Fluid Biomarkers in Alzheimer Disease

被引:141
作者
Blennow, Kaj [1 ]
Zetterberg, Henrik [1 ]
Fagan, Anne M. [2 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Sahlgrenska Univ Hosp, Inst Neurosci & Physiol,Clin Neurochem Lab,Dept P, SE-43180 Molndal, Sweden
[2] Washington Univ, Sch Med, Charles F & Joanne Knight Alzheimers Dis Res Ctr, Dept Neurol,Hope Ctr Neurol Disorders, St Louis, MO 63110 USA
来源
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE | 2012年 / 2卷 / 09期
关键词
MILD COGNITIVE IMPAIRMENT; HUMAN CEREBROSPINAL-FLUID; AMYLOID PRECURSOR PROTEIN; GAMMA-SECRETASE INHIBITOR; PHOSPHORYLATED TAU-PROTEIN; CSF BIOMARKERS; A-BETA; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE;
D O I
10.1101/cshperspect.a006221
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Research progress has provided detailed understanding of the molecular pathogenesis of Alzheimer disease (AD). This knowledge has been translated into new drug candidates with putative disease-modifying effects, which are now being tested in clinical trials. The promise of effective therapy has created a great need for biomarkers able to detect AD in the predementia phase, because drugs will probably be effective only if neurodegeneration is not too advanced. In this chapter, cerebrospinal fluid (CSF) and plasma biomarkers are reviewed. The core CSF biomarkers total tau (T-tau), phosphorylated tau (P-tau) and the 42 amino acid form of beta-amyloid (A beta 42) reflect AD pathology, and have high diagnostic accuracy to diagnose AD with dementia and prodromal AD in mild cognitive impairment cases. The rationale for the use of CSF biomarkers to identify and monitor the mechanism of action of new drug candidates is also outlined in this chapter.
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页数:23
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