,Perelman Sc, Alzheimers Dis Core Ctr,Udall Parkinsons Res Ctr, Philadelphia, PA USA
[5] Univ Washington, Dept Pathol, Seattle, WA 98195 USA
[6] NextGen Sci, Ann Arbor, MI USA
[7] Univ Goteborg, Sahlgrenska Univ Hosp, Dept Neurosci & Physiol, Clin Neurochem Lab, Molndal, Sweden
[8] DiaGenic ASA, Oslo, Norway
[9] Stanford Univ, Sch Med, Dept Neurol & Neurol Sci, Stanford, CA 94305 USA
[10] Bristol Myers Squibb Co, Wallingford, CT 06492 USA
[11] Kings Coll London, Inst Psychiat, Dept Old Age Psychiat, London, England
[12] Emory Univ, Sch Med, Dept Neurol, Ctr Neurodegenerat Dis Res, Atlanta, GA 30322 USA
[13] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[14] Univ Calif San Francisco, Dept Radiol, San Francisco, CA USA
[15] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA USA
[16] Univ Calif San Francisco, Dept Neurol, San Francisco, CA USA
基金
美国国家卫生研究院; 瑞典研究理事会;
关键词
Blood; Plasma; Serum; Biomarkers; Alzheimer's disease; PLASMA AMYLOID-BETA; CEREBROSPINAL-FLUID; ALPHA-SYNUCLEIN; BIOCHEMICAL MARKERS; DIURNAL-VARIATION; INFLAMMATORY MARKERS; NATRIURETIC PEPTIDE; CASPASE-CLEAVAGE; APOLIPOPROTEIN-E; TAU PROTEINS;
D O I
10.1016/j.jalz.2013.01.013
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Treatment of Alzheimer's disease (AD) is significantly hampered by the lack of easily accessible biomarkers that can detect disease presence and predict disease risk reliably. Fluid biomarkers of AD currently provide indications of disease stage; however, they are not robust predictors of disease progression or treatment response, and most are measured in cerebrospinal fluid, which limits their applicability. With these aspects in mind, the aim of this article is to underscore the concerted efforts of the Blood-Based Biomarker Interest Group, an international working group of experts in the field. The points addressed include: (1) the major challenges in the development of blood-based biomarkers of AD, including patient heterogeneity, inclusion of the "right" control population, and the blood brain barrier; (2) the need for a clear definition of the purpose of the individual markers (e.g., prognostic, diagnostic, or monitoring therapeutic efficacy); (3) a critical evaluation of the ongoing biomarker approaches; and (4) highlighting the need for standardization of preanalytical variables and analytical methodologies used by the field. (C) 2014 The Alzheimer's Association. All rights reserved.
引用
收藏
页码:115 / 131
页数:17
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